Variant report

Variant	rs35337578
Chromosome Location	chr6:31938451-31938452
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:60)
CpG islands
(count:0)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:60 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:31938168-31938523	H1-hESC	embryonic stem cell:	n/a	n/a
2	POLR2A	chr6:31937359-31938841	GM12878	blood:	n/a	n/a
3	POLR2A	chr6:31937284-31941234	K562	blood:	n/a	n/a
4	POLR2A	chr6:31937431-31941001	GM12892	blood:	n/a	n/a
5	POLR2A	chr6:31937473-31940648	PANC-1	pancreas:	n/a	n/a
6	POLR2A	chr6:31937360-31941122	HepG2	liver:	n/a	n/a
7	POLR2A	chr6:31935907-31941545	HepG2	liver:	n/a	n/a
8	POLR2A	chr6:31936260-31941395	K562	blood:	n/a	n/a
9	POLR2A	chr6:31937353-31941181	K562	blood:	n/a	n/a
10	POLR2A	chr6:31938389-31940570	HCT-116	colon:	n/a	n/a
11	POLR2A	chr6:31938002-31941081	MCF10A-Er-Src	breast:	n/a	n/a
12	HEY1	chr6:31938260-31938608	K562	blood:	n/a	n/a
13	POLR2A	chr6:31935432-31941169	K562	blood:	n/a	n/a
14	POLR2A	chr6:31937171-31940595	HepG2	liver:	n/a	n/a
15	POLR2A	chr6:31938281-31938474	GM12878	blood:	n/a	n/a
16	POLR2A	chr6:31938225-31938613	U87	brain:	n/a	n/a
17	POLR2A	chr6:31937671-31939011	HepG2	liver:	n/a	n/a
18	POLR2A	chr6:31937309-31938657	K562	blood:	n/a	n/a
19	POLR2A	chr6:31937740-31940568	HL-60	blood:	n/a	n/a
20	POLR2A	chr6:31936682-31940672	PFSK-1	brain:	n/a	n/a
21	POLR2A	chr6:31936493-31941269	GM12892	blood:	n/a	n/a
22	POLR2A	chr6:31937608-31940714	HL-60	blood:	n/a	n/a
23	POLR2A	chr6:31937600-31941256	PBDE	blood:	n/a	n/a
24	POLR2A	chr6:31937408-31940545	PANC-1	pancreas:	n/a	n/a
25	POLR2A	chr6:31937811-31941100	GM12892	blood:	n/a	n/a
26	PBX3	chr6:31937847-31940400	SK-N-SH	brain:	n/a	n/a
27	POLR2A	chr6:31937686-31940604	SK-N-SH	brain:	n/a	n/a
28	POLR2A	chr6:31938372-31938779	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr6:31938317-31940432	SK-N-SH	brain:	n/a	n/a
30	POLR2A	chr6:31936820-31941128	GM12891	blood:	n/a	n/a
31	POLR2A	chr6:31937483-31941074	HepG2	liver:	n/a	n/a
32	POLR2A	chr6:31937838-31938958	HepG2	liver:	n/a	n/a
33	FOSL2	chr6:31938404-31940424	HepG2	liver:	n/a	n/a
34	POLR2A	chr6:31938321-31940630	GM18505	blood:	n/a	n/a
35	JUN	chr6:31936988-31938663	K562	blood:	n/a	chr6:31937561-31937569 chr6:31937561-31937569 chr6:31937559-31937571 chr6:31937561-31937568 chr6:31937560-31937570
36	POLR2A	chr6:31934246-31941332	GM12878	blood:	n/a	n/a
37	POLR2A	chr6:31937836-31940575	GM12878	blood:	n/a	n/a
38	POLR2A	chr6:31937717-31938515	GM12891	blood:	n/a	n/a
39	POLR2A	chr6:31937598-31940875	PFSK-1	brain:	n/a	n/a
40	POLR2A	chr6:31937721-31940649	GM12891	blood:	n/a	n/a
41	ZBTB7A	chr6:31938349-31938565	K562	blood:	n/a	n/a
42	POLR2A	chr6:31937489-31940892	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr6:31937180-31941267	GM12892	blood:	n/a	n/a
44	POLR2A	chr6:31937633-31941047	GM12878	blood:	n/a	n/a
45	POLR2A	chr6:31937669-31939012	GM12878	blood:	n/a	n/a
46	ZNF263	chr6:31937474-31939008	HEK293-T-REx	kidney:	n/a	n/a
47	MTA3	chr6:31938336-31941041	GM12878	blood:	n/a	n/a
48	POLR2A	chr6:31935314-31941127	SK-N-MC	brain:	n/a	n/a
49	POLR2A	chr6:31938309-31939029	HUVEC	blood vessel:	n/a	n/a
50	POLR2A	chr6:31937678-31940458	A549	lung:	n/a	n/a

No data

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31867614..31871926-chr6:31937988..31942087,9	K562	blood:
2	chr17:56708053..56710341-chr6:31937045..31938607,2	MCF-7	breast:
3	chr6:31864068..31872693-chr6:31934470..31941847,12	MCF-7	breast:
4	chr6:31619280..31620873-chr6:31935756..31938534,2	K562	blood:
5	chr6:31781426..31784987-chr6:31937458..31940746,3	K562	blood:
6	chr6:31705460..31708202-chr6:31937853..31939865,2	K562	blood:
7	chr6:31628509..31634075-chr6:31935054..31938547,6	K562	blood:
8	chr6:31887719..31889549-chr6:31938108..31940067,2	MCF-7	breast:
9	chr6:31937794..31943427-chr6:31944150..31949640,18	K562	blood:
10	chr6:31866210..31871385-chr6:31935988..31941288,8	K562	blood:
11	chr6:31863628..31867852-chr6:31937946..31941812,10	MCF-7	breast:
12	chr6:31631495..31634660-chr6:31935613..31943206,9	K562	blood:
13	chr6:31868706..31872478-chr6:31938286..31942065,5	MCF-7	breast:
14	chr6:31863236..31865768-chr6:31937517..31940391,2	K562	blood:
15	chr6:31937366..31939733-chr6:32937181..32939543,3	K562	blood:
16	chr6:31587332..31589434-chr6:31937953..31940828,2	K562	blood:
17	chr6:31794009..31796794-chr6:31937769..31941181,3	K562	blood:
18	chr6:31705740..31708202-chr6:31937563..31940759,3	K562	blood:
19	chr6:31701251..31705281-chr6:31936091..31940341,4	K562	blood:
20	chr6:31802366..31805115-chr6:31938170..31940148,2	K562	blood:

No data

Variant related genes	Relation type
STK19	TF binding region
ENSG00000204435	Chromatin interaction
ENSG00000204410	Chromatin interaction
ENSG00000204344	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000201207	Chromatin interaction
ENSG00000223837	Chromatin interaction
ENSG00000201754	Chromatin interaction
ENSG00000255152	Chromatin interaction
ENSG00000204439	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000204256	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000204469	Chromatin interaction
ENSG00000213719	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000204366	Chromatin interaction
ENSG00000204390	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs12196385	0.82[ASN][1000 genomes]
rs12198173	0.82[ASN][1000 genomes]
rs12211410	0.82[ASN][1000 genomes]
rs13199524	0.82[ASN][1000 genomes]
rs17207867	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs204884	0.82[ASN][1000 genomes]
rs2077580	0.82[ASN][1000 genomes]
rs34241101	0.94[AFR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41315816	0.92[AMR][1000 genomes]
rs9267677	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:35 , 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	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
9	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
10	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
11	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
12	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
13	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
14	nsv601961	chr6:31868322-32484368	Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS 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	126 gene(s)	inside rSNPs	diseases
15	nsv427751	chr6:31871512-32092843	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
16	nsv428141	chr6:31871512-32092843	Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
17	esv2758043	chr6:31871512-32209113	Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
18	esv2759415	chr6:31871512-32209113	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
19	nsv830628	chr6:31887554-31947600	Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	69 gene(s)	inside rSNPs	diseases
20	nsv933250	chr6:31905060-32008005	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS 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	76 gene(s)	inside rSNPs	diseases
21	nsv934279	chr6:31905060-32013902	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
22	nsv884513	chr6:31922575-32066025	Bivalent Enhancer Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
23	nsv884514	chr6:31923052-31958960	Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Weak transcription Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
24	nsv932869	chr6:31924496-32013902	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
25	nsv933913	chr6:31924682-32009282	Active TSS Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
26	nsv284	chr6:31925739-31996721	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
27	nsv5247	chr6:31925739-32023216	Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
28	nsv884515	chr6:31930805-31946614	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	51 gene(s)	inside rSNPs	diseases
29	nsv884516	chr6:31931673-31946614	Active TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	51 gene(s)	inside rSNPs	diseases
30	nsv884517	chr6:31931673-32057627	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
31	nsv538190	chr6:31932347-32037290	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
32	nsv884518	chr6:31933518-31946614	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	50 gene(s)	inside rSNPs	diseases
33	nsv884519	chr6:31937116-31947594	Enhancers Genic enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	49 gene(s)	inside rSNPs	diseases
34	nsv884520	chr6:31938291-31946614	Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	49 gene(s)	inside rSNPs	diseases
35	nsv601970	chr6:31938451-31948029	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	49 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31927400-31938800	Weak transcription	Right Atrium	heart
2	chr6:31927600-31939400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr6:31927800-31938600	Strong transcription	NHEK	skin
4	chr6:31928000-31938600	Strong transcription	Rectal Smooth Muscle	rectum
5	chr6:31928000-31938600	Strong transcription	Sigmoid Colon	Sigmoid Colon
6	chr6:31928000-31938800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr6:31929000-31938600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr6:31934000-31938600	Weak transcription	Psoas Muscle	Psoas
9	chr6:31934400-31939200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr6:31935200-31938600	Weak transcription	Fetal Heart	heart
11	chr6:31936000-31938600	Weak transcription	Stomach Mucosa	stomach
12	chr6:31936800-31938600	Transcr. at gene 5' and 3'	K562	blood
13	chr6:31936800-31938800	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr6:31936800-31939200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr6:31937200-31938600	Genic enhancers	Muscle Satellite Cultured Cells	--
16	chr6:31937200-31938800	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr6:31937200-31939200	Genic enhancers	Spleen	Spleen
18	chr6:31937400-31938600	Genic enhancers	Brain Inferior Temporal Lobe	brain
19	chr6:31937400-31938800	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr6:31937400-31939000	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr6:31937400-31939200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:31937600-31938600	Transcr. at gene 5' and 3'	Stomach Smooth Muscle	stomach
23	chr6:31937600-31938800	Genic enhancers	Right Ventricle	heart
24	chr6:31937600-31939000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr6:31937600-31939000	Transcr. at gene 5' and 3'	Brain Dorsolateral Prefrontal Cortex	brain
26	chr6:31937600-31939000	Genic enhancers	Duodenum Smooth Muscle	Duodenum
27	chr6:31937800-31938600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr6:31937800-31938600	Transcr. at gene 5' and 3'	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr6:31937800-31938600	Genic enhancers	Rectal Mucosa Donor 29	rectum
30	chr6:31937800-31938600	Transcr. at gene 5' and 3'	Dnd41	blood
31	chr6:31937800-31938800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr6:31937800-31938800	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
33	chr6:31937800-31938800	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr6:31937800-31938800	Genic enhancers	Fetal Thymus	thymus
35	chr6:31937800-31938800	Genic enhancers	Gastric	stomach
36	chr6:31937800-31939000	Genic enhancers	Cortex derived primary cultured neurospheres	brain
37	chr6:31937800-31939200	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr6:31937800-31939400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr6:31938000-31938600	Transcr. at gene 5' and 3'	Breast Myoepithelial Primary Cells	Breast
40	chr6:31938000-31938600	Genic enhancers	Primary T cells fromperipheralblood	blood
41	chr6:31938000-31938600	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr6:31938000-31938600	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr6:31938000-31938600	Genic enhancers	Adipose Nuclei	Adipose
44	chr6:31938000-31938600	Transcr. at gene 5' and 3'	Fetal Brain Female	brain
45	chr6:31938000-31938600	Transcr. at gene 5' and 3'	Pancreas	Pancrea
46	chr6:31938000-31938600	Weak transcription	HSMM	muscle
47	chr6:31938000-31938800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr6:31938000-31938800	Genic enhancers	Primary T helper cells PMA-I stimulated	--
49	chr6:31938000-31938800	Genic enhancers	Brain Anterior Caudate	brain
50	chr6:31938000-31938800	Genic enhancers	Fetal Stomach	stomach

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