Variant report

Variant	rs2802734
Chromosome Location	chr1:225063812-225063813
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

rs_ID	r²[population]
rs10399821	0.86[CHB][hapmap]
rs10399941	0.86[CHB][hapmap]
rs10915744	0.82[CHB][hapmap]
rs10915748	0.86[CHB][hapmap]
rs10915749	0.86[CHB][hapmap]
rs10915750	0.86[CHB][hapmap]
rs10915751	0.86[CHB][hapmap];0.91[CHD][hapmap]
rs10915757	0.86[CHB][hapmap];0.91[CHD][hapmap]
rs10915762	0.82[CHB][hapmap]
rs12068731	0.85[CHB][hapmap]
rs12071453	0.86[CHB][hapmap]
rs12073050	0.86[CHB][hapmap];0.91[CHD][hapmap]
rs12086122	0.86[CHB][hapmap]
rs12090624	0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12093545	0.91[CHD][hapmap]
rs1482278	0.82[CHB][hapmap]
rs1506071	0.86[LWK][hapmap];0.82[MKK][hapmap]
rs16858965	0.82[CHB][hapmap]
rs1892122	0.98[ASN][1000 genomes]
rs2244108	0.88[AFR][1000 genomes]
rs2244109	0.88[AFR][1000 genomes]
rs2244113	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2244198	0.88[AFR][1000 genomes]
rs2449301	0.82[AFR][1000 genomes]
rs2449305	0.85[AFR][1000 genomes]
rs2449306	0.85[AFR][1000 genomes]
rs2456344	0.85[AFR][1000 genomes]
rs2456350	0.85[AFR][1000 genomes]
rs2456354	0.85[AFR][1000 genomes]
rs2489327	0.86[LWK][hapmap];0.82[MKK][hapmap]
rs2489348	0.86[LWK][hapmap];0.82[MKK][hapmap]
rs2489352	0.86[LWK][hapmap];0.82[MKK][hapmap]
rs2501103	0.85[AFR][1000 genomes]
rs2501112	0.85[AFR][1000 genomes]
rs2662910	0.88[AFR][1000 genomes]
rs2662912	0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2662915	0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2802547	0.88[AFR][1000 genomes]
rs2802567	0.88[AFR][1000 genomes]
rs2802737	0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs3003126	0.84[AFR][1000 genomes]
rs4256778	0.88[AFR][1000 genomes]
rs6689287	0.86[CHB][hapmap]
rs6700281	0.86[CHB][hapmap]
rs7527885	0.86[CHB][hapmap]
rs981067	0.86[MKK][hapmap]

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:225060200-225064200	Enhancers	Fetal Intestine Small	intestine
2	chr1:225060800-225064000	Enhancers	Fetal Intestine Large	intestine
3	chr1:225061200-225067200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr1:225061200-225068800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr1:225061800-225067000	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr1:225062200-225066400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr1:225062600-225064000	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr1:225062800-225064000	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr1:225062800-225066800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr1:225063000-225064000	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr1:225063000-225064200	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr1:225063000-225066800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:225063000-225071600	Weak transcription	Ovary	ovary
14	chr1:225063200-225064000	Enhancers	H1 Cell Line	embryonic stem cell
15	chr1:225063200-225064000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr1:225063400-225064000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:225063400-225067200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr1:225063600-225067200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr1:225063600-225067200	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr1:225063600-225069800	Weak transcription	Liver	Liver
21	chr1:225063800-225064000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr1:225063800-225064000	Bivalent Enhancer	Fetal Kidney	kidney
23	chr1:225063800-225064000	Weak transcription	Pancreas	Pancrea
24	chr1:225063800-225067000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr1:225063800-225067200	Weak transcription	Fetal Lung	lung

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