Variant report

Variant	esv14797
Chromosome Location	chr4:1289224-1292044
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:51)
CpG islands
(count:183)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:51 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD2	chr4:1291724-1291883	H1-hESC	embryonic stem cell:	n/a	n/a
2	EBF1	chr4:1289571-1289819	GM12878	blood:	n/a	n/a
3	GTF2F1	chr4:1291717-1291769	H1-hESC	embryonic stem cell:	n/a	n/a
4	MAX	chr4:1291542-1292061	H1-hESC	embryonic stem cell:	n/a	n/a
5	MAX	chr4:1291541-1291968	ECC-1	luminal epithelium:	n/a	n/a
6	MYC	chr4:1289798-1289801	MCF-7	breast:	n/a	n/a
7	MYC	chr4:1289840-1289855	MCF-7	breast:	n/a	n/a
8	POLR2A	chr4:1291190-1291674	HepG2	liver:	n/a	n/a
9	POLR2A	chr4:1291362-1291394	GM12878	blood:	n/a	n/a
10	POLR2A	chr4:1290440-1291012	K562	blood:	n/a	n/a
11	POLR2A	chr4:1289931-1289990	HepG2	liver:	n/a	n/a
12	POLR2A	chr4:1290576-1290608	K562	blood:	n/a	n/a
13	POLR2A	chr4:1289945-1290008	ProgFib	skin:	n/a	n/a
14	POLR2A	chr4:1289624-1289825	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr4:1289352-1289398	K562	blood:	n/a	n/a
16	POLR2A	chr4:1291917-1291936	GM12878	blood:	n/a	n/a
17	POLR2A	chr4:1290511-1290565	K562	blood:	n/a	n/a
18	POLR2A	chr4:1290890-1291590	K562	blood:	n/a	n/a
19	POLR2A	chr4:1290613-1290667	K562	blood:	n/a	n/a
20	POLR2A	chr4:1289669-1289795	GM12878	blood:	n/a	n/a
21	POLR2A	chr4:1290893-1291068	GM12878	blood:	n/a	n/a
22	POLR2A	chr4:1289188-1289254	K562	blood:	n/a	n/a
23	POLR2A	chr4:1291554-1291895	K562	blood:	n/a	n/a
24	POLR2A	chr4:1290513-1292103	K562	blood:	n/a	n/a
25	POLR2A	chr4:1291162-1291164	K562	blood:	n/a	n/a
26	POLR2A	chr4:1291653-1291665	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr4:1290153-1290458	K562	blood:	n/a	n/a
28	POLR2A	chr4:1289336-1289337	K562	blood:	n/a	n/a
29	POLR2A	chr4:1291717-1291724	K562	blood:	n/a	n/a
30	POLR2A	chr4:1289803-1290003	K562	blood:	n/a	n/a
31	POLR2A	chr4:1289261-1289322	K562	blood:	n/a	n/a
32	POLR2A	chr4:1291733-1291927	K562	blood:	n/a	n/a
33	POLR2A	chr4:1290789-1292001	K562	blood:	n/a	n/a
34	POLR2A	chr4:1290939-1291735	GM12878	blood:	n/a	n/a
35	POLR2A	chr4:1291943-1292029	HepG2	liver:	n/a	n/a
36	POLR2A	chr4:1289123-1289249	K562	blood:	n/a	n/a
37	POLR2A	chr4:1291680-1291735	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr4:1291889-1292124	K562	blood:	n/a	n/a
39	POLR2A	chr4:1289632-1290130	K562	blood:	n/a	n/a
40	POLR2A	chr4:1291180-1291237	K562	blood:	n/a	n/a
41	POLR2A	chr4:1288600-1289797	K562	blood:	n/a	n/a
42	POLR2A	chr4:1291751-1291754	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr4:1291593-1291628	K562	blood:	n/a	n/a
44	SIN3A	chr4:1291592-1291647	H1-hESC	embryonic stem cell:	n/a	n/a
45	TBP	chr4:1291598-1291605	H1-hESC	embryonic stem cell:	n/a	n/a
46	TEAD4	chr4:1291482-1291999	H1-hESC	embryonic stem cell:	n/a	n/a
47	TEAD4	chr4:1291505-1291971	H1-hESC	embryonic stem cell:	n/a	n/a
48	ZEB1	chr4:1289153-1289818	GM12878	blood:	n/a	chr4:1289484-1289493
49	ZEB1	chr4:1290142-1290365	GM12878	blood:	n/a	chr4:1290196-1290203 chr4:1290291-1290300
50	ZEB1	chr4:1289532-1289798	GM12878	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:1291382-1291432	HNPCEpiC	eye:	n/a
2	chr4:1291382-1291432	HL-60	blood:	n/a
3	chr4:1291382-1291432	Jurkat	blood:	n/a
4	chr4:1291382-1291432	Hela-S3	cervix:	n/a
5	chr4:1290568-1290618	HEEpiC	esophagus:	n/a
6	chr4:1290568-1290618	HRPEpiC	eye:	n/a
7	chr4:1290568-1290618	AG09319	gingival:	n/a
8	chr4:1291382-1291432	GM19239	blood:	n/a
9	chr4:1290568-1290618	HCPEpiC	choroid plexus:	n/a
10	chr4:1290568-1290618	ECC-1	luminal epithelium:	n/a
11	chr4:1291076-1291126	T-47D	breast:	n/a
12	chr4:1291076-1291126	HAEpiC	amniotic membrane:	n/a
13	chr4:1291076-1291126	GM12878	blood:	n/a
14	chr4:1290568-1290618	K562	blood:	n/a
15	chr4:1291076-1291126	A549	lung:	n/a
16	chr4:1291382-1291432	NHDF-neo	bronchial:	n/a
17	chr4:1291076-1291126	BJ	skin:	n/a
18	chr4:1291076-1291126	K562	blood:	n/a
19	chr4:1291076-1291126	HUVEC	blood vessel:	n/a
20	chr4:1291382-1291432	HMEC	breast:	n/a
21	chr4:1291076-1291126	LNCaP	prostate:	n/a
22	chr4:1291382-1291432	HRCEpiC	kidney:	n/a
23	chr4:1291076-1291126	HRE	kidney:	n/a
24	chr4:1290568-1290618	ProgFib	skin:	n/a
25	chr4:1291382-1291432	HEK293	kidney:	embryo
26	chr4:1291076-1291126	NT2-D1	testis:	n/a
27	chr4:1291382-1291432	SKMC	muscle:	n/a
28	chr4:1291076-1291126	NHDF-neo	bronchial:	n/a
29	chr4:1290568-1290618	HepG2	liver:	n/a
30	chr4:1291076-1291126	NH-A	brain:	n/a
31	chr4:1291382-1291432	HCT-116	colon:	n/a
32	chr4:1290568-1290618	CMK	blood:	n/a
33	chr4:1291076-1291126	PFSK-1	brain:	n/a
34	chr4:1290568-1290618	GM12892	blood:	n/a
35	chr4:1291382-1291432	GM12891	blood:	n/a
36	chr4:1291382-1291432	ovcar-3	ovarian:	n/a
37	chr4:1291076-1291126	ECC-1	luminal epithelium:	n/a
38	chr4:1290568-1290618	RPTEC	kidney:	n/a
39	chr4:1291076-1291126	CMK	blood:	n/a
40	chr4:1290568-1290618	U87	brain:	n/a
41	chr4:1291076-1291126	HepG2	liver:	n/a
42	chr4:1291076-1291126	Jurkat	blood:	n/a
43	chr4:1291076-1291126	HPAEpiC	pulmonary alveolar:	n/a
44	chr4:1291382-1291432	ProgFib	skin:	n/a
45	chr4:1291382-1291432	NH-A	brain:	n/a
46	chr4:1290568-1290618	Caco-2	colon:	n/a
47	chr4:1290568-1290618	Jurkat	blood:	n/a
48	chr4:1291076-1291126	AG04450	lung:	fetal
49	chr4:1291382-1291432	CMK	blood:	n/a
50	chr4:1290568-1290618	Hepatocyte	liver:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:1288933..1290698-chr4:1333775..1336445,2	K562	blood:
2	chr4:1289122..1291329-chr4:1338444..1340407,2	MCF-7	breast:
3	chr4:1242309..1244859-chr4:1287604..1289236,2	MCF-7	breast:
4	chr4:1287434..1290416-chr4:1342936..1345119,2	K562	blood:
5	chr4:1036618..1039246-chr4:1287884..1290247,2	K562	blood:
6	chr4:1236923..1239811-chr4:1291885..1294129,2	K562	blood:
7	chr4:1236833..1250005-chr4:1276188..1292579,54	MCF-7	breast:
8	chr4:1241391..1244976-chr4:1289369..1292052,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C4orf42-4	chr4:1291858-1291903	NONHSAT094696

No data

Variant related genes	Relation type
MAEA	TF binding region
MAEA	CpG island
ENSG00000159692	chromatin interactions
ENSG00000196810	chromatin interactions

Extended variants
information (count: 185 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:185 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569105387	chr4:1289234-1289235	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs536158359	chr4:1289258-1289259	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs547967832	chr4:1289260-1289261	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs374846948	chr4:1289336-1289337	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs373561845	chr4:1289345-1289346	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs367780968	chr4:1289366-1289367	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs566359563	chr4:1289402-1289403	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs386670478	chr4:1289427-1289428	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs182221945	chr4:1289446-1289447	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs113718520	chr4:1289447-1289448	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs202041097	chr4:1289455-1289456	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs73069985	chr4:1289462-1289463	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs140973910	chr4:1289475-1289476	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs369222591	chr4:1289496-1289497	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs186050039	chr4:1289500-1289501	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs111294586	chr4:1289507-1289508	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs191459307	chr4:1289508-1289509	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs144698785	chr4:1289510-1289511	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs138613290	chr4:1289516-1289517	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs201116206	chr4:1289521-1289522	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs368095956	chr4:1289522-1289523	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs183223582	chr4:1289525-1289526	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs199963263	chr4:1289536-1289537	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs188866759	chr4:1289548-1289549	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs572282252	chr4:1289561-1289562	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs112682311	chr4:1289562-1289563	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs112613444	chr4:1289566-1289567	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs543250269	chr4:1289571-1289572	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs149267883	chr4:1289572-1289573	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs117476122	chr4:1289610-1289611	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs79289407	chr4:1289611-1289612	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs543375237	chr4:1289629-1289630	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs114981738	chr4:1289673-1289674	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs193043147	chr4:1289736-1289737	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs185305831	chr4:1289739-1289740	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs137969700	chr4:1289758-1289759	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs540482132	chr4:1289764-1289765	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs376728033	chr4:1289773-1289774	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs565336180	chr4:1289813-1289814	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs369002852	chr4:1289888-1289889	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs531988706	chr4:1289920-1289921	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs550208315	chr4:1289923-1289924	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs565248140	chr4:1289940-1289941	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs532586715	chr4:1289944-1289945	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs71168821	chr4:1289964-1289965	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs201628544	chr4:1289975-1289976	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs547893103	chr4:1290010-1290011	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs369697185	chr4:1290089-1290090	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs550917874	chr4:1290137-1290138	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs562777980	chr4:1290154-1290155	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Breast cancer	17142309	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	20932292	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Type 2 diabetes	21754918	CNVD

Chromatin state (count:341 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:1284600-1290200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr4:1285000-1289400	Enhancers	Primary T helper naive cells from peripheral blood	blood
3	chr4:1285200-1290200	Weak transcription	Aorta	Aorta
4	chr4:1285200-1293800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr4:1285200-1303400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:1285400-1289400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr4:1285400-1290200	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr4:1285400-1290600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr4:1285400-1291200	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr4:1285400-1291200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr4:1285400-1293400	Weak transcription	A549	lung
12	chr4:1285400-1294200	Weak transcription	HSMMtube	muscle
13	chr4:1285400-1294200	Weak transcription	HUVEC	blood vessel
14	chr4:1285400-1302400	Weak transcription	Fetal Kidney	kidney
15	chr4:1285600-1289400	Genic enhancers	Primary neutrophils fromperipheralblood	blood
16	chr4:1285600-1290200	Weak transcription	Fetal Lung	lung
17	chr4:1285600-1290600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr4:1285600-1291400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr4:1285800-1296000	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr4:1285800-1302200	Weak transcription	NHDF-Ad	bronchial
21	chr4:1286000-1289400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr4:1286000-1289400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr4:1286000-1295200	Strong transcription	Thymus	Thymus
24	chr4:1286200-1290200	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr4:1286200-1290800	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr4:1286200-1291400	Weak transcription	Hela-S3	cervix
27	chr4:1286200-1293400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:1286200-1299200	Strong transcription	Fetal Intestine Small	intestine
29	chr4:1286200-1302400	Weak transcription	Fetal Brain Male	brain
30	chr4:1286400-1289400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr4:1286400-1290600	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr4:1286400-1299000	Weak transcription	Small Intestine	intestine
33	chr4:1286600-1290200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr4:1286600-1290200	Weak transcription	NHLF	lung
35	chr4:1287000-1289400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr4:1287200-1289400	Enhancers	Fetal Heart	heart
37	chr4:1287200-1289400	Enhancers	Left Ventricle	heart
38	chr4:1287200-1289400	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr4:1287200-1290400	Enhancers	Right Atrium	heart
40	chr4:1287400-1289400	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr4:1287400-1289400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr4:1287400-1289400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr4:1287400-1289400	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr4:1287400-1289400	Enhancers	Adipose Nuclei	Adipose
45	chr4:1287400-1289400	Enhancers	Liver	Liver
46	chr4:1287400-1289400	Genic enhancers	Brain Anterior Caudate	brain
47	chr4:1287400-1289400	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr4:1287400-1289400	Genic enhancers	Lung	lung
49	chr4:1287400-1289800	Genic enhancers	Fetal Muscle Trunk	muscle
50	chr4:1287400-1291800	Genic enhancers	Gastric	stomach

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