Variant report

Variant	nsv558299
Chromosome Location	chr12:34081127-34252870
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1395)
CpG islands
(count:611)
Chromatin interactive
region (count:16)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1395 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:34098056-34098330	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:34174965-34175535	K562	blood:	n/a	chr12:34175026-34175042 chr12:34175027-34175043
3	ARID3A	chr12:34186930-34187207	HepG2	liver:	n/a	chr12:34187070-34187086 chr12:34187069-34187085
4	ARID3A	chr12:34186859-34187191	K562	blood:	n/a	chr12:34187070-34187086 chr12:34187069-34187085
5	ARID3A	chr12:34174917-34175527	HepG2	liver:	n/a	chr12:34175026-34175042 chr12:34175027-34175043
6	ATF1	chr12:34175112-34175525	K562	blood:	n/a	n/a
7	ATF1	chr12:34250260-34250470	K562	blood:	n/a	n/a
8	ATF2	chr12:34174909-34175573	GM12878	blood:	n/a	n/a
9	ATF2	chr12:34175155-34175514	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr12:34175036-34175597	GM12878	blood:	n/a	n/a
11	ATF2	chr12:34175128-34175510	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr12:34175051-34175608	A549	lung:	n/a	n/a
13	ATF3	chr12:34175027-34175625	A549	lung:	n/a	n/a
14	BACH1	chr12:34186566-34186928	K562	blood:	n/a	chr12:34186742-34186756
15	BACH1	chr12:34186563-34186928	H1-hESC	embryonic stem cell:	n/a	chr12:34186742-34186756
16	BATF	chr12:34207885-34208102	GM12878	blood:	n/a	n/a
17	BATF	chr12:34175171-34175544	GM12878	blood:	n/a	n/a
18	BATF	chr12:34207658-34207839	GM12878	blood:	n/a	n/a
19	BCL11A	chr12:34175171-34175530	GM12878	blood:	n/a	n/a
20	BCL3	chr12:34175028-34175635	A549	lung:	n/a	n/a
21	BCL3	chr12:34174944-34175580	A549	lung:	n/a	n/a
22	BCLAF1	chr12:34175019-34175599	K562	blood:	n/a	n/a
23	BCLAF1	chr12:34175028-34175613	K562	blood:	n/a	n/a
24	BCLAF1	chr12:34174957-34175674	GM12878	blood:	n/a	n/a
25	BCLAF1	chr12:34174911-34175619	GM12878	blood:	n/a	n/a
26	BHLHE40	chr12:34175068-34175500	GM12878	blood:	n/a	n/a
27	BHLHE40	chr12:34175238-34175547	K562	blood:	n/a	n/a
28	BHLHE40	chr12:34173962-34174140	K562	blood:	n/a	n/a
29	BHLHE40	chr12:34169331-34169611	K562	blood:	n/a	n/a
30	BRCA1	chr12:34175047-34175619	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr12:34175247-34175453	GM12878	blood:	n/a	n/a
32	CBX3	chr12:34174931-34175570	K562	blood:	n/a	n/a
33	CBX3	chr12:34174956-34175530	K562	blood:	n/a	n/a
34	CCNT2	chr12:34175341-34175565	K562	blood:	n/a	n/a
35	CEBPB	chr12:34154999-34155125	HepG2	liver:	n/a	chr12:34155080-34155091
36	CEBPB	chr12:34154999-34155122	K562	blood:	n/a	chr12:34155080-34155091
37	CEBPB	chr12:34175064-34175551	A549	lung:	n/a	n/a
38	CEBPB	chr12:34175151-34175418	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr12:34175132-34175376	HepG2	liver:	n/a	n/a
40	CEBPB	chr12:34134976-34135032	A549	lung:	n/a	n/a
41	CEBPB	chr12:34174895-34175630	GM12878	blood:	n/a	n/a
42	CEBPB	chr12:34231038-34231238	HepG2	liver:	n/a	chr12:34231113-34231124
43	CEBPB	chr12:34175140-34175561	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr12:34175063-34175487	IMR90	lung:	n/a	n/a
45	CEBPB	chr12:34195176-34195258	A549	lung:	n/a	n/a
46	CEBPB	chr12:34091487-34091752	MCF-7	breast:	n/a	n/a
47	CEBPB	chr12:34175063-34175463	K562	blood:	n/a	n/a
48	CEBPB	chr12:34175050-34175494	K562	blood:	n/a	n/a
49	CEBPB	chr12:34175182-34175403	MCF-7	breast:	n/a	n/a
50	CEBPB	chr12:34175041-34175483	A549	lung:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:34175262-34175312	SKMC	muscle:	n/a
2	chr12:34175262-34175312	SKMC	muscle:	n/a
3	chr12:34175126-34175176	ProgFib	skin:	n/a
4	chr12:34177660-34177710	NHBE	bronchial:	n/a
5	chr12:34175262-34175312	GM19239	blood:	n/a
6	chr12:34174976-34175026	AoSMC	blood vessel:	n/a
7	chr12:34175126-34175176	HCT-116	colon:	n/a
8	chr12:34175443-34175493	HCPEpiC	choroid plexus:	n/a
9	chr12:34175567-34175617	SKMC	muscle:	n/a
10	chr12:34181037-34181087	A549	lung:	n/a
11	chr12:34175262-34175312	MCF10A-Er-Src	breast:	n/a
12	chr12:34175262-34175312	Caco-2	colon:	n/a
13	chr12:34175262-34175312	SAEC	small airway:	n/a
14	chr12:34175445-34175495	CMK	blood:	n/a
15	chr12:34175567-34175617	NHBE	bronchial:	n/a
16	chr12:34175126-34175176	HCM	heart:	n/a
17	chr12:34175126-34175176	GM06990	blood:	n/a
18	chr12:34175445-34175495	ovcar-3	ovarian:	n/a
19	chr12:34177660-34177710	AG10803	skin:	n/a
20	chr12:34177660-34177710	MCF10A-Er-Src	breast:	n/a
21	chr12:34181037-34181087	AG09309	skin:	n/a
22	chr12:34175262-34175312	GM06990	blood:	n/a
23	chr12:34175454-34175504	HUVEC	blood vessel:	n/a
24	chr12:34175262-34175312	HNPCEpiC	eye:	n/a
25	chr12:34175454-34175504	Caco-2	colon:	n/a
26	chr12:34175445-34175495	HMEC	breast:	n/a
27	chr12:34175454-34175504	MCF10A-Er-Src	breast:	n/a
28	chr12:34175567-34175617	ProgFib	skin:	n/a
29	chr12:34177660-34177710	HAEpiC	amniotic membrane:	n/a
30	chr12:34175445-34175495	ProgFib	skin:	n/a
31	chr12:34175443-34175493	HAEpiC	amniotic membrane:	n/a
32	chr12:34175262-34175312	ovcar-3	ovarian:	n/a
33	chr12:34177660-34177710	SKMC	muscle:	n/a
34	chr12:34174976-34175026	ovcar-3	ovarian:	n/a
35	chr12:34175454-34175504	ProgFib	skin:	n/a
36	chr12:34175445-34175495	T-47D	breast:	n/a
37	chr12:34171667-34171717	GM12892	blood:	n/a
38	chr12:34175126-34175176	SK-N-SH	brain:	n/a
39	chr12:34181037-34181087	U87	brain:	n/a
40	chr12:34175445-34175495	HEEpiC	esophagus:	n/a
41	chr12:34175126-34175176	LNCaP	prostate:	n/a
42	chr12:34174976-34175026	GM06990	blood:	n/a
43	chr12:34171667-34171717	HCPEpiC	choroid plexus:	n/a
44	chr12:34175445-34175495	HCF	heart:	n/a
45	chr12:34174976-34175026	HMEC	breast:	n/a
46	chr12:34181037-34181087	HIPEpiC	eye:	n/a
47	chr12:34175445-34175495	Hela-S3	cervix:	n/a
48	chr12:34175262-34175312	Hepatocyte	liver:	n/a
49	chr12:34175443-34175493	NB4	blood:	n/a
50	chr12:34175443-34175493	GM12892	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:32907346..32909769-chr12:34153874..34155673,2	MCF-7	breast:
2	chr12:34098748..34102292-chr12:49653830..49659564,5	MCF-7	breast:
3	chr12:34241238..34243550-chr12:38853316..38855678,2	MCF-7	breast:
4	chr12:34159858..34162837-chr12:34175347..34177852,2	K562	blood:
5	chr12:32906662..32909285-chr12:34183695..34186206,2	K562	blood:
6	chr12:34175001..34175865-chr12:38710413..38711151,3	HCT-116	colon:
7	chr12:34145843..34147953-chr17:56709056..56711203,2	MCF-7	breast:
8	chr12:32905758..32908162-chr12:34183695..34185541,2	K562	blood:
9	chr12:32908405..32909605-chr12:34174701..34175708,3	MCF-7	breast:
10	chr12:34095993..34098950-chr12:34112537..34115292,2	MCF-7	breast:
11	chr12:34098184..34100062-chr12:60091369..60093533,4	MCF-7	breast:
12	chr12:34247375..34249864-chr12:34256794..34259523,2	MCF-7	breast:
13	chr12:34097991..34100054-chr12:60091596..60093323,2	MCF-7	breast:
14	chr12:33590585..33592422-chr12:34176176..34177683,2	MCF-7	breast:
15	chr12:34095993..34098950-chr12:34112537..34115292,2	MCF-7	breast:
16	chr12:34191233..34191868-chr12:34777963..34778741,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALG10-1	chr12:34190307-34190583	XLOC_009707
2	lnc-ALG10-1	chr12:34209496-34209704	XLOC_009707
3	lnc-ALG10-1	chr12:34208992-34209394	ENSG00000256538
4	lnc-ALG10-1	chr12:34208992-34209394	XLOC_009707
5	lnc-ALG10-1	chr12:34190373-34190583	ENSG00000256538
6	lnc-ALG10-1	chr12:34209496-34209675	ENSG00000256538

No data

Variant related genes	Relation type
ENSG00000201624	TF binding region
ENSG00000264446	TF binding region
ENSG00000245482	TF binding region
ENSG00000256538	TF binding region
RNU6-472P	TF binding region
ALG10	TF binding region
ENSG00000201624	CpG island
ENSG00000264446	CpG island
ENSG00000245482	CpG island
ENSG00000256538	CpG island
RNU6-472P	CpG island
ALG10	CpG island
ENSG00000139133	chromatin interactions
ENSG00000139131	chromatin interactions
ENSG00000258101	chromatin interactions
ENSG00000175548	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000167553	chromatin interactions
PPARGC1A	miRNA target sites

Extended variants
information (count: 3481 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:3481 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186701110	chr12:34090030-34090031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs547741568	chr12:34090031-34090032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191531073	chr12:34090032-34090033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs536403404	chr12:34090060-34090061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551875915	chr12:34090081-34090082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs569440372	chr12:34090094-34090095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549957932	chr12:34090097-34090098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs116375671	chr12:34090130-34090131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538738776	chr12:34090131-34090132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115687945	chr12:34090155-34090156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs142718180	chr12:34090222-34090223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs534110282	chr12:34090249-34090250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs147636394	chr12:34090308-34090309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573882265	chr12:34090320-34090321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542884528	chr12:34090335-34090336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183835895	chr12:34090341-34090342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs562658966	chr12:34090377-34090378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576233192	chr12:34090447-34090448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544751290	chr12:34090449-34090450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564913264	chr12:34090464-34090465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs111243606	chr12:34090474-34090475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548075359	chr12:34090532-34090533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186109388	chr12:34090583-34090584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190963150	chr12:34090593-34090594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537882467	chr12:34090663-34090664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs9669743	chr12:34090675-34090676	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs11835551	chr12:34090681-34090682	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs539145070	chr12:34090687-34090688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552355155	chr12:34090791-34090792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566072628	chr12:34090826-34090827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs182115619	chr12:34090843-34090844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534663756	chr12:34090845-34090846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs554993664	chr12:34090867-34090868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs574018520	chr12:34090874-34090875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536530893	chr12:34090877-34090878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556416129	chr12:34090891-34090892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs186586214	chr12:34090948-34090949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs552509082	chr12:34090949-34090950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs72208997	chr12:34090970-34090971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs10598450	chr12:34090972-34090973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs398055478	chr12:34090981-34090982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs571096067	chr12:34090990-34090991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs147761352	chr12:34091005-34091006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs372816022	chr12:34091012-34091013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs412066	chr12:34091025-34091026	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs140239007	chr12:34091046-34091047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs2636085	chr12:34091114-34091115	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs410847	chr12:34091126-34091127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs530353008	chr12:34091184-34091185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535901075	chr12:34091193-34091194	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chordoma	18071362	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:572 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:34090000-34090400	Enhancers	Liver	Liver
2	chr12:34090400-34090800	Weak transcription	Liver	Liver
3	chr12:34090800-34092000	Enhancers	Liver	Liver
4	chr12:34092000-34096800	Weak transcription	Liver	Liver
5	chr12:34093800-34130400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:34096800-34098000	Enhancers	HMEC	breast
7	chr12:34096800-34098200	Enhancers	Liver	Liver
8	chr12:34097800-34098200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr12:34097800-34098400	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr12:34098200-34098600	Flanking Active TSS	Liver	Liver
11	chr12:34098600-34098800	Enhancers	Liver	Liver
12	chr12:34099800-34100000	ZNF genes & repeats	Psoas Muscle	Psoas
13	chr12:34120200-34120800	Enhancers	HMEC	breast
14	chr12:34120400-34120800	Enhancers	NHEK	skin
15	chr12:34127800-34128000	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
16	chr12:34130400-34130800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr12:34130800-34141200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr12:34131200-34131800	Enhancers	Liver	Liver
19	chr12:34140600-34142000	Enhancers	HMEC	breast
20	chr12:34141000-34142400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr12:34141000-34142800	Enhancers	NHEK	skin
22	chr12:34141200-34142000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr12:34141400-34142000	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr12:34141800-34142600	Enhancers	HUVEC	blood vessel
25	chr12:34141800-34142800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr12:34142000-34142800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr12:34142000-34146800	Weak transcription	HMEC	breast
28	chr12:34142000-34147200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr12:34142400-34147400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr12:34142800-34143000	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr12:34142800-34147400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr12:34142800-34147400	Weak transcription	NHEK	skin
33	chr12:34143000-34149600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr12:34146800-34148400	Enhancers	HMEC	breast
35	chr12:34147200-34148800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr12:34147400-34148200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr12:34147400-34148400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr12:34147400-34148800	Enhancers	NHEK	skin
39	chr12:34147800-34148800	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr12:34148000-34148600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr12:34149400-34149800	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr12:34149400-34150600	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr12:34149600-34150600	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr12:34149800-34150200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr12:34150000-34150600	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr12:34150000-34150800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr12:34164000-34164200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr12:34169200-34169600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr12:34170200-34171000	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr12:34171000-34174200	Weak transcription	Monocytes-CD14+_RO01746	blood

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