Variant report

Variant	rs3212031
Chromosome Location	chr14:104179679-104179680
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:44)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:44 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr14:104177060-104179960	U87	brain:	n/a	n/a
2	POLR2A	chr14:104179418-104179704	U87	brain:	n/a	n/a
3	POLR2A	chr14:104179568-104180038	A549	lung:	n/a	n/a
4	POLR2A	chr14:104179298-104180378	GM12891	blood:	n/a	n/a
5	POLR2A	chr14:104178819-104180617	HEK293	kidney:	n/a	n/a
6	POLR2A	chr14:104178073-104180844	GM19193	blood:	n/a	n/a
7	POLR2A	chr14:104178798-104180599	H1-hESC	embryonic stem cell:	n/a	n/a
8	POLR2A	chr14:104177685-104180996	K562	blood:	n/a	n/a
9	POLR2A	chr14:104176765-104181219	SK-N-MC	brain:	n/a	n/a
10	POLR2A	chr14:104178008-104180304	H1-hESC	embryonic stem cell:	n/a	n/a
11	POLR2A	chr14:104178803-104180762	GM12891	blood:	n/a	n/a
12	POLR2A	chr14:104179676-104180445	HepG2	liver:	n/a	n/a
13	POLR2A	chr14:104179620-104180048	MCF-7	breast:	n/a	n/a
14	POLR2A	chr14:104179662-104180768	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr14:104179344-104180060	Hela-S3	cervix:	n/a	n/a
16	POLR2A	chr14:104179628-104180093	GM12878	blood:	n/a	n/a
17	POLR2A	chr14:104178166-104180750	GM12892	blood:	n/a	n/a
18	POLR2A	chr14:104179604-104179880	K562	blood:	n/a	n/a
19	POLR2A	chr14:104177166-104181233	K562	blood:	n/a	n/a
20	POLR2A	chr14:104178955-104182843	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr14:104177162-104180671	HepG2	liver:	n/a	n/a
22	POLR2A	chr14:104177060-104179833	U87	brain:	n/a	n/a
23	POLR2A	chr14:104178799-104180193	Hela-S3	cervix:	n/a	n/a
24	POLR2A	chr14:104179535-104180440	MCF10A-Er-Src	breast:	n/a	n/a
25	POLR2A	chr14:104178681-104180824	GM12891	blood:	n/a	n/a
26	POLR2A	chr14:104179594-104180807	K562	blood:	n/a	n/a
27	POLR2A	chr14:104179368-104179868	HUVEC	blood vessel:	n/a	n/a
28	POLR2A	chr14:104177943-104181042	HL-60	blood:	n/a	n/a
29	POLR2A	chr14:104179610-104180038	GM12878	blood:	n/a	n/a
30	POLR2A	chr14:104179458-104179704	U87	brain:	n/a	n/a
31	POLR2A	chr14:104179268-104181003	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr14:104178653-104180702	GM12878	blood:	n/a	n/a
33	POLR2A	chr14:104178723-104181015	Raji	blood:	n/a	n/a
34	POLR2A	chr14:104178969-104180730	A549	lung:	n/a	n/a
35	POLR2A	chr14:104178083-104180769	ECC-1	luminal epithelium:	n/a	n/a
36	POLR2A	chr14:104177336-104180928	GM12892	blood:	n/a	n/a
37	POLR2A	chr14:104179489-104180076	ProgFib	skin:	n/a	n/a
38	POLR2A	chr14:104177987-104180767	GM12878	blood:	n/a	n/a
39	POLR2A	chr14:104177645-104180774	GM12892	blood:	n/a	n/a
40	POLR2A	chr14:104179537-104180605	GM12878	blood:	n/a	n/a
41	POLR2A	chr14:104179655-104180579	HepG2	liver:	n/a	n/a
42	POLR2A	chr14:104179600-104180783	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr14:104177466-104180933	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr14:104177263-104180149	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:104179660-104179710	K562	blood:	n/a
2	chr14:104179660-104179710	HEEpiC	esophagus:	n/a
3	chr14:104179660-104179710	HRPEpiC	eye:	n/a
4	chr14:104179660-104179710	NHDF-neo	bronchial:	n/a
5	chr14:104179660-104179710	HPAEpiC	pulmonary alveolar:	n/a
6	chr14:104179660-104179710	PANC-1	pancreas:	n/a
7	chr14:104179660-104179710	HCPEpiC	choroid plexus:	n/a
8	chr14:104179660-104179710	ProgFib	skin:	n/a
9	chr14:104179660-104179710	Hela-S3	cervix:	n/a
10	chr14:104179660-104179710	H1-hESC	embryonic stem cell:	embryo
11	chr14:104179660-104179710	HNPCEpiC	eye:	n/a
12	chr14:104179660-104179710	HRE	kidney:	n/a
13	chr14:104179660-104179710	GM12878	blood:	n/a
14	chr14:104179660-104179710	AG10803	skin:	n/a
15	chr14:104179660-104179710	NB4	blood:	n/a
16	chr14:104179660-104179710	HUVEC	blood vessel:	n/a
17	chr14:104179660-104179710	NH-A	brain:	n/a
18	chr14:104179660-104179710	HCM	heart:	n/a
19	chr14:104179660-104179710	SAEC	small airway:	n/a
20	chr14:104179660-104179710	PrEC	prostate:	n/a
21	chr14:104179660-104179710	GM19239	blood:	n/a
22	chr14:104179660-104179710	AG09319	gingival:	n/a
23	chr14:104179660-104179710	HCT-116	colon:	n/a
24	chr14:104179660-104179710	AoSMC	blood vessel:	n/a
25	chr14:104179660-104179710	ovcar-3	ovarian:	n/a
26	chr14:104179660-104179710	CMK	blood:	n/a
27	chr14:104179660-104179710	Caco-2	colon:	n/a
28	chr14:104179660-104179710	U87	brain:	n/a
29	chr14:104179660-104179710	AG04450	lung:	fetal
30	chr14:104179660-104179710	GM12891	blood:	n/a
31	chr14:104179660-104179710	T-47D	breast:	n/a
32	chr14:104179660-104179710	SK-N-SH_RA	brain:	n/a
33	chr14:104179660-104179710	HIPEpiC	eye:	n/a
34	chr14:104179660-104179710	IMR90	lung:	fetal
35	chr14:104179660-104179710	HCF	heart:	n/a
36	chr14:104179660-104179710	AG04449	skin:	fetal
37	chr14:104179660-104179710	NHBE	bronchial:	n/a
38	chr14:104179660-104179710	Jurkat	blood:	n/a
39	chr14:104179660-104179710	HepG2	liver:	n/a
40	chr14:104179660-104179710	NT2-D1	testis:	n/a
41	chr14:104179660-104179710	HAEpiC	amniotic membrane:	n/a
42	chr14:104179660-104179710	A549	lung:	n/a
43	chr14:104179660-104179710	SK-N-MC	brain:	n/a
44	chr14:104179660-104179710	BE2_C	brain:	n/a
45	chr14:104179660-104179710	ECC-1	luminal epithelium:	n/a
46	chr14:104179660-104179710	HRCEpiC	kidney:	n/a
47	chr14:104179660-104179710	AG09309	skin:	n/a
48	chr14:104179660-104179710	BJ	skin:	n/a
49	chr14:104179660-104179710	SKMC	muscle:	n/a
50	chr14:104179660-104179710	LNCaP	prostate:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:104091773..104098220-chr14:104179036..104183968,10	MCF-7	breast:
2	chr14:104178608..104186342-chr14:104186894..104193138,16	K562	blood:
3	chr14:103987454..103990068-chr14:104178702..104181671,2	K562	blood:
4	chr14:104095098..104097162-chr14:104179460..104182190,3	K562	blood:
5	chr14:104027886..104033252-chr14:104178637..104183670,7	MCF-7	breast:

No data

Variant related genes	Relation type
XRCC3	TF binding region
ZFYVE21	TF binding region
ENSG00000269963	TF binding region
ZFYVE21	CpG island
ENSG00000269963	CpG island
XRCC3	CpG island
ENSG00000126214	Chromatin interaction
ENSG00000256053	Chromatin interaction
ENSG00000253096	Chromatin interaction
ENSG00000166170	Chromatin interaction
ENSG00000100711	Chromatin interaction
ENSG00000166165	Chromatin interaction

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs11848174	0.92[ASN][1000 genomes]
rs11849022	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs17101760	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs17101763	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs17101767	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2024668	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2274265	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs3212049	1.00[ASN][1000 genomes]
rs3212056	1.00[ASN][1000 genomes]
rs3212058	1.00[ASN][1000 genomes]
rs3212064	1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs3212071	1.00[ASN][1000 genomes]
rs3212078	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs3212086	1.00[ASN][1000 genomes]
rs3212106	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs3212112	1.00[ASN][1000 genomes]
rs3212117	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs3212121	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs3212133	0.92[ASN][1000 genomes]
rs34100926	1.00[ASN][1000 genomes]
rs35905888	0.92[ASN][1000 genomes]
rs3736911	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs3742362	0.92[ASN][1000 genomes]
rs3742368	0.85[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs3742460	0.84[ASN][1000 genomes]
rs3742461	0.85[ASN][1000 genomes]
rs3742464	1.00[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs3783406	0.92[ASN][1000 genomes]
rs55650682	1.00[ASN][1000 genomes]
rs55653926	1.00[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs55729369	1.00[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs55958706	1.00[ASN][1000 genomes]
rs56726433	0.92[ASN][1000 genomes]
rs58899741	0.92[ASN][1000 genomes]
rs58909811	0.92[ASN][1000 genomes]
rs72561466	0.86[ASN][1000 genomes]
rs74085289	0.92[ASN][1000 genomes]
rs74086597	0.92[ASN][1000 genomes]
rs74088714	0.92[ASN][1000 genomes]
rs8009618	0.85[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs8020907	0.85[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs8021384	0.92[ASN][1000 genomes]
rs9282879	1.00[ASN][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	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
2	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
3	nsv1052010	chr14:104061472-104216267	Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
4	nsv542201	chr14:104061472-104216267	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
5	nsv456435	chr14:104061646-104198251	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
6	nsv566023	chr14:104061646-104198251	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
7	nsv902308	chr14:104087209-104211180	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
8	nsv1041329	chr14:104097750-104196346	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
9	nsv542202	chr14:104097750-104196346	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
10	nsv1048866	chr14:104100862-104195896	Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
11	nsv1045162	chr14:104140525-104594841	Flanking Active TSS Strong transcription Bivalent Enhancer Enhancers Active TSS Weak 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 lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
12	nsv542204	chr14:104140525-104594841	Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS 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 miRNA target site	87 gene(s)	inside rSNPs	diseases
13	nsv1041347	chr14:104141217-104186372	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
14	nsv902309	chr14:104143385-104198251	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
15	nsv902310	chr14:104143385-104205811	Genic enhancers Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
16	esv2758368	chr14:104147525-104412813	Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription 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 target site	56 gene(s)	inside rSNPs	diseases
17	esv2760013	chr14:104147525-104412813	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
18	nsv902311	chr14:104148339-104205811	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS 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	35 gene(s)	inside rSNPs	diseases
19	nsv902312	chr14:104155317-104211180	Strong transcription Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
20	esv1796914	chr14:104159882-104181369	Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
21	nsv527425	chr14:104162263-104198251	Transcr. at gene 5' and 3' Genic enhancers Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
22	nsv470673	chr14:104162263-104219949	Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
23	nsv902313	chr14:104162263-104378087	Bivalent Enhancer Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS 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	48 gene(s)	inside rSNPs	diseases
24	nsv902315	chr14:104165927-104190527	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
25	nsv902316	chr14:104173823-104195161	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
26	nsv902317	chr14:104175676-104194278	Active TSS Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104161200-104180000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr14:104161200-104180400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr14:104165400-104180400	Strong transcription	Thymus	Thymus
4	chr14:104169000-104180200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr14:104172600-104180600	Weak transcription	Primary B cells from cord blood	blood
6	chr14:104173000-104180400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr14:104174200-104179800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr14:104174200-104180000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr14:104174600-104180400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr14:104174800-104179800	Enhancers	Stomach Mucosa	stomach
11	chr14:104174800-104180400	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr14:104175000-104180600	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr14:104175200-104180000	Weak transcription	Primary B cells from peripheral blood	blood
14	chr14:104175200-104180600	Weak transcription	Fetal Lung	lung
15	chr14:104175200-104181000	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr14:104175600-104180400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr14:104175800-104180400	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr14:104175800-104180800	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr14:104176000-104180600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr14:104176200-104180400	Weak transcription	Fetal Brain Female	brain
21	chr14:104176400-104180200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr14:104176400-104180600	Weak transcription	Primary hematopoietic stem cells	blood
23	chr14:104176400-104180600	Weak transcription	Brain Angular Gyrus	brain
24	chr14:104176400-104180800	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr14:104176800-104180000	Weak transcription	Fetal Thymus	thymus
26	chr14:104177000-104180000	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr14:104177200-104180400	Genic enhancers	HUES6 Cell Line	embryonic stem cell
28	chr14:104177400-104179800	Enhancers	Adipose Nuclei	Adipose
29	chr14:104177400-104180400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr14:104177400-104180400	Enhancers	Gastric	stomach
31	chr14:104177400-104180600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr14:104177400-104180600	Genic enhancers	Fetal Muscle Trunk	muscle
33	chr14:104177400-104180800	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr14:104177600-104179800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr14:104177600-104179800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr14:104177600-104180000	Enhancers	Brain Substantia Nigra	brain
37	chr14:104177600-104180000	Weak transcription	Fetal Intestine Small	intestine
38	chr14:104177600-104180400	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr14:104177600-104180400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr14:104177600-104180600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr14:104177600-104180800	Enhancers	Right Ventricle	heart
42	chr14:104177600-104181200	Enhancers	Esophagus	oesophagus
43	chr14:104177800-104180000	Enhancers	Lung	lung
44	chr14:104177800-104180000	Enhancers	Spleen	Spleen
45	chr14:104177800-104180400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr14:104177800-104180400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr14:104177800-104180400	Enhancers	Left Ventricle	heart
48	chr14:104177800-104180600	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr14:104177800-104180600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr14:104177800-104180600	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links