Variant report

Variant	nsv980393
Chromosome Location	chr4:2927263-2930956
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:110)
CpG islands
(count:611)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:110 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr4:2927983-2928205	GM12878	blood:	n/a	n/a
2	CEBPB	chr4:2930443-2930776	ECC-1	luminal epithelium:	n/a	chr4:2930599-2930610
3	CEBPB	chr4:2930424-2930859	ECC-1	luminal epithelium:	n/a	chr4:2930599-2930610
4	CEBPB	chr4:2930489-2930737	HepG2	liver:	n/a	chr4:2930599-2930610
5	CEBPB	chr4:2930479-2930637	H1-hESC	embryonic stem cell:	n/a	chr4:2930599-2930610
6	CEBPB	chr4:2930510-2930710	K562	blood:	n/a	chr4:2930599-2930610
7	CEBPB	chr4:2930462-2930732	A549	lung:	n/a	chr4:2930599-2930610
8	CTCF	chr4:2930456-2930551	Hela-S3	cervix:	n/a	n/a
9	CTCF	chr4:2930340-2930490	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr4:2929140-2929290	WERI-Rb-1	eye:	n/a	n/a
11	MTA3	chr4:2930798-2931436	GM12878	blood:	n/a	n/a
12	NFATC1	chr4:2930450-2931002	GM12878	blood:	n/a	n/a
13	POLR2A	chr4:2930520-2930963	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr4:2930105-2936184	HL-60	blood:	n/a	n/a
15	POLR2A	chr4:2930935-2932115	GM12878	blood:	n/a	n/a
16	POLR2A	chr4:2929435-2929495	HUVEC	blood vessel:	n/a	n/a
17	POLR2A	chr4:2929301-2929325	GM12878	blood:	n/a	n/a
18	POLR2A	chr4:2930416-2932233	MCF10A-Er-Src	breast:	n/a	n/a
19	POLR2A	chr4:2930208-2931751	SK-N-MC	brain:	n/a	n/a
20	POLR2A	chr4:2930625-2931632	GM12891	blood:	n/a	n/a
21	POLR2A	chr4:2930548-2931277	SK-N-SH	brain:	n/a	n/a
22	POLR2A	chr4:2930292-2930588	HUVEC	blood vessel:	n/a	n/a
23	POLR2A	chr4:2930462-2930479	Hela-S3	cervix:	n/a	n/a
24	POLR2A	chr4:2929804-2929994	A549	lung:	n/a	n/a
25	POLR2A	chr4:2930118-2940539	K562	blood:	n/a	n/a
26	POLR2A	chr4:2930724-2930856	A549	lung:	n/a	n/a
27	POLR2A	chr4:2927918-2928235	HepG2	liver:	n/a	n/a
28	POLR2A	chr4:2930571-2934637	PFSK-1	brain:	n/a	n/a
29	POLR2A	chr4:2930044-2931429	U87	brain:	n/a	n/a
30	POLR2A	chr4:2930179-2933129	PFSK-1	brain:	n/a	n/a
31	POLR2A	chr4:2930507-2930517	MCF-7	breast:	n/a	n/a
32	POLR2A	chr4:2930202-2930900	MCF-7	breast:	n/a	n/a
33	POLR2A	chr4:2930497-2930863	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr4:2929025-2929238	HepG2	liver:	n/a	n/a
35	POLR2A	chr4:2930108-2936184	GM12878	blood:	n/a	n/a
36	POLR2A	chr4:2930152-2930943	ECC-1	luminal epithelium:	n/a	n/a
37	POLR2A	chr4:2930187-2932645	GM12892	blood:	n/a	n/a
38	POLR2A	chr4:2930022-2934363	GM12892	blood:	n/a	n/a
39	POLR2A	chr4:2930557-2930578	MCF-7	breast:	n/a	n/a
40	POLR2A	chr4:2930464-2931518	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr4:2930372-2930806	K562	blood:	n/a	n/a
42	POLR2A	chr4:2930261-2931104	GM12878	blood:	n/a	n/a
43	POLR2A	chr4:2929224-2929250	K562	blood:	n/a	n/a
44	POLR2A	chr4:2930159-2931718	GM12891	blood:	n/a	n/a
45	POLR2A	chr4:2930209-2930437	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr4:2929759-2929832	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr4:2929559-2936017	GM12878	blood:	n/a	n/a
48	POLR2A	chr4:2930410-2930710	H1-neurons	neurons:	n/a	n/a
49	POLR2A	chr4:2930254-2934156	A549	lung:	n/a	n/a
50	POLR2A	chr4:2930106-2930115	K562	blood:	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	chr4:2930203-2930253	GM19239	blood:	n/a
2	chr4:2930203-2930253	GM19239	blood:	n/a
3	chr4:2930306-2930356	NT2-D1	testis:	n/a
4	chr4:2928238-2928288	AG10803	skin:	n/a
5	chr4:2928238-2928288	HCM	heart:	n/a
6	chr4:2928060-2928110	PANC-1	pancreas:	n/a
7	chr4:2927882-2927932	BE2_C	brain:	n/a
8	chr4:2930306-2930356	HNPCEpiC	eye:	n/a
9	chr4:2928179-2928229	RPTEC	kidney:	n/a
10	chr4:2929622-2929672	GM19239	blood:	n/a
11	chr4:2930306-2930356	HCF	heart:	n/a
12	chr4:2930306-2930356	PANC-1	pancreas:	n/a
13	chr4:2927882-2927932	SK-N-MC	brain:	n/a
14	chr4:2929622-2929672	Jurkat	blood:	n/a
15	chr4:2928238-2928288	AoSMC	blood vessel:	n/a
16	chr4:2928179-2928229	HEK293	kidney:	embryo
17	chr4:2929622-2929672	HPAEpiC	pulmonary alveolar:	n/a
18	chr4:2928238-2928288	SKMC	muscle:	n/a
19	chr4:2928238-2928288	GM06990	blood:	n/a
20	chr4:2930306-2930356	GM12892	blood:	n/a
21	chr4:2930306-2930356	IMR90	lung:	fetal
22	chr4:2930306-2930356	SK-N-MC	brain:	n/a
23	chr4:2930073-2930123	GM06990	blood:	n/a
24	chr4:2927882-2927932	NHDF-neo	bronchial:	n/a
25	chr4:2928179-2928229	HCT-116	colon:	n/a
26	chr4:2929576-2929626	HUVEC	blood vessel:	n/a
27	chr4:2928238-2928288	HPAEpiC	pulmonary alveolar:	n/a
28	chr4:2928060-2928110	GM12892	blood:	n/a
29	chr4:2930306-2930356	PFSK-1	brain:	n/a
30	chr4:2928179-2928229	HUVEC	blood vessel:	n/a
31	chr4:2928179-2928229	SK-N-SH	brain:	n/a
32	chr4:2927882-2927932	AG04449	skin:	fetal
33	chr4:2930306-2930356	AG09319	gingival:	n/a
34	chr4:2928238-2928288	NHBE	bronchial:	n/a
35	chr4:2930306-2930356	PrEC	prostate:	n/a
36	chr4:2930203-2930253	HRPEpiC	eye:	n/a
37	chr4:2927882-2927932	HIPEpiC	eye:	n/a
38	chr4:2929576-2929626	HCM	heart:	n/a
39	chr4:2928060-2928110	PrEC	prostate:	n/a
40	chr4:2929622-2929672	HAEpiC	amniotic membrane:	n/a
41	chr4:2928179-2928229	H1-hESC	embryonic stem cell:	embryo
42	chr4:2928179-2928229	NH-A	brain:	n/a
43	chr4:2928179-2928229	GM12892	blood:	n/a
44	chr4:2929622-2929672	HRE	kidney:	n/a
45	chr4:2930361-2930411	GM19239	blood:	n/a
46	chr4:2930203-2930253	LNCaP	prostate:	n/a
47	chr4:2930361-2930411	HEEpiC	esophagus:	n/a
48	chr4:2928179-2928229	MCF10A-Er-Src	breast:	n/a
49	chr4:2929622-2929672	A549	lung:	n/a
50	chr4:2928060-2928110	GM12878	blood:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:2873606..2876373-chr4:2925507..2927684,2	MCF-7	breast:
2	chr4:2903718..2915473-chr4:2930612..2941584,27	MCF-7	breast:
3	chr4:2812607..2814330-chr4:2927336..2930211,2	MCF-7	breast:
4	chr4:2905536..2909706-chr4:2929255..2933631,5	MCF-7	breast:
5	chr4:2909857..2911472-chr4:2925477..2927647,2	K562	blood:
6	chr16:30389337..30390138-chr4:2930017..2930517,2	NB4	blood:
7	chr4:2798213..2801828-chr4:2930948..2933812,4	MCF-7	breast:
8	chr4:2844628..2846821-chr4:2925950..2928753,2	MCF-7	breast:
9	chr4:2819921..2821787-chr4:2928903..2930809,2	K562	blood:
10	chr4:2790052..2809152-chr4:2930639..2948075,83	MCF-7	breast:
11	chr4:2844741..2846381-chr4:2928922..2931560,2	MCF-7	breast:
12	chr4:2838331..2841092-chr4:2930392..2932648,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRK4-2	chr4:2930330-2930369	NONHSAT094823

No data

Variant related genes	Relation type
ADD1	TF binding region
ADD1	CpG island
ENSG00000087266	chromatin interactions
ENSG00000087274	chromatin interactions
ENSG00000180035	chromatin interactions

Extended variants
information (count: 214 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:214 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377611016	chr4:2927269-2927270	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs568370807	chr4:2927289-2927290	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs371437554	chr4:2927398-2927399	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs540227551	chr4:2927423-2927424	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs560524160	chr4:2927424-2927425	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs532723950	chr4:2927556-2927557	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs540980676	chr4:2927561-2927562	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs200560262	chr4:2927577-2927578	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs36207100	chr4:2927646-2927647	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs529807519	chr4:2927665-2927666	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs368083847	chr4:2927693-2927694	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs146879083	chr4:2927696-2927697	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs570272347	chr4:2927708-2927709	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs368842175	chr4:2927713-2927714	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs550266419	chr4:2927727-2927728	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs372316871	chr4:2927729-2927730	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs113953705	chr4:2927738-2927739	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs149239903	chr4:2927751-2927752	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs374663989	chr4:2927752-2927753	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs143465381	chr4:2927759-2927760	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs140746314	chr4:2927761-2927762	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs143366247	chr4:2927766-2927767	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs201305164	chr4:2927788-2927789	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs147536529	chr4:2927790-2927791	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs140040570	chr4:2927801-2927802	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs537595057	chr4:2927803-2927804	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs199501257	chr4:2927807-2927808	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs34021320	chr4:2927823-2927824	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs566457391	chr4:2927859-2927860	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs374946303	chr4:2927862-2927863	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs376731567	chr4:2927867-2927868	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs374428288	chr4:2927882-2927883	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs374440143	chr4:2927887-2927888	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs375445417	chr4:2927888-2927889	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs575512329	chr4:2927892-2927893	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs377066261	chr4:2927901-2927902	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs544392601	chr4:2927913-2927914	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs199593819	chr4:2927915-2927916	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs555115973	chr4:2927934-2927935	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs574869647	chr4:2927935-2927936	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs540701397	chr4:2927964-2927965	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs181876337	chr4:2927976-2927977	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs551677320	chr4:2927984-2927985	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs532529760	chr4:2927985-2927986	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs546098359	chr4:2928044-2928045	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs562798415	chr4:2928061-2928062	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs186250086	chr4:2928078-2928079	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs548342017	chr4:2928081-2928082	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs531461852	chr4:2928110-2928111	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs1263345	chr4:2928125-2928126	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Facial dysmorphism	22438245	CNVD
Wolf-Hirschhorn syndrome	22438245	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:186 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:2893200-2932600	Strong transcription	Fetal Thymus	thymus
2	chr4:2901200-2934600	Weak transcription	Hela-S3	cervix
3	chr4:2907400-2935400	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr4:2910600-2927800	Weak transcription	Small Intestine	intestine
5	chr4:2911200-2935000	Weak transcription	Psoas Muscle	Psoas
6	chr4:2912600-2934800	Weak transcription	A549	lung
7	chr4:2913000-2935000	Weak transcription	K562	blood
8	chr4:2915600-2933000	Weak transcription	Right Atrium	heart
9	chr4:2916400-2929800	Weak transcription	Fetal Heart	heart
10	chr4:2917000-2932000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
11	chr4:2918800-2927800	Weak transcription	Fetal Brain Male	brain
12	chr4:2923400-2932000	Strong transcription	Duodenum Mucosa	Duodenum
13	chr4:2923400-2932000	Strong transcription	Rectal Mucosa Donor 29	rectum
14	chr4:2923800-2933600	Strong transcription	Thymus	Thymus
15	chr4:2924000-2932000	Strong transcription	Fetal Muscle Leg	muscle
16	chr4:2924000-2934400	Strong transcription	Cortex derived primary cultured neurospheres	brain
17	chr4:2924200-2927400	Genic enhancers	Fetal Intestine Small	intestine
18	chr4:2924200-2927800	Genic enhancers	Fetal Intestine Large	intestine
19	chr4:2924200-2928200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr4:2924200-2928800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr4:2924200-2932000	Strong transcription	Sigmoid Colon	Sigmoid Colon
22	chr4:2924200-2932400	Strong transcription	Duodenum Smooth Muscle	Duodenum
23	chr4:2924200-2932600	Strong transcription	Rectal Smooth Muscle	rectum
24	chr4:2924200-2932600	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr4:2924200-2932800	Strong transcription	Adipose Nuclei	Adipose
26	chr4:2924200-2933000	Strong transcription	Rectal Mucosa Donor 31	rectum
27	chr4:2924200-2934400	Strong transcription	Fetal Stomach	stomach
28	chr4:2924200-2934800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr4:2924400-2932400	Strong transcription	Ovary	ovary
30	chr4:2924400-2933800	Strong transcription	Fetal Brain Female	brain
31	chr4:2924400-2934200	Strong transcription	Brain Germinal Matrix	brain
32	chr4:2924600-2932000	Strong transcription	Stomach Smooth Muscle	stomach
33	chr4:2924600-2932200	Strong transcription	Left Ventricle	heart
34	chr4:2924600-2932600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr4:2924800-2930400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr4:2924800-2931400	Strong transcription	Colonic Mucosa	Colon
37	chr4:2924800-2931600	Strong transcription	HepG2	liver
38	chr4:2924800-2931800	Strong transcription	Skeletal Muscle Male	skeletal muscle
39	chr4:2924800-2931800	Strong transcription	Skeletal Muscle Female	skeletal muscle
40	chr4:2924800-2933600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr4:2925000-2928800	Strong transcription	Placenta	Placenta
42	chr4:2925000-2931800	Strong transcription	Primary B cells from cord blood	blood
43	chr4:2925000-2932400	Strong transcription	Colon Smooth Muscle	Colon
44	chr4:2925000-2933800	Strong transcription	Dnd41	blood
45	chr4:2925000-2934400	Strong transcription	Osteobl	bone
46	chr4:2925200-2927600	Enhancers	Placenta Amnion	Placenta Amnion
47	chr4:2925200-2930200	Strong transcription	Primary neutrophils fromperipheralblood	blood
48	chr4:2925200-2932600	Strong transcription	Primary monocytes fromperipheralblood	blood
49	chr4:2925200-2932600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
50	chr4:2925200-2933200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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