Variant report
Variant | rs3888720 |
---|---|
Chromosome Location | chr6:29782813-29782814 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:32)
- CpG islands (count:0)
- Chromatin interactive region (count:8)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:32 , 50 per page) page:
1
No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | YY1 | chr6:29782698-29782826 | K562 | blood: | n/a | n/a |
2 | HEY1 | chr6:29782343-29783082 | K562 | blood: | n/a | n/a |
3 | POLR2A | chr6:29782439-29783136 | K562 | blood: | n/a | n/a |
4 | ZBTB7A | chr6:29782602-29782813 | K562 | blood: | n/a | n/a |
5 | GATA1 | chr6:29782685-29783366 | PBDE | blood: | n/a | n/a |
6 | EP300 | chr6:29782783-29783116 | GM12878 | blood: | n/a | n/a |
7 | TAL1 | chr6:29782077-29783289 | K562 | blood: | n/a | n/a |
8 | MYC | chr6:29782714-29783082 | K562 | blood: | n/a | n/a |
9 | ZBTB7A | chr6:29782527-29783168 | K562 | blood: | n/a | chr6:29783010-29783018 |
10 | BCLAF1 | chr6:29782595-29783110 | K562 | blood: | n/a | n/a |
11 | GTF2F1 | chr6:29782812-29783122 | K562 | blood: | n/a | n/a |
12 | GTF2B | chr6:29782763-29783117 | K562 | blood: | n/a | n/a |
13 | POLR2A | chr6:29782635-29783132 | K562 | blood: | n/a | n/a |
14 | PML | chr6:29782466-29783099 | K562 | blood: | n/a | n/a |
15 | PML | chr6:29782588-29783167 | K562 | blood: | n/a | n/a |
16 | TEAD4 | chr6:29782714-29783265 | K562 | blood: | n/a | n/a |
17 | CBX3 | chr6:29782203-29783230 | K562 | blood: | n/a | n/a |
18 | POLR2A | chr6:29782465-29783139 | K562 | blood: | n/a | n/a |
19 | POLR2A | chr6:29782424-29783143 | K562 | blood: | n/a | n/a |
20 | HEY1 | chr6:29782550-29783054 | K562 | blood: | n/a | n/a |
21 | TEAD4 | chr6:29782577-29783272 | K562 | blood: | n/a | n/a |
22 | E2F6 | chr6:29782684-29782854 | K562 | blood: | n/a | n/a |
23 | TBP | chr6:29782765-29783192 | K562 | blood: | n/a | n/a |
24 | ZMIZ1 | chr6:29782692-29783111 | K562 | blood: | n/a | n/a |
25 | POLR2A | chr6:29782543-29783056 | K562 | blood: | n/a | n/a |
26 | USF1 | chr6:29782717-29783101 | K562 | blood: | n/a | n/a |
27 | BCLAF1 | chr6:29782754-29783154 | K562 | blood: | n/a | n/a |
28 | TAF7 | chr6:29782637-29783108 | K562 | blood: | n/a | n/a |
29 | TAF7 | chr6:29782726-29782971 | K562 | blood: | n/a | n/a |
30 | POLR2A | chr6:29782416-29783123 | K562 | blood: | n/a | n/a |
31 | RAD21 | chr6:29782513-29782830 | H1-hESC | embryonic stem cell: | n/a | chr6:29782780-29782793 |
32 | MAX | chr6:29782582-29783086 | K562 | blood: | n/a | n/a |
No data |
(count:8 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr6:29762168..29764765-chr6:29782319..29784097,2 | K562 | blood: | |
2 | chr6:29691597..29693774-chr6:29780569..29783300,2 | MCF-7 | breast: | |
3 | chr6:29778199..29781037-chr6:29781139..29783059,2 | K562 | blood: | |
4 | chr6:29721629..29723965-chr6:29782354..29784325,2 | K562 | blood: | |
5 | chr6:29776748..29779241-chr6:29782006..29784779,2 | K562 | blood: | |
6 | chr6:29780662..29785245-chr6:29788028..29791562,7 | K562 | blood: | |
7 | chr6:29712194..29714049-chr6:29781280..29783856,2 | K562 | blood: | |
8 | chr6:29755654..29758226-chr6:29780556..29783054,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
MICG | TF binding region |
ENSG00000204642 | Chromatin interaction |
ENSG00000225864 | Chromatin interaction |
ENSG00000237042 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs11751848 | 0.81[AFR][1000 genomes] |
rs11753296 | 0.84[ASN][1000 genomes] |
rs11753629 | 0.91[ASN][1000 genomes] |
rs11753654 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs11757126 | 0.81[AFR][1000 genomes] |
rs11757182 | 0.81[AFR][1000 genomes] |
rs12661041 | 0.83[ASN][1000 genomes] |
rs12661061 | 0.83[ASN][1000 genomes] |
rs12661066 | 0.83[ASN][1000 genomes] |
rs12662618 | 0.84[ASN][1000 genomes] |
rs1632969 | 0.86[ASN][1000 genomes] |
rs16896051 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs17178826 | 0.81[AFR][1000 genomes] |
rs17178952 | 0.94[AFR][1000 genomes] |
rs17179115 | 0.84[ASN][1000 genomes] |
rs17179122 | 0.84[ASN][1000 genomes] |
rs17185244 | 0.81[AFR][1000 genomes] |
rs17185377 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17185412 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs17185545 | 0.84[ASN][1000 genomes] |
rs2394176 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs2394177 | 1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2394180 | 0.84[ASN][1000 genomes] |
rs2394183 | 0.84[EUR][1000 genomes] |
rs2394184 | 0.84[EUR][1000 genomes] |
rs2394696 | 0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs28457697 | 0.84[EUR][1000 genomes] |
rs28552659 | 0.84[EUR][1000 genomes] |
rs28669293 | 0.84[EUR][1000 genomes] |
rs28728843 | 0.84[EUR][1000 genomes] |
rs28728869 | 0.84[EUR][1000 genomes] |
rs28743648 | 0.83[EUR][1000 genomes] |
rs28764567 | 0.83[EUR][1000 genomes] |
rs28764571 | 0.81[EUR][1000 genomes] |
rs28764613 | 0.84[EUR][1000 genomes] |
rs28764628 | 0.84[EUR][1000 genomes] |
rs28764750 | 0.84[EUR][1000 genomes] |
rs2894118 | 0.84[EUR][1000 genomes] |
rs34468824 | 1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34543080 | 0.92[AFR][1000 genomes] |
rs34833819 | 0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs35320382 | 0.97[AFR][1000 genomes] |
rs35494442 | 0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs3823321 | 0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs3882583 | 0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs3998745 | 0.83[AFR][1000 genomes] |
rs4098859 | 0.83[AFR][1000 genomes] |
rs55799039 | 0.84[EUR][1000 genomes] |
rs55868242 | 0.91[AFR][1000 genomes] |
rs56221809 | 0.96[AFR][1000 genomes] |
rs58795395 | 0.91[AFR][1000 genomes] |
rs59098250 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs59416725 | 0.88[AFR][1000 genomes] |
rs59457386 | 1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs59832006 | 0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs60299305 | 0.88[AFR][1000 genomes] |
rs60774155 | 1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61331935 | 1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs66472615 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs66776450 | 1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs67281546 | 0.85[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs6902658 | 0.83[EUR][1000 genomes] |
rs6922605 | 0.84[EUR][1000 genomes] |
rs72492263 | 0.81[AFR][1000 genomes] |
rs72492271 | 0.91[AFR][1000 genomes] |
rs72492273 | 0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs72492275 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72492276 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs72492277 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs72492278 | 0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs72492279 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72492280 | 0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72838212 | 0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72838213 | 1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72838218 | 0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72838286 | 0.84[ASN][1000 genomes] |
rs72838292 | 0.91[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs72838293 | 0.84[ASN][1000 genomes] |
rs72838299 | 0.84[ASN][1000 genomes] |
rs72838302 | 0.84[ASN][1000 genomes] |
rs72842103 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs72843669 | 0.83[EUR][1000 genomes] |
rs72843672 | 0.84[EUR][1000 genomes] |
rs72843675 | 0.84[EUR][1000 genomes] |
rs72843700 | 0.84[EUR][1000 genomes] |
rs72845903 | 0.84[EUR][1000 genomes] |
rs72845906 | 0.84[EUR][1000 genomes] |
rs72845913 | 0.81[EUR][1000 genomes] |
rs72846618 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72846685 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs72848310 | 1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73747715 | 0.84[EUR][1000 genomes] |
rs7742733 | 0.99[AFR][1000 genomes] |
rs7743372 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7743930 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7754512 | 0.83[ASN][1000 genomes] |
rs7755063 | 0.84[ASN][1000 genomes] |
rs7765903 | 0.84[ASN][1000 genomes] |
rs7769235 | 0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7769357 | 0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs7772553 | 0.83[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv20940 | chr6:29653954-29923410 | Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 46 gene(s) | inside rSNPs | diseases |
2 | nsv428139 | chr6:29659525-29892317 | Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 41 gene(s) | inside rSNPs | diseases |
3 | nsv427749 | chr6:29659525-29975144 | Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 53 gene(s) | inside rSNPs | diseases |
4 | nsv10809 | chr6:29692573-29794119 | Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 26 gene(s) | inside rSNPs | diseases |
5 | nsv883532 | chr6:29703262-29814963 | Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
6 | esv3441842 | chr6:29715749-29942950 | Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 47 gene(s) | inside rSNPs | diseases |
7 | esv11180 | chr6:29729381-29800066 | Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
8 | esv3332677 | chr6:29733187-29961463 | Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 43 gene(s) | inside rSNPs | diseases |
9 | esv3423001 | chr6:29733216-29878601 | Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 32 gene(s) | inside rSNPs | diseases |
10 | esv3475027 | chr6:29733297-29922699 | Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
11 | esv3475028 | chr6:29733297-29922699 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
12 | esv3420260 | chr6:29734457-29835593 | Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
13 | esv3330285 | chr6:29736281-29881328 | Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 31 gene(s) | inside rSNPs | diseases |
14 | esv3396224 | chr6:29754243-29888093 | Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 30 gene(s) | inside rSNPs | diseases |
15 | nsv965702 | chr6:29758408-29798943 | Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
16 | esv3430372 | chr6:29759523-29974277 | Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 42 gene(s) | inside rSNPs | diseases |
17 | esv3426050 | chr6:29761594-29918407 | Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 34 gene(s) | inside rSNPs | diseases |
18 | esv3431350 | chr6:29765473-29922767 | Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 34 gene(s) | inside rSNPs | diseases |
19 | nsv883540 | chr6:29772395-29784317 | Weak transcription Enhancers Bivalent Enhancer | TF binding regionChromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
20 | esv3354193 | chr6:29773857-29867902 | Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
21 | esv3451016 | chr6:29774115-29929436 | Strong transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 32 gene(s) | inside rSNPs | diseases |
22 | esv3369144 | chr6:29775824-29872385 | Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 26 gene(s) | inside rSNPs | diseases |
23 | esv3500392 | chr6:29777854-29871802 | Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
24 | esv3500393 | chr6:29777854-29871802 | Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
25 | esv3352548 | chr6:29777973-29783971 | Enhancers Bivalent Enhancer Weak transcription | TF binding regionChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
26 | esv3384912 | chr6:29778488-29872579 | ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
27 | esv3431922 | chr6:29779132-29873171 | Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
28 | esv3338581 | chr6:29780045-29890754 | Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 26 gene(s) | inside rSNPs | diseases |
29 | esv17468 | chr6:29782014-29923275 | Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 31 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:29779400-29783800 | Weak transcription | Right Atrium | heart |
2 | chr6:29781000-29783600 | Enhancers | K562 | blood |
3 | chr6:29782000-29783400 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
4 | chr6:29782000-29783600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
5 | chr6:29782000-29783800 | Weak transcription | NHEK | skin |
6 | chr6:29782600-29783000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
7 | chr6:29782800-29784000 | Weak transcription | HMEC | breast |