Variant report

Variant	rs3803157
Chromosome Location	chr12:510602-510603
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:369)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr12:510337-511068	GM12891	blood:	n/a	n/a
2	SRF	chr12:510581-510856	HepG2	liver:	n/a	n/a
3	YY1	chr12:510443-511068	K562	blood:	n/a	chr12:510983-510994
4	NFIC	chr12:510432-510982	HepG2	liver:	n/a	n/a
5	POLR2A	chr12:510362-511168	GM19193	blood:	n/a	n/a
6	ZBTB33	chr12:510499-510826	HepG2	liver:	n/a	n/a
7	EGR1	chr12:510472-510856	K562	blood:	n/a	chr12:510678-510691 chr12:510626-510650
8	CEBPD	chr12:510388-511058	HepG2	liver:	n/a	n/a
9	MAX	chr12:510358-511659	A549	lung:	n/a	chr12:511240-511249 chr12:511240-511249 chr12:511238-511251 chr12:511239-511250
10	POLR2A	chr12:510369-511026	HepG2	liver:	n/a	n/a
11	POLR2A	chr12:510405-511080	U87	brain:	n/a	n/a
12	FOXP2	chr12:510517-510870	PFSK-1	brain:	n/a	n/a
13	RCOR1	chr12:510472-511044	HepG2	liver:	n/a	n/a
14	POLR2A	chr12:510416-510956	HepG2	liver:	n/a	n/a
15	ZBTB33	chr12:510555-510850	HCT-116	colon:	n/a	n/a
16	ELF1	chr12:510390-511025	MCF-7	breast:	n/a	n/a
17	FOS	chr12:510596-510834	MCF10A-Er-Src	breast:	n/a	chr12:510710-510719
18	MAX	chr12:510410-510992	K562	blood:	n/a	n/a
19	POLR2A	chr12:510402-511052	GM12878	blood:	n/a	n/a
20	POLR2A	chr12:510351-511080	U87	brain:	n/a	n/a
21	CREB1	chr12:510430-511031	ECC-1	luminal epithelium:	n/a	n/a
22	PML	chr12:510351-511107	K562	blood:	n/a	n/a
23	SP4	chr12:510526-511023	H1-hESC	embryonic stem cell:	n/a	chr12:510678-510694
24	NFIC	chr12:510408-510997	GM12878	blood:	n/a	n/a
25	SMC3	chr12:510424-511053	Hela-S3	cervix:	n/a	n/a
26	MAX	chr12:510254-511157	HepG2	liver:	n/a	n/a
27	ZBTB33	chr12:510444-510960	GM12878	blood:	n/a	n/a
28	CUX1	chr12:510320-510975	K562	blood:	n/a	n/a
29	CHD2	chr12:510448-511054	HepG2	liver:	n/a	n/a
30	BHLHE40	chr12:510198-511441	K562	blood:	n/a	n/a
31	NRF1	chr12:510431-511134	GM12878	blood:	n/a	n/a
32	MYC	chr12:510494-510915	MCF10A-Er-Src	breast:	n/a	n/a
33	SIN3AK20	chr12:510482-511073	SK-N-SH	brain:	n/a	n/a
34	MAX	chr12:510379-511578	Hela-S3	cervix:	n/a	chr12:511240-511249 chr12:511240-511249 chr12:511238-511251 chr12:511239-511250
35	YY1	chr12:510435-510918	HepG2	liver:	n/a	n/a
36	POLR2A	chr12:510319-511154	PFSK-1	brain:	n/a	n/a
37	POLR2A	chr12:510564-511030	K562	blood:	n/a	n/a
38	POLR2A	chr12:510560-511101	PANC-1	pancreas:	n/a	n/a
39	MYC	chr12:510356-511595	NB4	blood:	n/a	chr12:511240-511249 chr12:511240-511249 chr12:511238-511251 chr12:511239-511250
40	NFYB	chr12:510360-511010	Hela-S3	cervix:	n/a	chr12:510710-510725
41	E2F4	chr12:510424-511122	Hela-S3	cervix:	n/a	chr12:510683-510692
42	SIN3AK20	chr12:510581-511033	PANC-1	pancreas:	n/a	n/a
43	CEBPB	chr12:510317-510941	H1-hESC	embryonic stem cell:	n/a	chr12:510496-510509 chr12:510497-510508
44	ELF1	chr12:510359-510985	MCF-7	breast:	n/a	n/a
45	FOXM1	chr12:510230-511231	ECC-1	luminal epithelium:	n/a	n/a
46	TBP	chr12:510444-510996	GM12878	blood:	n/a	n/a
47	FOSL2	chr12:510244-511066	A549	lung:	n/a	chr12:510710-510719
48	POLR2A	chr12:510419-511032	MCF10A-Er-Src	breast:	n/a	n/a
49	STAT5A	chr12:510409-511202	GM12878	blood:	n/a	chr12:510499-510507
50	TBP	chr12:510262-511574	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:510594-510644	HepG2	liver:	n/a
2	chr12:510594-510644	Caco-2	colon:	n/a
3	chr12:510594-510644	HEEpiC	esophagus:	n/a
4	chr12:510594-510644	HCF	heart:	n/a
5	chr12:510594-510644	AG04449	skin:	fetal
6	chr12:510594-510644	LNCaP	prostate:	n/a
7	chr12:510594-510644	IMR90	lung:	fetal
8	chr12:510594-510644	RPTEC	kidney:	n/a
9	chr12:510594-510644	AG09309	skin:	n/a
10	chr12:510594-510644	SK-N-SH_RA	brain:	n/a
11	chr12:510594-510644	BJ	skin:	n/a
12	chr12:510594-510644	AG09319	gingival:	n/a
13	chr12:510594-510644	HPAEpiC	pulmonary alveolar:	n/a
14	chr12:510594-510644	SKMC	muscle:	n/a
15	chr12:510594-510644	AG04450	lung:	fetal
16	chr12:510594-510644	GM12891	blood:	n/a
17	chr12:510594-510644	ProgFib	skin:	n/a
18	chr12:510594-510644	HNPCEpiC	eye:	n/a
19	chr12:510594-510644	HL-60	blood:	n/a
20	chr12:510594-510644	BE2_C	brain:	n/a
21	chr12:510594-510644	Jurkat	blood:	n/a
22	chr12:510594-510644	HCT-116	colon:	n/a
23	chr12:510594-510644	NHDF-neo	bronchial:	n/a
24	chr12:510594-510644	HMEC	breast:	n/a
25	chr12:510594-510644	SK-N-MC	brain:	n/a
26	chr12:510594-510644	NT2-D1	testis:	n/a
27	chr12:510594-510644	NB4	blood:	n/a
28	chr12:510594-510644	PANC-1	pancreas:	n/a
29	chr12:510594-510644	SK-N-SH	brain:	n/a
30	chr12:510594-510644	SAEC	small airway:	n/a
31	chr12:510594-510644	GM19239	blood:	n/a
32	chr12:510594-510644	HRCEpiC	kidney:	n/a
33	chr12:510594-510644	HRPEpiC	eye:	n/a
34	chr12:510594-510644	CMK	blood:	n/a
35	chr12:510594-510644	Hepatocyte	liver:	n/a
36	chr12:510594-510644	Hela-S3	cervix:	n/a
37	chr12:510594-510644	PrEC	prostate:	n/a
38	chr12:510594-510644	HUVEC	blood vessel:	n/a
39	chr12:510594-510644	NHBE	bronchial:	n/a
40	chr12:510594-510644	GM12878	blood:	n/a
41	chr12:510594-510644	T-47D	breast:	n/a
42	chr12:510594-510644	PFSK-1	brain:	n/a
43	chr12:510594-510644	H1-hESC	embryonic stem cell:	embryo
44	chr12:510594-510644	MCF10A-Er-Src	breast:	n/a
45	chr12:510594-510644	NH-A	brain:	n/a
46	chr12:510594-510644	MCF-7	breast:	n/a
47	chr12:510594-510644	AoSMC	blood vessel:	n/a
48	chr12:510594-510644	ECC-1	luminal epithelium:	n/a
49	chr12:510594-510644	HCM	heart:	n/a
50	chr12:510594-510644	HCPEpiC	choroid plexus:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:497611..500419-chr12:508788..511712,2	MCF-7	breast:
2	chr12:508524..511172-chr12:751040..752702,2	MCF-7	breast:
3	chr12:496401..500895-chr12:509695..513736,6	K562	blood:
4	chr12:510462..511217-chr17:8113394..8114106,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
CCDC77	TF binding region
CCDC77	CpG island
ENSG00000178999	Chromatin interaction
ENSG00000073614	Chromatin interaction
ENSG00000177406	Chromatin interaction
ENSG00000120647	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs12578467	0.89[ASN][1000 genomes]
rs12582581	1.00[ASN][1000 genomes]
rs12582874	1.00[ASN][1000 genomes]
rs58735011	1.00[ASN][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	nsv1051726	chr12:282465-511843	Bivalent/Poised TSS Strong transcription Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv541304	chr12:282465-635505	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
3	nsv1042991	chr12:282465-666255	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	nsv1041574	chr12:282465-812000	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
5	nsv541305	chr12:282465-1016828	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
6	nsv869390	chr12:282465-1045994	Strong transcription Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
7	nsv1049944	chr12:282465-1232077	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer 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 miRNA target site	80 gene(s)	inside rSNPs	diseases
8	nsv541306	chr12:282465-1232077	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
9	nsv1050781	chr12:321353-783899	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
10	nsv1040849	chr12:321619-771493	Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
11	nsv541322	chr12:321619-771493	ZNF genes & repeats Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
12	nsv1035679	chr12:321619-781558	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
13	nsv1053519	chr12:321619-828175	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
14	nsv1044433	chr12:321619-1065402	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
15	nsv541323	chr12:321619-1065402	Strong transcription Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
16	esv2757484	chr12:335010-543206	Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Enhancers Active TSS Genic enhancers 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	18 gene(s)	inside rSNPs	diseases
17	esv2759875	chr12:335010-990544	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
18	nsv1045638	chr12:349031-893536	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
19	nsv541325	chr12:349031-893536	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
20	nsv1050646	chr12:362398-658665	Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
21	nsv541326	chr12:362398-658665	Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
22	nsv949469	chr12:380411-1122450	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
23	nsv898565	chr12:428131-564185	Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
24	nsv1052201	chr12:429128-515675	Weak transcription Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
25	nsv541328	chr12:429128-515675	Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
26	nsv442250	chr12:432808-543847	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
27	esv2756520	chr12:433151-543206	Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
28	nsv1050226	chr12:441032-743195	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
29	nsv1035222	chr12:449993-515675	Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
30	esv2758290	chr12:457433-990544	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
31	nsv949226	chr12:493900-814882	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
32	nsv898566	chr12:499041-570917	Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
33	nsv1036822	chr12:504573-586674	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
34	nsv541329	chr12:504573-586674	Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
35	nsv514668	chr12:506474-521532	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr12:509400-511800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr12:510000-510800	Enhancers	Spleen	Spleen
3	chr12:510000-511200	Active TSS	Stomach Smooth Muscle	stomach
4	chr12:510000-511400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr12:510000-511400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
6	chr12:510000-511400	Active TSS	Brain Germinal Matrix	brain
7	chr12:510000-511400	Active TSS	Psoas Muscle	Psoas
8	chr12:510000-511600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr12:510000-511600	Active TSS	Fetal Intestine Small	intestine
10	chr12:510000-511800	Active TSS	iPS-15b Cell Line	embryonic stem cell
11	chr12:510000-511800	Active TSS	iPS-18 Cell Line	embryonic stem cell
12	chr12:510000-511800	Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr12:510000-511800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr12:510000-512000	Active TSS	H1 Cell Line	embryonic stem cell
15	chr12:510000-512000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr12:510000-512000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr12:510000-512000	Active TSS	HUES64 Cell Line	embryonic stem cell
18	chr12:510000-512000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr12:510000-512200	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr12:510000-512200	Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr12:510000-512200	Active TSS	HUES6 Cell Line	embryonic stem cell
22	chr12:510200-511000	Active TSS	Rectal Mucosa Donor 29	rectum
23	chr12:510200-511200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr12:510200-511200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
25	chr12:510200-511200	Active TSS	Brain Cingulate Gyrus	brain
26	chr12:510200-511200	Active TSS	Brain Inferior Temporal Lobe	brain
27	chr12:510200-511400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr12:510200-511400	Active TSS	Aorta	Aorta
29	chr12:510200-511400	Active TSS	Fetal Intestine Large	intestine
30	chr12:510200-511400	Active TSS	Fetal Kidney	kidney
31	chr12:510200-511400	Active TSS	Fetal Stomach	stomach
32	chr12:510200-511400	Active TSS	Left Ventricle	heart
33	chr12:510200-511400	Active TSS	Right Ventricle	heart
34	chr12:510200-511400	Active TSS	Thymus	Thymus
35	chr12:510200-511600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
36	chr12:510200-511600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr12:510200-511600	Active TSS	Fetal Brain Female	brain
38	chr12:510200-511600	Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr12:510200-511600	Active TSS	Right Atrium	heart
40	chr12:510200-511600	Active TSS	HSMM	muscle
41	chr12:510200-511600	Active TSS	HSMMtube	muscle
42	chr12:510200-511600	Active TSS	K562	blood
43	chr12:510200-511600	Active TSS	NHDF-Ad	bronchial
44	chr12:510200-511800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr12:510200-512000	Active TSS	H9 Cell Line	embryonic stem cell
46	chr12:510200-512000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr12:510200-512000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
48	chr12:510200-512000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr12:510400-510800	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
50	chr12:510400-511000	Active TSS	Breast Myoepithelial Primary Cells	Breast

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