Variant report

No data

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	1:151411623-151426875..1:151436817-151437878	Hela-S3	cervix:
2	1:151436817-151437878..1:151496437-151509688	Hela-S3	cervix:
3	chr1:151436059..151438699-chr1:151467400..151469749,2	MCF-7	breast:
4	1:151219411-151234038..1:151436817-151437878	Hela-S3	cervix:
5	1:151436817-151437878..1:151512437-151516085	GM12878	blood:
6	1:151180715-151199990..1:151436817-151437878	Hela-S3	cervix:
7	chr1:151436153..151438229-chr1:151463732..151466484,2	K562	blood:
8	chr1:151429172..151433890-chr1:151435781..151441025,8	MCF-7	breast:
9	1:151436817-151437878..1:151483211-151496437	Hela-S3	cervix:
10	1:151436817-151437878..1:151618750-151636526	GM12878	blood:
11	1:151270864-151283078..1:151436817-151437878	Hela-S3	cervix:
12	chr1:151436182..151439012-chr1:151480953..151482703,2	MCF-7	breast:
13	chr1:151431741..151434239-chr1:151435568..151437628,2	K562	blood:
14	1:151333184-151350267..1:151436817-151437878	Hela-S3	cervix:
15	1:151203965-151215310..1:151436817-151437878	Hela-S3	cervix:
16	1:151309061-151322694..1:151436817-151437878	Hela-S3	cervix:
17	1:151436817-151437878..1:151516085-151535167	GM12878	blood:
18	1:151254384-151268403..1:151436817-151437878	Hela-S3	cervix:
19	chr1:151437130..151438728-chr1:151510858..151512482,2	MCF-7	breast:
20	1:151427826-151434310..1:151436817-151437878	Hela-S3	cervix:
21	1:151368336-151375897..1:151436817-151437878	Hela-S3	cervix:
22	1:151436817-151437878..1:151478607-151483211	H1-hESC	embryonic stem cell:	embryo

No data

rSNPs within LD-proxies of this variant (count:8)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916272	chr1:150961809-151557253	Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	219 gene(s)	inside rSNPs	diseases
2	nsv831581	chr1:151289151-151478605	Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151431000-151445000	Weak transcription	Spleen	Spleen
2	chr1:151432400-151437800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:151432600-151445000	Weak transcription	Fetal Intestine Small	intestine
4	chr1:151432600-151445000	Weak transcription	Pancreas	Pancrea

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