Variant report

Variant	rs144431937
Chromosome Location	chr6:29977071-29977072
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:29976463-29977224	GM12892	blood:	n/a	n/a
2	POLR2A	chr6:29976869-29977198	GM12878	blood:	n/a	n/a
3	POLR2A	chr6:29976358-29978082	GM12878	blood:	n/a	n/a
4	POLR2A	chr6:29976795-29977434	GM12891	blood:	n/a	n/a
5	POLR2A	chr6:29976382-29978083	GM12892	blood:	n/a	n/a
6	POLR2A	chr6:29976870-29977098	GM12891	blood:	n/a	n/a

Variant related genes	Relation type
HCG4P3	TF binding region

Extended variants
information (count: 10 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3391180	chr6:29798321-29977430	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv508398	chr6:29825777-30003403	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	esv2641340	chr6:29913287-29978544	Strong transcription Enhancers Bivalent/Poised TSS Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	esv3378806	chr6:29913464-29978179	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	esv3496792	chr6:29913818-29977071	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	esv3496793	chr6:29913818-29977071	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv1031115	chr6:29934199-30058223	Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
8	nsv538172	chr6:29934199-30058223	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
9	nsv601475	chr6:29963179-29977973	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
10	nsv981126	chr6:29976644-29978250	Weak transcription Strong transcription	TF binding region CpG island lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29974800-29981000	Weak transcription	Hela-S3	cervix
2	chr6:29974800-30002400	Weak transcription	Dnd41	blood
3	chr6:29975200-30027800	Weak transcription	Aorta	Aorta
4	chr6:29975400-29978800	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr6:29975400-29985200	Weak transcription	Lung	lung
6	chr6:29975600-29979200	Weak transcription	Ovary	ovary
7	chr6:29975600-29979200	Weak transcription	Pancreas	Pancrea
8	chr6:29975600-29985000	Weak transcription	Liver	Liver
9	chr6:29975600-29985200	Weak transcription	Primary B cells from cord blood	blood
10	chr6:29975600-29987200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr6:29975600-29987600	Weak transcription	HepG2	liver
12	chr6:29975600-30027800	Weak transcription	Right Ventricle	heart
13	chr6:29975800-29986600	Weak transcription	Esophagus	oesophagus
14	chr6:29975800-30027800	Weak transcription	Gastric	stomach
15	chr6:29976200-29986600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr6:29976200-29987800	Weak transcription	Primary B cells from peripheral blood	blood
17	chr6:29976200-30001800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr6:29976400-29977800	Strong transcription	Spleen	Spleen
19	chr6:29976600-29987000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr6:29976600-29987800	Weak transcription	Adipose Nuclei	Adipose
21	chr6:29976600-30023000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr6:29976800-29977200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr6:29976800-29978000	Strong transcription	Thymus	Thymus
24	chr6:29976800-29985800	Weak transcription	Left Ventricle	heart
25	chr6:29976800-29990000	Weak transcription	NHLF	lung
26	chr6:29976800-30000800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr6:29977000-29977400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
28	chr6:29977000-30002000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr6:29977000-30002000	Weak transcription	Primary T helper cells PMA-I stimulated	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links