Variant report

Variant	nsv593624
Chromosome Location	chr4:8026176-8047973
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:221)
CpG islands
(count:307)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:221 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr4:8038912-8039504	GM12878	blood:	n/a	n/a
2	BCL3	chr4:8029949-8030517	GM12878	blood:	n/a	n/a
3	BCL3	chr4:8029834-8030570	GM12878	blood:	n/a	n/a
4	BCL3	chr4:8039082-8039561	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:8042425-8042692	HepG2	liver:	n/a	n/a
6	BHLHE40	chr4:8042424-8042710	K562	blood:	n/a	n/a
7	BRCA1	chr4:8030194-8030478	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr4:8034949-8035108	HepG2	liver:	n/a	n/a
9	CTCF	chr4:8032242-8032380	NHEK	skin:	n/a	n/a
10	CTCF	chr4:8047783-8047850	MCF-7	breast:	n/a	n/a
11	CTCF	chr4:8037220-8037370	HCPEpiC	choroid plexus:	n/a	n/a
12	CTCF	chr4:8047705-8047903	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr4:8047720-8047870	A549	lung:	n/a	n/a
14	CTCF	chr4:8037349-8037405	HUVEC	blood vessel:	n/a	n/a
15	CTCF	chr4:8047680-8047830	Caco-2	colon:	n/a	n/a
16	CTCF	chr4:8032220-8032370	HMEC	breast:	n/a	n/a
17	CTCF	chr4:8037280-8037430	HMEC	breast:	n/a	n/a
18	CTCF	chr4:8026060-8026210	GM12875	blood:	n/a	n/a
19	CTCF	chr4:8032240-8032390	NHEK	skin:	n/a	n/a
20	CTCF	chr4:8041080-8041230	BE2_C	brain:	n/a	chr4:8041108-8041126
21	CTCF	chr4:8032260-8032410	HMEC	breast:	n/a	n/a
22	CTCF	chr4:8036787-8036833	GM19239	blood:	n/a	n/a
23	CTCF	chr4:8036142-8036227	GM19239	blood:	n/a	n/a
24	CTCF	chr4:8039850-8039927	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr4:8031020-8031170	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr4:8047758-8047824	A549	lung:	n/a	n/a
27	CTCF	chr4:8047680-8047830	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr4:8036329-8036516	GM19239	blood:	n/a	n/a
29	CTCF	chr4:8047740-8047890	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr4:8041080-8041230	SK-N-SH_RA	brain:	n/a	chr4:8041108-8041126
31	CTCF	chr4:8047640-8047790	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr4:8047600-8047750	NB4	blood:	n/a	n/a
33	CTCF	chr4:8037340-8037490	AG09309	skin:	n/a	n/a
34	CTCF	chr4:8047760-8047910	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr4:8039852-8039902	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr4:8037348-8037444	Gliobla	brain:	n/a	n/a
37	CTCF	chr4:8037280-8037430	HA-sp	spinal cord:	n/a	n/a
38	CTCF	chr4:8047700-8047850	HepG2	liver:	n/a	n/a
39	CTCF	chr4:8037280-8037430	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr4:8039860-8040010	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr4:8039826-8039909	GM12891	blood:	n/a	n/a
42	CTCF	chr4:8027622-8027663	Pancreas_OC	pancreas:	n/a	n/a
43	CTCF	chr4:8037240-8037390	NB4	blood:	n/a	n/a
44	CTCF	chr4:8037160-8037310	HCM	heart:	n/a	n/a
45	CTCF	chr4:8037260-8037410	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr4:8047623-8047857	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr4:8047764-8047834	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr4:8036321-8036328	GM19239	blood:	n/a	n/a
49	CTCF	chr4:8047740-8047890	Caco-2	colon:	n/a	n/a
50	CTCF	chr4:8037370-8037401	GM19239	blood:	n/a	n/a

(count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8046547-8046597	HCF	heart:	n/a
2	chr4:8034335-8034385	PFSK-1	brain:	n/a
3	chr4:8046547-8046597	HCF	heart:	n/a
4	chr4:8034335-8034385	PFSK-1	brain:	n/a
5	chr4:8046793-8046843	HL-60	blood:	n/a
6	chr4:8046793-8046843	GM12891	blood:	n/a
7	chr4:8034100-8034150	HEK293	kidney:	embryo
8	chr4:8034335-8034385	K562	blood:	n/a
9	chr4:8046793-8046843	NT2-D1	testis:	n/a
10	chr4:8037325-8037375	GM06990	blood:	n/a
11	chr4:8046547-8046597	HRE	kidney:	n/a
12	chr4:8034335-8034385	AG04450	lung:	fetal
13	chr4:8037325-8037375	NH-A	brain:	n/a
14	chr4:8046793-8046843	K562	blood:	n/a
15	chr4:8034335-8034385	HEK293	kidney:	embryo
16	chr4:8034100-8034150	SK-N-SH_RA	brain:	n/a
17	chr4:8046793-8046843	LNCaP	prostate:	n/a
18	chr4:8046547-8046597	PFSK-1	brain:	n/a
19	chr4:8034335-8034385	PANC-1	pancreas:	n/a
20	chr4:8034335-8034385	GM12878	blood:	n/a
21	chr4:8046547-8046597	HepG2	liver:	n/a
22	chr4:8034100-8034150	HRCEpiC	kidney:	n/a
23	chr4:8034335-8034385	AG09309	skin:	n/a
24	chr4:8034100-8034150	NHDF-neo	bronchial:	n/a
25	chr4:8034335-8034385	ECC-1	luminal epithelium:	n/a
26	chr4:8046793-8046843	MCF-7	breast:	n/a
27	chr4:8046793-8046843	MCF10A-Er-Src	breast:	n/a
28	chr4:8034100-8034150	SAEC	small airway:	n/a
29	chr4:8034335-8034385	MCF-7	breast:	n/a
30	chr4:8046547-8046597	T-47D	breast:	n/a
31	chr4:8037325-8037375	AG04449	skin:	fetal
32	chr4:8037325-8037375	PANC-1	pancreas:	n/a
33	chr4:8046793-8046843	HRE	kidney:	n/a
34	chr4:8046547-8046597	BJ	skin:	n/a
35	chr4:8046547-8046597	RPTEC	kidney:	n/a
36	chr4:8034100-8034150	AG04450	lung:	fetal
37	chr4:8034100-8034150	AG04449	skin:	fetal
38	chr4:8046793-8046843	PANC-1	pancreas:	n/a
39	chr4:8034100-8034150	CMK	blood:	n/a
40	chr4:8034100-8034150	AG09319	gingival:	n/a
41	chr4:8037325-8037375	LNCaP	prostate:	n/a
42	chr4:8034335-8034385	HPAEpiC	pulmonary alveolar:	n/a
43	chr4:8034335-8034385	HCM	heart:	n/a
44	chr4:8046547-8046597	HNPCEpiC	eye:	n/a
45	chr4:8046547-8046597	PrEC	prostate:	n/a
46	chr4:8046793-8046843	A549	lung:	n/a
47	chr4:8034100-8034150	SK-N-SH	brain:	n/a
48	chr4:8037325-8037375	AG09319	gingival:	n/a
49	chr4:8034335-8034385	HRE	kidney:	n/a
50	chr4:8046547-8046597	AG04449	skin:	fetal

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:8019333..8020892-chr4:8033325..8035259,2	MCF-7	breast:
2	chr4:8034585..8036214-chr4:8037779..8039313,2	MCF-7	breast:
3	chr4:8034679..8036492-chr4:8044258..8047037,2	K562	blood:
4	chr4:8027811..8029629-chr4:8031244..8032843,2	K562	blood:
5	chr4:8020482..8023593-chr4:8027718..8031223,3	MCF-7	breast:
6	chr4:8024330..8026063-chr4:8034890..8037450,2	MCF-7	breast:
7	chr4:8021380..8023890-chr4:8026077..8027621,2	MCF-7	breast:
8	chr4:8030441..8032567-chr4:8033404..8037009,3	K562	blood:
9	chr4:8030886..8034532-chr4:8039153..8041983,3	MCF-7	breast:
10	chr4:8021662..8023195-chr4:8024850..8026832,2	K562	blood:
11	chr4:8030441..8032567-chr4:8033404..8037009,3	K562	blood:
12	chr4:8033575..8035551-chr4:8063220..8065289,2	K562	blood:
13	chr4:8027811..8029629-chr4:8031244..8032843,2	K562	blood:
14	chr4:8034585..8036214-chr4:8037779..8039313,2	MCF-7	breast:
15	chr4:8039157..8040706-chr4:8050002..8052437,2	K562	blood:
16	chr4:8030886..8034532-chr4:8039153..8041983,3	MCF-7	breast:
17	chr4:8034679..8036492-chr4:8044258..8047037,2	K562	blood:
18	chr4:8019469..8024052-chr4:8025659..8029825,5	MCF-7	breast:

No data

Variant related genes	Relation type
ABLIM2	TF binding region
ABLIM2	CpG island
ENSG00000273267	chromatin interactions
ENSG00000163995	chromatin interactions

Extended variants
information (count: 1174 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1174 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11729381	chr4:8026176-8026177	Enhancers Bivalent Enhancer Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs538334265	chr4:8026187-8026188	Enhancers Bivalent Enhancer Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs368448715	chr4:8026190-8026191	Enhancers Bivalent Enhancer Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs546496898	chr4:8026191-8026192	Enhancers Bivalent Enhancer Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs558436951	chr4:8026202-8026203	Enhancers Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs573347046	chr4:8026203-8026204	Enhancers Weak transcription Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs549133067	chr4:8026225-8026226	Enhancers Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs11726230	chr4:8026238-8026239	Enhancers Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs574444199	chr4:8026273-8026274	Enhancers Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs541438954	chr4:8026276-8026277	Enhancers Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs73092333	chr4:8026277-8026278	Enhancers Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs530743470	chr4:8026285-8026286	Enhancers Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs147515910	chr4:8026297-8026298	Enhancers Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs10049743	chr4:8026327-8026328	Enhancers Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs528284802	chr4:8026347-8026348	Enhancers Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs546728909	chr4:8026374-8026375	Enhancers Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs568483992	chr4:8026388-8026389	Enhancers Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs535919089	chr4:8026391-8026392	Enhancers Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs551021483	chr4:8026468-8026469	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs57679778	chr4:8026560-8026561	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs57322188	chr4:8026571-8026572	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs571505764	chr4:8026572-8026573	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs558177266	chr4:8026621-8026622	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs11726869	chr4:8026645-8026646	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs78400402	chr4:8026653-8026654	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs554413659	chr4:8026721-8026722	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs534148748	chr4:8026743-8026744	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs59720669	chr4:8026769-8026770	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs35314381	chr4:8026770-8026771	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs572391034	chr4:8026771-8026772	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs59413182	chr4:8026790-8026791	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs12502318	chr4:8026796-8026797	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs58453953	chr4:8026812-8026813	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs564062176	chr4:8026816-8026817	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs553061913	chr4:8026830-8026831	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs189776584	chr4:8026843-8026844	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs528359769	chr4:8026845-8026846	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs62290637	chr4:8026860-8026861	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs546495420	chr4:8026875-8026876	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs183419246	chr4:8026930-8026931	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs186328683	chr4:8026946-8026947	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs111613759	chr4:8026971-8026972	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs531370097	chr4:8026972-8026973	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs183485307	chr4:8026976-8026977	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs539842314	chr4:8026996-8026997	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs139486510	chr4:8027008-8027009	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs567065378	chr4:8027019-8027020	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs534489173	chr4:8027045-8027046	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs188532555	chr4:8027058-8027059	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs111834807	chr4:8027067-8027068	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
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
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:344 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8010600-8052000	Weak transcription	Left Ventricle	heart
2	chr4:8012400-8039000	Weak transcription	Gastric	stomach
3	chr4:8012800-8035000	Weak transcription	Pancreas	Pancrea
4	chr4:8013000-8036600	Weak transcription	Right Ventricle	heart
5	chr4:8014800-8031400	Strong transcription	Skeletal Muscle Female	skeletal muscle
6	chr4:8016400-8027400	Weak transcription	Aorta	Aorta
7	chr4:8017400-8040400	Weak transcription	Right Atrium	heart
8	chr4:8018800-8027200	Weak transcription	Psoas Muscle	Psoas
9	chr4:8020000-8031400	Strong transcription	Skeletal Muscle Male	skeletal muscle
10	chr4:8022000-8037600	Weak transcription	Lung	lung
11	chr4:8022200-8040600	Weak transcription	Fetal Brain Female	brain
12	chr4:8022400-8031000	Weak transcription	Esophagus	oesophagus
13	chr4:8022400-8035400	Weak transcription	Brain Anterior Caudate	brain
14	chr4:8022400-8039000	Weak transcription	Brain Angular Gyrus	brain
15	chr4:8023200-8039600	Weak transcription	Brain Germinal Matrix	brain
16	chr4:8023200-8041000	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr4:8023600-8029200	Weak transcription	Brain Hippocampus Middle	brain
18	chr4:8023800-8037200	Weak transcription	Brain Cingulate Gyrus	brain
19	chr4:8023800-8041200	Weak transcription	Brain Substantia Nigra	brain
20	chr4:8024000-8027400	Weak transcription	Spleen	Spleen
21	chr4:8025800-8026400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr4:8025800-8026400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
23	chr4:8025800-8026600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
24	chr4:8025800-8031800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr4:8026000-8026200	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr4:8026400-8031000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr4:8026600-8027600	Weak transcription	Stomach Smooth Muscle	stomach
28	chr4:8027200-8027800	Strong transcription	Psoas Muscle	Psoas
29	chr4:8027400-8027800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
30	chr4:8027400-8028800	Strong transcription	Spleen	Spleen
31	chr4:8027400-8030000	Strong transcription	Aorta	Aorta
32	chr4:8027600-8028200	Strong transcription	Stomach Smooth Muscle	stomach
33	chr4:8027800-8029000	Enhancers	Fetal Muscle Trunk	muscle
34	chr4:8027800-8029400	Enhancers	Fetal Muscle Leg	muscle
35	chr4:8027800-8030600	Weak transcription	Psoas Muscle	Psoas
36	chr4:8028000-8028200	Flanking Active TSS	HSMMtube	muscle
37	chr4:8028000-8028400	Enhancers	Placenta Amnion	Placenta Amnion
38	chr4:8028200-8028600	Weak transcription	Stomach Smooth Muscle	stomach
39	chr4:8028200-8029200	Enhancers	HSMMtube	muscle
40	chr4:8028400-8028800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr4:8028400-8029200	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr4:8028600-8028800	Enhancers	Stomach Smooth Muscle	stomach
43	chr4:8028600-8029400	Enhancers	HSMM	muscle
44	chr4:8028800-8029200	Genic enhancers	Spleen	Spleen
45	chr4:8028800-8035600	Weak transcription	Stomach Smooth Muscle	stomach
46	chr4:8029000-8029400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
47	chr4:8029200-8029800	Strong transcription	Brain Hippocampus Middle	brain
48	chr4:8029200-8031600	Weak transcription	HSMMtube	muscle
49	chr4:8029200-8031800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr4:8029200-8035400	Strong transcription	Spleen	Spleen

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