Variant report
Variant | rs11165210 |
---|---|
Chromosome Location | chr1:95143397-95143398 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:21)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:21 , 50 per page) page:
1
No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | USF2 | chr1:95143383-95143578 | GM12878 | blood: | n/a | chr1:95143518-95143529 |
2 | FOS | chr1:95143316-95143639 | K562 | blood: | n/a | n/a |
3 | USF1 | chr1:95143303-95143635 | ECC-1 | luminal epithelium: | n/a | n/a |
4 | USF2 | chr1:95143332-95143602 | K562 | blood: | n/a | chr1:95143518-95143529 |
5 | ATF3 | chr1:95143325-95143609 | K562 | blood: | n/a | n/a |
6 | USF1 | chr1:95143349-95143676 | SK-N-SH | brain: | n/a | n/a |
7 | USF1 | chr1:95143316-95143692 | A549 | lung: | n/a | n/a |
8 | USF1 | chr1:95143384-95143620 | SK-N-SH_RA | brain: | n/a | n/a |
9 | NFYB | chr1:95143377-95143584 | GM12878 | blood: | n/a | chr1:95143464-95143479 |
10 | USF2 | chr1:95143370-95143640 | Hela-S3 | cervix: | n/a | chr1:95143518-95143529 |
11 | RCOR1 | chr1:95143232-95143536 | K562 | blood: | n/a | n/a |
12 | BHLHE40 | chr1:95143320-95143564 | K562 | blood: | n/a | n/a |
13 | USF1 | chr1:95143232-95143732 | K562 | blood: | n/a | n/a |
14 | USF1 | chr1:95143269-95143684 | HCT-116 | colon: | n/a | n/a |
15 | USF1 | chr1:95143250-95143609 | K562 | blood: | n/a | n/a |
16 | USF2 | chr1:95143363-95143638 | H1-hESC | embryonic stem cell: | n/a | chr1:95143518-95143529 |
17 | USF1 | chr1:95143279-95143641 | H1-hESC | embryonic stem cell: | n/a | n/a |
18 | USF1 | chr1:95143328-95143690 | A549 | lung: | n/a | n/a |
19 | USF1 | chr1:95143263-95143727 | H1-hESC | embryonic stem cell: | n/a | n/a |
20 | USF1 | chr1:95143265-95143670 | ECC-1 | luminal epithelium: | n/a | n/a |
21 | NFYB | chr1:95143252-95143686 | K562 | blood: | n/a | chr1:95143464-95143479 |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr1:95135759..95138517-chr1:95142176..95146453,3 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
PGBD4P7 | TF binding region |
rs_ID | r2[population] |
---|---|
rs10127519 | 0.90[YRI][hapmap] |
rs10127958 | 0.90[YRI][hapmap] |
rs10218699 | 0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs10218700 | 0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs10218701 | 0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs10493877 | 0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs10782990 | 0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs10782991 | 0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs10874879 | 0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs10874880 | 0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs10874881 | 0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs10874882 | 0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs10874883 | 0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs10874884 | 0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs11165192 | 0.90[YRI][hapmap] |
rs11165209 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11165211 | 1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11165212 | 0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs11165215 | 0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs11165217 | 0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs11165218 | 0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs11165219 | 0.80[AMR][1000 genomes] |
rs11165220 | 0.80[AMR][1000 genomes] |
rs11165221 | 0.80[AMR][1000 genomes] |
rs12085094 | 0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12089652 | 0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12116841 | 0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs12117807 | 0.83[AMR][1000 genomes] |
rs12120217 | 0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs12127717 | 0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs12128735 | 0.80[AMR][1000 genomes] |
rs12138432 | 0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12145601 | 0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs12409876 | 0.83[AMR][1000 genomes] |
rs12409905 | 0.83[AMR][1000 genomes] |
rs12409906 | 0.83[AMR][1000 genomes] |
rs12725936 | 0.92[AMR][1000 genomes];0.82[ASN][1000 genomes] |
rs12736683 | 0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs12739283 | 0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12739612 | 0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12739646 | 0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12740172 | 0.83[AMR][1000 genomes] |
rs12743410 | 0.92[AMR][1000 genomes];0.82[ASN][1000 genomes] |
rs12750395 | 0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs12756850 | 0.83[AMR][1000 genomes] |
rs12756853 | 0.83[AMR][1000 genomes] |
rs12757140 | 0.83[AMR][1000 genomes] |
rs12757198 | 0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12757945 | 0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs12758342 | 0.83[AMR][1000 genomes] |
rs12760023 | 0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12760228 | 0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12760666 | 0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1493275 | 0.80[AMR][1000 genomes] |
rs1493276 | 0.80[AMR][1000 genomes] |
rs1493277 | 0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs1772893 | 0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs1778190 | 0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs1873878 | 0.80[AMR][1000 genomes] |
rs1891871 | 0.80[AMR][1000 genomes] |
rs1994850 | 0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs2040074 | 0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs2040075 | 0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs2040076 | 0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs2040077 | 0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs2391384 | 0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs2391385 | 1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.96[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs2391387 | 0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs2893273 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs3956597 | 0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4000655 | 0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4000656 | 0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4000657 | 0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs4000658 | 1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs4240958 | 0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4240959 | 0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4240960 | 1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs4274076 | 0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4319342 | 0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4338361 | 0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4394665 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4567290 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4598496 | 0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4847329 | 0.95[YRI][hapmap] |
rs4847334 | 0.90[YRI][hapmap] |
rs4847337 | 1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs4847338 | 0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4847339 | 0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4847340 | 0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs4847341 | 0.80[AMR][1000 genomes] |
rs4847342 | 0.80[AMR][1000 genomes] |
rs4847343 | 0.80[AMR][1000 genomes] |
rs4847344 | 0.80[AMR][1000 genomes] |
rs4847345 | 0.80[AMR][1000 genomes] |
rs61773231 | 0.82[AMR][1000 genomes];0.86[ASN][1000 genomes] |
rs6663811 | 0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs7412205 | 0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7416454 | 0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7546594 | 0.81[AMR][1000 genomes] |
rs7546688 | 0.80[AMR][1000 genomes] |
rs841340 | 1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs841359 | 0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs841361 | 0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs841362 | 0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs841366 | 0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs859337 | 0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs923815 | 0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs964213 | 0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1001587 | chr1:95027691-95318680 | Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 18 gene(s) | inside rSNPs | diseases |
2 | esv2755232 | chr1:95119790-95151813 | Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
3 | nsv432509 | chr1:95119790-95151813 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
4 | esv2756851 | chr1:95119790-95158603 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
5 | esv2758950 | chr1:95119790-95158603 | Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
6 | nsv437227 | chr1:95122565-95143548 | Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
7 | nsv1001602 | chr1:95125965-95153262 | Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
8 | nsv1002928 | chr1:95126536-95152838 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
9 | nsv998738 | chr1:95126536-95155399 | Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
10 | nsv546853 | chr1:95127463-95154279 | Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
11 | nsv517330 | chr1:95128546-95153262 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
12 | nsv871001 | chr1:95128546-95171891 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
13 | nsv436535 | chr1:95128791-95155240 | Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
14 | nsv1001354 | chr1:95130666-95151813 | Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
15 | nsv1000399 | chr1:95130666-95152608 | Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
16 | nsv1009765 | chr1:95130666-95152838 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
17 | nsv1003354 | chr1:95130666-95153262 | Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
18 | nsv1013700 | chr1:95130666-95155387 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
19 | nsv1013561 | chr1:95130666-95155399 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
20 | nsv1012925 | chr1:95130666-95155534 | Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
21 | nsv999580 | chr1:95130666-95155585 | Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
22 | esv2421913 | chr1:95130678-95154279 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
23 | esv2764194 | chr1:95130678-95155597 | Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
24 | nsv1010621 | chr1:95130685-95152838 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
25 | nsv1004540 | chr1:95130685-95153262 | Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
26 | nsv1009168 | chr1:95130754-95152838 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
27 | nsv1007625 | chr1:95130754-95153262 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
28 | nsv1002560 | chr1:95130754-95155387 | Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
29 | nsv1013295 | chr1:95130754-95155399 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
30 | nsv442927 | chr1:95130766-95155399 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
31 | nsv1011128 | chr1:95130788-95155399 | Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
32 | nsv1014173 | chr1:95130795-95153262 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
33 | nsv1013150 | chr1:95131506-95152807 | Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
34 | nsv997636 | chr1:95131506-95152838 | Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
35 | nsv1004829 | chr1:95131506-95153262 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
36 | nsv1000486 | chr1:95131596-95155399 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
37 | nsv462539 | chr1:95131929-95151743 | Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
38 | nsv546854 | chr1:95131929-95151743 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
39 | nsv470726 | chr1:95131929-95153262 | Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
40 | nsv546855 | chr1:95131929-95153262 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
41 | nsv818267 | chr1:95131929-95153262 | Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
42 | esv3692780 | chr1:95131929-95154279 | Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
43 | nsv546856 | chr1:95131929-95154279 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
44 | nsv513993 | chr1:95132532-95154956 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
45 | esv34973 | chr1:95134179-95151813 | Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
46 | nsv546857 | chr1:95134182-95153262 | Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
47 | esv12694 | chr1:95134798-95156000 | Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
48 | nsv462550 | chr1:95136071-95154279 | Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
49 | nsv462561 | chr1:95136071-95154279 | Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
50 | nsv546858 | chr1:95136071-95154279 | Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:95126800-95164200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr1:95128400-95154600 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
3 | chr1:95135000-95154400 | Weak transcription | NHLF | lung |
4 | chr1:95135200-95144200 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
5 | chr1:95135400-95150400 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
6 | chr1:95138200-95148800 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
7 | chr1:95140000-95155600 | Weak transcription | HSMMtube | muscle |
8 | chr1:95140400-95151000 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
9 | chr1:95141000-95144400 | Genic enhancers | Fetal Intestine Small | intestine |
10 | chr1:95141000-95145200 | Enhancers | Stomach Mucosa | stomach |
11 | chr1:95141200-95143600 | Enhancers | Fetal Intestine Large | intestine |
12 | chr1:95141600-95143600 | Enhancers | Rectal Mucosa Donor 29 | rectum |
13 | chr1:95141600-95144200 | Enhancers | Rectal Mucosa Donor 31 | rectum |
14 | chr1:95141800-95144400 | Weak transcription | Gastric | stomach |
15 | chr1:95142200-95143400 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
16 | chr1:95142200-95144200 | Enhancers | Duodenum Mucosa | Duodenum |
17 | chr1:95142400-95143400 | Enhancers | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
18 | chr1:95142400-95143400 | Enhancers | HUES6 Cell Line | embryonic stem cell |
19 | chr1:95142600-95143400 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
20 | chr1:95142600-95143400 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
21 | chr1:95142600-95144000 | Weak transcription | Sigmoid Colon | Sigmoid Colon |
22 | chr1:95142800-95143400 | Enhancers | HUES64 Cell Line | embryonic stem cell |
23 | chr1:95142800-95148600 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
24 | chr1:95142800-95149400 | Weak transcription | Fetal Muscle Leg | muscle |
25 | chr1:95142800-95167800 | Weak transcription | Pancreas | Pancrea |
26 | chr1:95143000-95143400 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
27 | chr1:95143000-95151000 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
28 | chr1:95143200-95143400 | Enhancers | H1 Cell Line | embryonic stem cell |
29 | chr1:95143200-95143400 | Enhancers | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
30 | chr1:95143200-95143400 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
31 | chr1:95143200-95144000 | Enhancers | Primary neutrophils fromperipheralblood | blood |