Variant report

Variant	rs2756120
Chromosome Location	chr14:103990576-103990577
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	CTCF	chr14:103990480-103990661	Hela-S3	cervix:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
2	CTCF	chr14:103990460-103990610	GM12874	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
3	CTCF	chr14:103990480-103990630	GM12865	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
4	CTCF	chr14:103990545-103990601	GM12878	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
5	CTCF	chr14:103990517-103990633	A549	lung:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
6	CTCF	chr14:103990520-103990670	HMEC	breast:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
7	POLR2A	chr14:103989860-103990954	MCF10A-Er-Src	breast:	n/a	n/a
8	CTCF	chr14:103990486-103990673	MCF-7	breast:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
9	CTCF	chr14:103990540-103990690	GM12866	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
10	CTCF	chr14:103990500-103990650	Hela-S3	cervix:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
11	POLR2A	chr14:103990510-103991227	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr14:103990500-103990650	GM12868	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
13	CTCF	chr14:103990560-103990710	RPTEC	kidney:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
14	CTCF	chr14:103990526-103990621	GM19239	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
15	CTCF	chr14:103990461-103990723	H1-hESC	embryonic stem cell:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
16	CTCF	chr14:103990460-103990610	MCF-7	breast:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
17	CTCF	chr14:103990460-103990610	WERI-Rb-1	eye:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
18	CTCF	chr14:103990540-103990690	GM12864	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
19	CTCF	chr14:103990460-103990610	GM12878	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
20	JUND	chr14:103990391-103990691	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr14:103990420-103990690	MCF-7	breast:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
22	CTCF	chr14:103990520-103990670	GM12867	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
23	CTCF	chr14:103990560-103990710	GM12873	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
24	CTCF	chr14:103990445-103990635	HepG2	liver:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
25	CTCF	chr14:103990520-103990670	GM12869	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
26	CTCF	chr14:103990440-103990590	RPTEC	kidney:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
27	CTCF	chr14:103990501-103990664	NHEK	skin:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
28	CTCF	chr14:103990520-103990670	HepG2	liver:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
29	CTCF	chr14:103990560-103990624	GM12878	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
30	CTCF	chr14:103990520-103990630	MCF-7	breast:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
31	POLR2A	chr14:103990281-103990718	K562	blood:	n/a	n/a
32	CTCF	chr14:103990520-103990670	Caco-2	colon:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
33	CTCF	chr14:103990504-103990650	K562	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
34	CTCF	chr14:103990539-103990608	Gliobla	brain:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
35	CTCF	chr14:103990500-103990650	K562	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
36	CTCF	chr14:103990410-103990702	K562	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
37	CTCF	chr14:103990481-103990656	K562	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
38	CTCF	chr14:103990460-103990610	GM12872	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
39	CTCF	chr14:103990515-103990640	HepG2	liver:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
40	CTCF	chr14:103990480-103990630	GM12870	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
41	CTCF	chr14:103990540-103990603	GM10266	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
42	CTCF	chr14:103990440-103990590	HepG2	liver:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
43	CTCF	chr14:103990440-103990590	GM12864	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
44	CTCF	chr14:103990560-103990710	HRE	kidney:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
45	RAD21	chr14:103990300-103990744	H1-hESC	embryonic stem cell:	n/a	chr14:103990630-103990643
46	CTCF	chr14:103990460-103990610	GM12869	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
47	CTCF	chr14:103990480-103990630	GM12871	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
48	CTCF	chr14:103990400-103990653	H1-hESC	embryonic stem cell:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
49	CTCF	chr14:103990489-103990671	MCF-7	breast:	n/a	chr14:103990561-103990574 chr14:103990561-103990574
50	CTCF	chr14:103990460-103990610	HL-60	blood:	n/a	chr14:103990561-103990574 chr14:103990561-103990574

No.	Distal block	Cell Line	Cell type
1	chr14:103965151..103968057-chr14:103990191..103992747,2	MCF-7	breast:
2	chr14:103799200..103803060-chr14:103987408..103990865,9	K562	blood:
3	chr14:103989521..103992471-chr14:104020578..104022117,2	K562	blood:
4	chr14:103989795..103991937-chr14:104151715..104153875,2	K562	blood:
5	chr14:103989806..103992763-chr14:104031843..104033929,2	K562	blood:
6	chr14:103798500..103802639-chr14:103987592..103992121,9	K562	blood:

Variant related genes	Relation type
TRMT61A	TF binding region
CKB	TF binding region
ENSG00000100664	Chromatin interaction
ENSG00000126214	Chromatin interaction
ENSG00000201184	Chromatin interaction
ENSG00000075413	Chromatin interaction
ENSG00000259775	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs2756126	1.00[AFR][1000 genomes]
rs2765037	1.00[AFR][1000 genomes]
rs2765039	1.00[AFR][1000 genomes]
rs2765043	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs754288	0.85[AFR][1000 genomes]
rs941836	0.81[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:38 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534254	chr14:103470073-104023906	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	125 gene(s)	inside rSNPs	diseases
2	esv3332028	chr14:103581471-104328811	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers 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 target site	162 gene(s)	inside rSNPs	diseases
3	nsv832883	chr14:103927687-104120953	Genic enhancers Weak transcription Enhancers Strong transcription 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	63 gene(s)	inside rSNPs	diseases
4	nsv1044967	chr14:103954727-104007051	Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
5	esv1807091	chr14:103956182-104020454	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
6	esv1835824	chr14:103956182-104020454	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
7	nsv902297	chr14:103956182-104061646	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
8	nsv902298	chr14:103959289-104061646	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers 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 target site	43 gene(s)	inside rSNPs	diseases
9	nsv902299	chr14:103967504-104061646	Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
10	nsv902300	chr14:103967504-104205811	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
11	esv1834605	chr14:103969909-104003091	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers 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 target site	33 gene(s)	inside rSNPs	diseases
12	nsv902301	chr14:103979953-104003094	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
13	esv1850440	chr14:103979953-104007555	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
14	nsv902302	chr14:103979953-104018455	Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Strong transcription 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 target site	37 gene(s)	inside rSNPs	diseases
15	nsv902303	chr14:103979953-104034746	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription 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	42 gene(s)	inside rSNPs	diseases
16	nsv902304	chr14:103979953-104061646	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
17	nsv902305	chr14:103979953-104073551	Strong transcription Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
18	nsv827068	chr14:103982866-104021347	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
19	nsv902306	chr14:103984294-104003094	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
20	esv1835145	chr14:103984294-104014935	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
21	nsv902307	chr14:103986155-104003094	Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
22	esv1824096	chr14:103986255-103999371	Active TSS Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
23	esv1842368	chr14:103986255-103999371	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
24	esv1834274	chr14:103987140-103996205	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
25	esv1834291	chr14:103987140-103999371	Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
26	esv1839917	chr14:103987140-103999371	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
27	esv1845597	chr14:103987140-103999371	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
28	esv1851656	chr14:103987140-104007555	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
29	esv1839595	chr14:103987140-104034746	Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
30	esv1821012	chr14:103988059-103993060	Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
31	esv1809007	chr14:103988059-103999371	Enhancers Genic enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
32	esv1818214	chr14:103988059-103999371	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
33	esv1837939	chr14:103988059-103999371	Weak transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
34	esv1846909	chr14:103988059-103999371	Flanking Active TSS Active TSS Genic enhancers Enhancers Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
35	esv1794331	chr14:103988059-104004311	Weak transcription Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
36	nsv566020	chr14:103989279-103996396	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
37	nsv566021	chr14:103989639-104012982	Active TSS Enhancers Flanking Active TSS Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
38	esv1819920	chr14:103989971-104018096	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:103989400-103990800	Bivalent Enhancer	Stomach Mucosa	stomach
2	chr14:103989400-103993000	Enhancers	Fetal Lung	lung
3	chr14:103989400-103993600	Weak transcription	Gastric	stomach
4	chr14:103989600-103990600	Enhancers	HepG2	liver
5	chr14:103989600-103991000	Bivalent Enhancer	Fetal Muscle Leg	muscle
6	chr14:103989600-103991400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
7	chr14:103989600-103993400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr14:103989600-103994000	Weak transcription	Left Ventricle	heart
9	chr14:103989600-103994600	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr14:103989800-103990600	Weak transcription	K562	blood
11	chr14:103989800-103990800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr14:103989800-103990800	Enhancers	Brain Cingulate Gyrus	brain
13	chr14:103989800-103990800	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr14:103989800-103990800	Bivalent Enhancer	Fetal Stomach	stomach
15	chr14:103989800-103990800	Enhancers	Right Ventricle	heart
16	chr14:103989800-103991000	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr14:103989800-103991200	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr14:103989800-103991600	Enhancers	Colonic Mucosa	Colon
19	chr14:103989800-103991800	Weak transcription	Stomach Smooth Muscle	stomach
20	chr14:103989800-103992200	Enhancers	A549	lung
21	chr14:103989800-103992400	Weak transcription	Lung	lung
22	chr14:103989800-103992600	Weak transcription	Brain Hippocampus Middle	brain
23	chr14:103989800-103993000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr14:103989800-103993600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr14:103989800-103994000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr14:103989800-103994000	Weak transcription	Esophagus	oesophagus
27	chr14:103989800-103994000	Weak transcription	Ovary	ovary
28	chr14:103989800-103994000	Weak transcription	Right Atrium	heart
29	chr14:103989800-103994600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr14:103990000-103990800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
31	chr14:103990000-103990800	Weak transcription	Brain Anterior Caudate	brain
32	chr14:103990000-103990800	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr14:103990000-103991000	Weak transcription	Liver	Liver
34	chr14:103990000-103991200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr14:103990000-103991800	Weak transcription	Fetal Heart	heart
36	chr14:103990000-103991800	Enhancers	Rectal Smooth Muscle	rectum
37	chr14:103990000-103992400	Enhancers	Fetal Intestine Small	intestine
38	chr14:103990000-103992800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr14:103990000-103994000	Weak transcription	Brain Angular Gyrus	brain
40	chr14:103990000-103994200	Enhancers	Fetal Intestine Large	intestine
41	chr14:103990200-103990600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr14:103990200-103990600	Weak transcription	Adipose Nuclei	Adipose
43	chr14:103990200-103990600	Weak transcription	Brain Substantia Nigra	brain
44	chr14:103990200-103990800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr14:103990200-103991200	Enhancers	Brain Germinal Matrix	brain
46	chr14:103990200-103992000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr14:103990200-103992400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr14:103990200-103992600	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr14:103990200-103992800	Enhancers	Colon Smooth Muscle	Colon
50	chr14:103990200-103993400	Weak transcription	Hela-S3	cervix

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links