Variant report

Variant	rs36097221
Chromosome Location	chr6:31847413-31847414
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:8)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:8 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:31846772-31847793	H1-hESC	embryonic stem cell:	n/a	n/a
2	POLR2A	chr6:31847136-31847495	K562	blood:	n/a	n/a
3	POLR2A	chr6:31846301-31847559	SK-N-MC	brain:	n/a	n/a
4	POLR2A	chr6:31847291-31847545	H1-hESC	embryonic stem cell:	n/a	n/a
5	POLR2A	chr6:31846985-31847641	HL-60	blood:	n/a	n/a
6	POLR2A	chr6:31846815-31847610	HepG2	liver:	n/a	n/a
7	POLR2A	chr6:31846800-31847767	PFSK-1	brain:	n/a	n/a
8	POLR2A	chr6:31847363-31847451	H1-hESC	embryonic stem cell:	n/a	n/a

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31844613..31847430-chr6:31865372..31868871,3	MCF-7	breast:
2	chr6:31837893..31841462-chr6:31843957..31848091,5	MCF-7	breast:
3	chr6:31846442..31848048-chr6:31868032..31869941,2	K562	blood:
4	chr6:31845609..31848674-chr6:31849036..31853301,8	K562	blood:
5	chr6:31847413..31850386-chr6:31864016..31867954,3	MCF-7	breast:
6	chr6:31802504..31804188-chr6:31847316..31849338,2	MCF-7	breast:
7	chr6:31845040..31847876-chr6:31859970..31863123,3	K562	blood:
8	chr6:31846387..31850562-chr6:31859687..31861704,3	MCF-7	breast:
9	chr6:31844767..31847605-chr6:31925658..31928567,2	MCF-7	breast:
10	chr6:31632488..31634160-chr6:31845506..31848503,2	MCF-7	breast:
11	chr6:31794807..31796884-chr6:31844966..31847954,2	MCF-7	breast:
12	chr6:31631416..31634262-chr6:31846927..31849993,4	K562	blood:
13	chr6:31846978..31851415-chr6:31853585..31859166,6	K562	blood:

No data

Variant related genes	Relation type
EHMT2-AS1	TF binding region
SLC44A4	TF binding region
ENSG00000204435	Chromatin interaction
ENSG00000204366	Chromatin interaction
ENSG00000237080	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000204356	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000204351	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs13192107	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13194698	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17201319	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs34287387	0.82[EUR][1000 genomes]
rs35092817	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35421785	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71563386	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71565312	1.00[ASN][1000 genomes]
rs73404147	0.82[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv601610	chr6:31280101-31960770	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	370 gene(s)	inside rSNPs	diseases
2	nsv601628	chr6:31280327-31990098	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
3	nsv601629	chr6:31280327-31996185	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
4	nsv601630	chr6:31280327-32011317	Genic enhancers Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
5	nsv601631	chr6:31280327-32017540	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
6	nsv1023939	chr6:31325961-32026747	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
7	nsv538188	chr6:31325961-32026747	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
8	nsv1021747	chr6:31386219-31907266	Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	330 gene(s)	inside rSNPs	diseases
9	nsv1033154	chr6:31550614-32009410	Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	326 gene(s)	inside rSNPs	diseases
10	nsv1017945	chr6:31609641-32481240	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
11	esv3428142	chr6:31615800-31881809	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	257 gene(s)	inside rSNPs	diseases
12	nsv884428	chr6:31728102-31870326	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
13	nsv462872	chr6:31778272-31864304	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
14	nsv601945	chr6:31778272-31864304	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
15	nsv601950	chr6:31785438-32492308	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
16	nsv601951	chr6:31785438-32496748	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
17	nsv601955	chr6:31785453-32484368	Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
18	nsv601956	chr6:31785453-32492308	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
19	nsv462874	chr6:31794592-31864304	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
20	nsv601959	chr6:31794592-31864304	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
21	nsv884472	chr6:31813898-31870856	Weak transcription Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
22	nsv508399	chr6:31829474-31902423	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
23	nsv884474	chr6:31836055-31870326	Genic enhancers Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
24	nsv462875	chr6:31838441-31907147	Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
25	nsv601960	chr6:31838441-31907147	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
26	nsv884475	chr6:31840625-31880320	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31832000-31856000	Weak transcription	Right Atrium	heart
2	chr6:31832400-31847600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr6:31832400-31847600	Weak transcription	NH-A	brain
4	chr6:31832400-31848200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr6:31832400-31850800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr6:31833200-31864200	Weak transcription	Fetal Heart	heart
7	chr6:31836400-31847600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:31836800-31847800	Weak transcription	Hela-S3	cervix
9	chr6:31839000-31849000	Weak transcription	HSMM	muscle
10	chr6:31839200-31848800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr6:31839400-31847600	Weak transcription	HMEC	breast
12	chr6:31839600-31847600	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr6:31842800-31848800	Weak transcription	Primary hematopoietic stem cells	blood
14	chr6:31843000-31847600	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr6:31843000-31848800	Weak transcription	K562	blood
16	chr6:31844400-31847600	Weak transcription	Liver	Liver
17	chr6:31845000-31848800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr6:31845200-31847600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr6:31845200-31847600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr6:31845200-31847600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr6:31845200-31847600	Weak transcription	Brain Cingulate Gyrus	brain
22	chr6:31845200-31847800	Weak transcription	NHDF-Ad	bronchial
23	chr6:31845400-31848600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr6:31845600-31847600	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr6:31845600-31847600	Weak transcription	Aorta	Aorta
26	chr6:31845600-31847600	Weak transcription	Brain Substantia Nigra	brain
27	chr6:31845600-31847600	Weak transcription	Ovary	ovary
28	chr6:31845600-31847600	Weak transcription	Dnd41	blood
29	chr6:31845600-31847800	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr6:31845600-31849200	Weak transcription	HUVEC	blood vessel
31	chr6:31845800-31847800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr6:31846200-31850000	Weak transcription	Psoas Muscle	Psoas
33	chr6:31846400-31847600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr6:31846400-31847800	Weak transcription	Fetal Lung	lung
35	chr6:31846400-31848200	Weak transcription	Primary B cells from cord blood	blood
36	chr6:31846400-31849000	Weak transcription	Fetal Brain Male	brain
37	chr6:31846600-31847600	Weak transcription	A549	lung
38	chr6:31846600-31847600	Weak transcription	HepG2	liver
39	chr6:31846800-31847800	Weak transcription	Rectal Smooth Muscle	rectum
40	chr6:31846800-31847800	Weak transcription	Small Intestine	intestine
41	chr6:31846800-31849000	Weak transcription	Fetal Kidney	kidney
42	chr6:31847000-31847600	Flanking Active TSS	Stomach Mucosa	stomach
43	chr6:31847000-31847800	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr6:31847000-31847800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
45	chr6:31847000-31850200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr6:31847000-31857800	Strong transcription	Osteobl	bone
47	chr6:31847000-31860800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr6:31847000-31863200	Strong transcription	Primary T helper cells fromperipheralblood	blood
49	chr6:31847000-31863600	Strong transcription	Fetal Brain Female	brain
50	chr6:31847000-31864000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links