Variant report

Variant	nsv878271
Chromosome Location	chr4:803637-828148
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:595)
CpG islands
(count:1405)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:595 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:809427-810025	HepG2	liver:	n/a	n/a
2	BACH1	chr4:819446-819522	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr4:819894-819984	K562	blood:	n/a	n/a
4	BHLHE40	chr4:819415-819463	K562	blood:	n/a	n/a
5	BHLHE40	chr4:815716-815913	K562	blood:	n/a	n/a
6	CBX3	chr4:825446-826136	K562	blood:	n/a	n/a
7	CBX3	chr4:825728-826011	K562	blood:	n/a	n/a
8	CCNT2	chr4:819783-819973	K562	blood:	n/a	chr4:819957-819966
9	CCNT2	chr4:819353-819529	K562	blood:	n/a	n/a
10	CEBPB	chr4:809361-809780	HepG2	liver:	n/a	n/a
11	CEBPB	chr4:809490-809723	HepG2	liver:	n/a	n/a
12	CEBPB	chr4:822668-822978	Hela-S3	cervix:	n/a	n/a
13	CHD2	chr4:819901-820071	Hela-S3	cervix:	n/a	chr4:819955-819965
14	CHD2	chr4:820804-820813	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr4:809424-809698	HepG2	liver:	n/a	n/a
16	CHD2	chr4:822480-822935	Hela-S3	cervix:	n/a	n/a
17	CREB1	chr4:819832-820160	HepG2	liver:	n/a	n/a
18	CREB1	chr4:819784-820055	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr4:819757-820087	K562	blood:	n/a	n/a
20	CTBP2	chr4:818452-819542	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTBP2	chr4:820592-820908	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr4:822880-823030	GM06990	blood:	n/a	n/a
23	CTCF	chr4:809220-809370	HepG2	liver:	n/a	n/a
24	CTCF	chr4:824900-825050	HepG2	liver:	n/a	chr4:825010-825023
25	CTCF	chr4:818200-818350	GM12871	blood:	n/a	n/a
26	CTCF	chr4:822760-822910	AG04449	skin:	n/a	n/a
27	CTCF	chr4:807800-807950	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr4:822460-822610	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr4:807760-807910	SAEC	small airway:	n/a	n/a
30	CTCF	chr4:818118-818236	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr4:807740-807890	GM12866	blood:	n/a	n/a
32	CTCF	chr4:822720-822870	GM12874	blood:	n/a	n/a
33	CTCF	chr4:818240-818390	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr4:818040-818190	GM12874	blood:	n/a	chr4:818100-818113
35	CTCF	chr4:822760-822910	BJ	skin:	n/a	n/a
36	CTCF	chr4:818314-818379	GM19240	blood:	n/a	n/a
37	CTCF	chr4:818055-818222	Fibrobl	skin:	n/a	chr4:818100-818113
38	CTCF	chr4:822780-822930	HPF	lung:	n/a	n/a
39	CTCF	chr4:822720-822870	HCT-116	colon:	n/a	n/a
40	CTCF	chr4:818104-818173	ProgFib	skin:	n/a	n/a
41	CTCF	chr4:822800-822950	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chr4:807643-808042	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:817708-817800	Fibrobl	skin:	n/a	n/a
44	CTCF	chr4:807780-807930	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr4:807760-807910	HMF	breast:	n/a	n/a
46	CTCF	chr4:822819-822946	ProgFib	skin:	n/a	n/a
47	CTCF	chr4:807800-807950	Caco-2	colon:	n/a	n/a
48	CTCF	chr4:807740-807890	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr4:822780-822930	GM12865	blood:	n/a	n/a
50	CTCF	chr4:807860-808010	GM12868	blood:	n/a	n/a

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:815269-815319	IMR90	lung:	fetal
2	chr4:820756-820806	HCF	heart:	n/a
3	chr4:815269-815319	IMR90	lung:	fetal
4	chr4:820756-820806	HCF	heart:	n/a
5	chr4:809452-809502	ProgFib	skin:	n/a
6	chr4:820619-820669	HCPEpiC	choroid plexus:	n/a
7	chr4:819227-819277	HNPCEpiC	eye:	n/a
8	chr4:827675-827725	MCF-7	breast:	n/a
9	chr4:821075-821125	NHDF-neo	bronchial:	n/a
10	chr4:827675-827725	Hepatocyte	liver:	n/a
11	chr4:827675-827725	HEK293	kidney:	embryo
12	chr4:812499-812549	GM12878	blood:	n/a
13	chr4:828098-828148	U87	brain:	n/a
14	chr4:819927-819977	HAEpiC	amniotic membrane:	n/a
15	chr4:811641-811691	HRE	kidney:	n/a
16	chr4:814948-814998	BJ	skin:	n/a
17	chr4:817492-817542	HUVEC	blood vessel:	n/a
18	chr4:817492-817542	HCM	heart:	n/a
19	chr4:819227-819277	HUVEC	blood vessel:	n/a
20	chr4:812499-812549	AG09319	gingival:	n/a
21	chr4:828098-828148	HUVEC	blood vessel:	n/a
22	chr4:814948-814998	Hela-S3	cervix:	n/a
23	chr4:812387-812437	HCM	heart:	n/a
24	chr4:812387-812437	LNCaP	prostate:	n/a
25	chr4:817492-817542	Hepatocyte	liver:	n/a
26	chr4:812499-812549	GM12892	blood:	n/a
27	chr4:824416-824466	SK-N-SH_RA	brain:	n/a
28	chr4:815098-815148	Jurkat	blood:	n/a
29	chr4:819151-819201	Hela-S3	cervix:	n/a
30	chr4:821075-821125	HCM	heart:	n/a
31	chr4:811641-811691	AG09319	gingival:	n/a
32	chr4:816935-816985	AoSMC	blood vessel:	n/a
33	chr4:812611-812661	HEEpiC	esophagus:	n/a
34	chr4:827675-827725	PANC-1	pancreas:	n/a
35	chr4:812387-812437	A549	lung:	n/a
36	chr4:816968-817018	HRPEpiC	eye:	n/a
37	chr4:817492-817542	HRE	kidney:	n/a
38	chr4:827675-827725	AG09319	gingival:	n/a
39	chr4:814948-814998	HAEpiC	amniotic membrane:	n/a
40	chr4:817492-817542	GM12891	blood:	n/a
41	chr4:812499-812549	SAEC	small airway:	n/a
42	chr4:815098-815148	AG09319	gingival:	n/a
43	chr4:828098-828148	HPAEpiC	pulmonary alveolar:	n/a
44	chr4:819151-819201	BJ	skin:	n/a
45	chr4:811641-811691	HCF	heart:	n/a
46	chr4:811981-812031	LNCaP	prostate:	n/a
47	chr4:828098-828148	BE2_C	brain:	n/a
48	chr4:821075-821125	HRPEpiC	eye:	n/a
49	chr4:820619-820669	K562	blood:	n/a
50	chr4:820619-820669	Hepatocyte	liver:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:770559..774303-chr4:822047..825549,3	MCF-7	breast:
2	chr4:801291..803192-chr4:806051..807606,2	MCF-7	breast:
3	chr4:775742..777793-chr4:821294..823838,2	MCF-7	breast:
4	chr4:779184..781836-chr4:815756..818416,2	MCF-7	breast:
5	chr4:811397..815674-chr4:816390..820314,6	K562	blood:
6	chr4:796709..798634-chr4:802250..803920,2	MCF-7	breast:
7	chr4:822237..824857-chr4:826820..829457,3	MCF-7	breast:
8	chr4:827937..829545-chr4:861897..864228,2	K562	blood:
9	chr4:810119..812562-chr4:817081..819359,3	MCF-7	breast:
10	chr4:773678..778564-chr4:818343..821273,5	K562	blood:
11	chr4:808238..810309-chr4:818113..820834,2	MCF-7	breast:
12	chr4:814287..815828-chr4:819004..820949,2	MCF-7	breast:
13	chr4:675798..677554-chr4:822582..825253,2	K562	blood:
14	chr4:810119..812562-chr4:817081..819359,3	MCF-7	breast:
15	chr4:807624..808191-chr4:885316..885983,2	MCF-7	breast:
16	chr4:723282..726108-chr4:810901..813432,2	K562	blood:
17	chr4:782997..785390-chr4:814047..817037,2	K562	blood:
18	chr4:807835..809615-chr4:815681..817345,2	MCF-7	breast:
19	chr4:767045..769488-chr4:820601..823147,2	K562	blood:
20	chr4:821558..823207-chr4:827876..830795,2	MCF-7	breast:
21	chr4:827903..829501-chr4:976207..978767,2	MCF-7	breast:
22	chr4:813382..814362-chr8:22941603..22942165,2	HCT-116	colon:
23	chr4:812550..814672-chr4:1242293..1245103,2	K562	blood:
24	chr4:800740..802863-chr4:815216..816948,2	K562	blood:
25	chr4:802679..805389-chr4:828625..831551,2	K562	blood:
26	chr4:809375..810958-chr4:813347..815488,2	MCF-7	breast:
27	chr4:816506..819302-chr4:925651..929828,3	K562	blood:
28	chr4:822237..824857-chr4:826820..829457,3	MCF-7	breast:
29	chr4:814299..816163-chr4:965905..968513,2	MCF-7	breast:
30	chr4:774284..777559-chr4:817781..820963,6	MCF-7	breast:
31	chr4:813190..814907-chr4:985263..987918,2	MCF-7	breast:
32	chr4:776936..779756-chr4:805592..808402,2	MCF-7	breast:
33	chr4:815070..817280-chr4:1004466..1007388,2	K562	blood:
34	chr4:821558..823207-chr4:827876..830795,2	MCF-7	breast:
35	chr4:774600..776283-chr4:806422..808512,2	MCF-7	breast:
36	chr4:807835..809615-chr4:815681..817345,2	MCF-7	breast:
37	chr4:820499..822225-chr4:975841..977924,2	K562	blood:
38	chr4:809375..810958-chr4:813347..815488,2	MCF-7	breast:

No data

Variant related genes	Relation type
CPLX1	TF binding region
CPLX1	CpG island
ENSG00000159692	chromatin interactions
ENSG00000185619	chromatin interactions
ENSG00000173535	chromatin interactions
ENSG00000127419	chromatin interactions
ENSG00000196810	chromatin interactions
ENSG00000145214	chromatin interactions
ENSG00000260262	chromatin interactions
ENSG00000127415	chromatin interactions
ENSG00000127418	chromatin interactions
ENSG00000168993	chromatin interactions
ENSG00000178950	chromatin interactions
ENSG00000145217	chromatin interactions
ENSG00000249592	chromatin interactions

Extended variants
information (count: 1117 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1117 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28504502	chr4:803637-803638	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs370160153	chr4:803656-803657	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs189136667	chr4:803661-803662	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs191925984	chr4:803670-803671	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs527878506	chr4:803682-803683	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs535861084	chr4:803683-803684	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs557446578	chr4:803699-803700	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs138349524	chr4:803715-803716	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs550100945	chr4:803735-803736	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs28532973	chr4:803763-803764	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs529446451	chr4:803775-803776	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs56195046	chr4:803835-803836	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs552607880	chr4:803836-803837	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs547907667	chr4:803844-803845	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs71166896	chr4:803855-803856	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs565910488	chr4:803868-803869	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs539626739	chr4:803869-803870	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs551400839	chr4:803876-803877	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs569905196	chr4:803877-803878	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs536647105	chr4:803898-803899	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs555303499	chr4:803899-803900	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs573292969	chr4:803900-803901	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs537211535	chr4:803924-803925	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs552632413	chr4:803975-803976	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs572341408	chr4:803978-803979	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs546346717	chr4:803982-803983	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs564625488	chr4:803985-803986	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs558704430	chr4:803994-803995	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs576634629	chr4:804000-804001	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs577007885	chr4:804027-804028	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs543746354	chr4:804039-804040	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs562157556	chr4:804059-804060	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs369127019	chr4:804060-804061	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs541306435	chr4:804073-804074	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184485835	chr4:804096-804097	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs559850000	chr4:804116-804117	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs533185321	chr4:804127-804128	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs551507656	chr4:804128-804129	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs115788968	chr4:804129-804130	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs537392239	chr4:804132-804133	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs549006555	chr4:804143-804144	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs574046911	chr4:804146-804147	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs56301015	chr4:804157-804158	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs187015073	chr4:804170-804171	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs56296967	chr4:804187-804188	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs79822845	chr4:804236-804237	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs377104769	chr4:804277-804278	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs144353088	chr4:804285-804286	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs577269239	chr4:804288-804289	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs539650954	chr4:804364-804365	Weak transcription	Chromatin interactive region	1 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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:789600-816800	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr4:802200-803800	Enhancers	Fetal Brain Male	brain
3	chr4:803000-803800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
4	chr4:803400-807600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr4:804800-805200	Bivalent Enhancer	HepG2	liver
6	chr4:806400-806600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr4:807600-807800	Bivalent Enhancer	HepG2	liver
8	chr4:807800-808000	Enhancers	Esophagus	oesophagus
9	chr4:807800-809200	Enhancers	HepG2	liver
10	chr4:808000-808200	Bivalent Enhancer	Duodenum Mucosa	Duodenum
11	chr4:808200-808400	Enhancers	Gastric	stomach
12	chr4:808200-811000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr4:808400-809200	Weak transcription	Gastric	stomach
14	chr4:808600-808800	Bivalent Enhancer	Fetal Stomach	stomach
15	chr4:808600-809600	Enhancers	Colonic Mucosa	Colon
16	chr4:808600-810000	Enhancers	Fetal Intestine Large	intestine
17	chr4:808600-811600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr4:809200-809400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
19	chr4:809200-809400	Bivalent Enhancer	Fetal Lung	lung
20	chr4:809200-809400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
21	chr4:809200-809400	Bivalent Enhancer	Fetal Muscle Leg	muscle
22	chr4:809200-809400	Enhancers	Gastric	stomach
23	chr4:809200-809600	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
24	chr4:809200-809600	Enhancers	Stomach Mucosa	stomach
25	chr4:809200-809800	Enhancers	Rectal Mucosa Donor 29	rectum
26	chr4:809200-810000	Enhancers	Liver	Liver
27	chr4:809200-810000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
28	chr4:809200-810000	Flanking Active TSS	HepG2	liver
29	chr4:809400-809600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr4:809400-809600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr4:809400-809600	Flanking Active TSS	Pancreas	Pancrea
32	chr4:809400-809600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
33	chr4:809400-809800	Enhancers	Duodenum Smooth Muscle	Duodenum
34	chr4:809400-809800	Bivalent Enhancer	A549	lung
35	chr4:809400-817200	Weak transcription	Brain Angular Gyrus	brain
36	chr4:809600-809800	Enhancers	Pancreas	Pancrea
37	chr4:809600-811000	Enhancers	Colon Smooth Muscle	Colon
38	chr4:810000-811000	Enhancers	HepG2	liver
39	chr4:811600-813800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr4:812000-812200	Bivalent Enhancer	HepG2	liver
41	chr4:813800-814400	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
42	chr4:814400-815800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr4:814800-815000	Bivalent Enhancer	Placenta	Placenta
44	chr4:815400-819200	Bivalent Enhancer	Fetal Brain Male	brain
45	chr4:815600-816000	Bivalent Enhancer	Brain Germinal Matrix	brain
46	chr4:815800-816000	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
47	chr4:815800-816000	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
48	chr4:815800-816000	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
49	chr4:816000-816200	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
50	chr4:816000-817000	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain

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