Variant report

Variant	nsv537154
Chromosome Location	chr4:81480374-81802614
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1080)
CpG islands
(count:61)
Chromatin interactive
region (count:37)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1080 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:81540281-81540488	K562	blood:	n/a	n/a
2	ARID3A	chr4:81536315-81536564	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:81540306-81540462	HepG2	liver:	n/a	n/a
4	ATF2	chr4:81796747-81797219	GM12878	blood:	n/a	n/a
5	ATF2	chr4:81797888-81798408	GM12878	blood:	n/a	n/a
6	ATF2	chr4:81763026-81763419	GM12878	blood:	n/a	n/a
7	ATF2	chr4:81796730-81797216	GM12878	blood:	n/a	n/a
8	ATF2	chr4:81797799-81798459	GM12878	blood:	n/a	n/a
9	BACH1	chr4:81631922-81632282	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:81672435-81672720	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr4:81797909-81798372	GM12878	blood:	n/a	n/a
12	BATF	chr4:81796744-81797221	GM12878	blood:	n/a	n/a
13	BATF	chr4:81763070-81763363	GM12878	blood:	n/a	n/a
14	BATF	chr4:81711363-81711557	GM12878	blood:	n/a	chr4:81711432-81711440
15	BATF	chr4:81797914-81798369	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:81532008-81532366	GM12878	blood:	n/a	n/a
17	BCL11A	chr4:81797973-81798345	GM12878	blood:	n/a	chr4:81798148-81798157
18	BCL11A	chr4:81763125-81763395	GM12878	blood:	n/a	n/a
19	BCL11A	chr4:81797887-81798401	GM12878	blood:	n/a	chr4:81798148-81798157
20	BCL11A	chr4:81532131-81532308	GM12878	blood:	n/a	n/a
21	BCL11A	chr4:81796748-81797201	GM12878	blood:	n/a	n/a
22	BCL11A	chr4:81646559-81646736	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCL3	chr4:81797868-81798380	GM12878	blood:	n/a	chr4:81798148-81798157
24	BCL3	chr4:81797892-81798328	GM12878	blood:	n/a	chr4:81798148-81798157
25	BCLAF1	chr4:81796774-81797043	GM12878	blood:	n/a	n/a
26	BCLAF1	chr4:81797918-81798340	GM12878	blood:	n/a	chr4:81798148-81798157
27	BCLAF1	chr4:81796740-81797149	GM12878	blood:	n/a	n/a
28	BCLAF1	chr4:81797821-81798479	GM12878	blood:	n/a	chr4:81798148-81798157
29	BHLHE40	chr4:81796831-81797153	GM12878	blood:	n/a	n/a
30	BHLHE40	chr4:81533942-81534173	GM12878	blood:	n/a	n/a
31	BHLHE40	chr4:81798003-81798335	GM12878	blood:	n/a	n/a
32	BHLHE40	chr4:81531862-81532820	GM12878	blood:	n/a	n/a
33	BRCA1	chr4:81509298-81509310	GM12878	blood:	n/a	n/a
34	CCNT2	chr4:81569268-81569430	K562	blood:	n/a	n/a
35	CCNT2	chr4:81735997-81736139	K562	blood:	n/a	n/a
36	CEBPB	chr4:81799440-81799740	K562	blood:	n/a	chr4:81799582-81799593
37	CEBPB	chr4:81752924-81753282	IMR90	lung:	n/a	n/a
38	CEBPB	chr4:81534827-81535128	HepG2	liver:	n/a	chr4:81534961-81534972 chr4:81534959-81534970
39	CEBPB	chr4:81627116-81627294	K562	blood:	n/a	chr4:81627168-81627179 chr4:81627168-81627181 chr4:81627169-81627180 chr4:81627168-81627181
40	CEBPB	chr4:81536259-81536581	MCF-7	breast:	n/a	chr4:81536451-81536459
41	CEBPB	chr4:81796625-81797217	GM12878	blood:	n/a	n/a
42	CEBPB	chr4:81536325-81536607	HepG2	liver:	n/a	chr4:81536451-81536459
43	CEBPB	chr4:81649215-81649440	A549	lung:	n/a	chr4:81649334-81649347 chr4:81649334-81649345 chr4:81649336-81649347 chr4:81649336-81649345
44	CEBPB	chr4:81576458-81576621	IMR90	lung:	n/a	n/a
45	CEBPB	chr4:81763237-81763426	HepG2	liver:	n/a	chr4:81763334-81763345 chr4:81763333-81763346
46	CEBPB	chr4:81797837-81798442	GM12878	blood:	n/a	chr4:81798354-81798365 chr4:81798354-81798367 chr4:81798354-81798365
47	CEBPB	chr4:81649163-81649464	IMR90	lung:	n/a	chr4:81649334-81649347 chr4:81649334-81649345 chr4:81649336-81649347 chr4:81649336-81649345
48	CEBPB	chr4:81802404-81802765	HepG2	liver:	n/a	n/a
49	CEBPB	chr4:81562097-81562342	IMR90	lung:	n/a	chr4:81562115-81562126 chr4:81562231-81562242
50	CEBPB	chr4:81799431-81799764	HepG2	liver:	n/a	chr4:81799582-81799593

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:81660494-81660544	AG04450	lung:	fetal
2	chr4:81660494-81660544	BJ	skin:	n/a
3	chr4:81660494-81660544	MCF10A-Er-Src	breast:	n/a
4	chr4:81660494-81660544	HMEC	breast:	n/a
5	chr4:81660494-81660544	HEK293	kidney:	embryo
6	chr4:81660494-81660544	GM06990	blood:	n/a
7	chr4:81660494-81660544	HRE	kidney:	n/a
8	chr4:81660494-81660544	HUVEC	blood vessel:	n/a
9	chr4:81660494-81660544	PrEC	prostate:	n/a
10	chr4:81660494-81660544	GM12878	blood:	n/a
11	chr4:81660494-81660544	NT2-D1	testis:	n/a
12	chr4:81660494-81660544	HCM	heart:	n/a
13	chr4:81660494-81660544	SK-N-SH	brain:	n/a
14	chr4:81660494-81660544	NH-A	brain:	n/a
15	chr4:81660494-81660544	HCPEpiC	choroid plexus:	n/a
16	chr4:81660494-81660544	NHDF-neo	bronchial:	n/a
17	chr4:81660494-81660544	HRCEpiC	kidney:	n/a
18	chr4:81660494-81660544	SK-N-SH_RA	brain:	n/a
19	chr4:81660494-81660544	Caco-2	colon:	n/a
20	chr4:81660494-81660544	HPAEpiC	pulmonary alveolar:	n/a
21	chr4:81660494-81660544	HCF	heart:	n/a
22	chr4:81660494-81660544	AG09319	gingival:	n/a
23	chr4:81660494-81660544	K562	blood:	n/a
24	chr4:81660494-81660544	A549	lung:	n/a
25	chr4:81660494-81660544	SK-N-MC	brain:	n/a
26	chr4:81660494-81660544	GM19239	blood:	n/a
27	chr4:81660494-81660544	Hela-S3	cervix:	n/a
28	chr4:81660494-81660544	SAEC	small airway:	n/a
29	chr4:81660494-81660544	HepG2	liver:	n/a
30	chr4:81660494-81660544	HRPEpiC	eye:	n/a
31	chr4:81660494-81660544	NB4	blood:	n/a
32	chr4:81660494-81660544	T-47D	breast:	n/a
33	chr4:81660494-81660544	ovcar-3	ovarian:	n/a
34	chr4:81660494-81660544	ECC-1	luminal epithelium:	n/a
35	chr4:81660494-81660544	AG10803	skin:	n/a
36	chr4:81660494-81660544	AG09309	skin:	n/a
37	chr4:81660494-81660544	HCT-116	colon:	n/a
38	chr4:81660494-81660544	NHBE	bronchial:	n/a
39	chr4:81660494-81660544	H1-hESC	embryonic stem cell:	embryo
40	chr4:81660494-81660544	Jurkat	blood:	n/a
41	chr4:81660494-81660544	AoSMC	blood vessel:	n/a
42	chr4:81660494-81660544	RPTEC	kidney:	n/a
43	chr4:81660494-81660544	SKMC	muscle:	n/a
44	chr4:81660494-81660544	HIPEpiC	eye:	n/a
45	chr4:81660494-81660544	GM12891	blood:	n/a
46	chr4:81660494-81660544	ProgFib	skin:	n/a
47	chr4:81660494-81660544	CMK	blood:	n/a
48	chr4:81660494-81660544	GM12892	blood:	n/a
49	chr4:81660494-81660544	HEEpiC	esophagus:	n/a
50	chr4:81660494-81660544	PFSK-1	brain:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:81489877..81492717-chr4:81494279..81495891,2	K562	blood:
2	chr4:81675024..81677114-chr4:81678812..81680494,2	K562	blood:
3	chr4:81540203..81541132-chr4:81973708..81974534,2	MCF-7	breast:
4	chr4:81652068..81654710-chr4:81662005..81664580,2	MCF-7	breast:
5	chr4:81794667..81796938-chr4:81800579..81802304,2	K562	blood:
6	chr4:81543453..81546267-chr4:81555168..81557103,2	MCF-7	breast:
7	chr4:81581396..81581979-chr4:81761045..81761732,2	MCF-7	breast:
8	chr4:81581396..81581979-chr4:81761045..81761732,2	MCF-7	breast:
9	chr4:81499228..81501687-chr4:81505021..81507173,2	K562	blood:
10	chr4:81627156..81628838-chr4:81631785..81634489,2	K562	blood:
11	chr4:81627156..81628838-chr4:81631785..81634489,2	K562	blood:
12	chr4:81756515..81759052-chr4:81760734..81762863,2	K562	blood:
13	chr4:81486208..81487933-chr4:81500927..81502953,2	K562	blood:
14	chr4:81652068..81654710-chr4:81662005..81664580,2	MCF-7	breast:
15	chr4:81667228..81669578-chr4:81671291..81673387,2	MCF-7	breast:
16	chr4:81519146..81521026-chr4:81528690..81531037,2	MCF-7	breast:
17	chr4:81696073..81698276-chr4:81701029..81703703,2	K562	blood:
18	chr4:81519146..81521026-chr4:81528690..81531037,2	MCF-7	breast:
19	chr4:81486208..81487933-chr4:81500927..81502953,2	K562	blood:
20	chr4:81732367..81734767-chr4:81734914..81738399,4	K562	blood:
21	chr4:81794667..81796938-chr4:81800579..81802304,2	K562	blood:
22	chr4:81624160..81627209-chr4:81627794..81630276,3	K562	blood:
23	chr4:81667228..81669578-chr4:81671291..81673387,2	MCF-7	breast:
24	chr4:81489877..81492717-chr4:81494279..81495891,2	K562	blood:
25	chr4:81789838..81792795-chr4:81793181..81795732,2	MCF-7	breast:
26	chr4:81726557..81729431-chr4:81734231..81736856,2	MCF-7	breast:
27	chr4:81286836..81287415-chr4:81540565..81541217,2	MCF-7	breast:
28	chr4:81539992..81540886-chr4:81910834..81911713,5	MCF-7	breast:
29	chr4:81726557..81729431-chr4:81734231..81736856,2	MCF-7	breast:
30	chr20:5429160..5429789-chr4:81671748..81672503,2	MCF-7	breast:
31	chr4:81543453..81546267-chr4:81555168..81557103,2	MCF-7	breast:
32	chr4:81732367..81734767-chr4:81734914..81738399,4	K562	blood:
33	chr4:81756515..81759052-chr4:81760734..81762863,2	K562	blood:
34	chr4:81696073..81698276-chr4:81701029..81703703,2	K562	blood:
35	chr4:81624160..81627209-chr4:81627794..81630276,3	K562	blood:
36	chr4:81675024..81677114-chr4:81678812..81680494,2	K562	blood:
37	chr4:81499228..81501687-chr4:81505021..81507173,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BMP3-2	chr4:81791203-81791289	NONHSAT097143

No data

Variant related genes	Relation type
C4orf22	TF binding region
C4orf22	CpG island
ENSG00000197826	chromatin interactions

Extended variants
information (count: 4451 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4451 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376320349	chr4:81487257-81487258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs554331401	chr4:81487324-81487325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574297453	chr4:81487401-81487402	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188834436	chr4:81487428-81487429	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs567447032	chr4:81487430-81487431	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs145120439	chr4:81487459-81487460	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs34710831	chr4:81487463-81487464	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181201541	chr4:81487470-81487471	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573294264	chr4:81487513-81487514	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs545365075	chr4:81487516-81487517	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs368532100	chr4:81487565-81487566	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs531224626	chr4:81487568-81487569	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs202098506	chr4:81487617-81487618	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs74490502	chr4:81487618-81487619	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs139962745	chr4:81487630-81487631	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs73832422	chr4:81487631-81487632	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs372576215	chr4:81487632-81487633	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs530337808	chr4:81487634-81487635	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs143445348	chr4:81487659-81487660	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs17004942	chr4:81487729-81487730	Active TSS Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs146731569	chr4:81487757-81487758	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs552889151	chr4:81487806-81487807	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs140314835	chr4:81487816-81487817	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs142566655	chr4:81487829-81487830	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs563092585	chr4:81487905-81487906	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs150957329	chr4:81487995-81487996	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs537705789	chr4:81488019-81488020	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs554466213	chr4:81488052-81488053	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs531783212	chr4:81488056-81488057	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs10857174	chr4:81488139-81488140	Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs533974125	chr4:81488150-81488151	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs139864901	chr4:81488152-81488153	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs199558331	chr4:81488169-81488170	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs553712084	chr4:81488179-81488180	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs573287255	chr4:81488189-81488190	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs376742681	chr4:81488220-81488221	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs140739280	chr4:81488250-81488251	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs7690311	chr4:81488340-81488341	Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs575714418	chr4:81488377-81488378	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs7666589	chr4:81488421-81488422	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs7695414	chr4:81488436-81488437	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs570089997	chr4:81488492-81488493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114857105	chr4:81488507-81488508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs17004943	chr4:81488510-81488511	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs150084177	chr4:81488564-81488565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543830609	chr4:81488619-81488620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138621759	chr4:81488635-81488636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373121431	chr4:81488658-81488659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552609168	chr4:81488691-81488692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141882003	chr4:81488766-81488767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Myelodysplastic syndrome	18508791	CNVD
abnormal development	18461090	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Chronic lymphocytic leukemia	21215367	CNVD
Cancer	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:81487200-81487600	Enhancers	Osteobl	bone
2	chr4:81487400-81487600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr4:81487400-81488400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr4:81487600-81487800	Flanking Active TSS	Osteobl	bone
5	chr4:81487600-81488000	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr4:81487600-81488000	Active TSS	Fetal Intestine Small	intestine
7	chr4:81487600-81488200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr4:81487600-81488200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr4:81487600-81488200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr4:81487600-81488200	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr4:81487600-81488200	Active TSS	Stomach Smooth Muscle	stomach
12	chr4:81487600-81488200	Active TSS	HMEC	breast
13	chr4:81487600-81488400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr4:81487600-81488400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr4:81487600-81488400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr4:81487600-81488400	Active TSS	Duodenum Mucosa	Duodenum
17	chr4:81487600-81488400	Active TSS	Ovary	ovary
18	chr4:81487800-81488200	Active TSS	Duodenum Smooth Muscle	Duodenum
19	chr4:81487800-81488200	Active TSS	Rectal Mucosa Donor 29	rectum
20	chr4:81487800-81488200	Active TSS	Rectal Smooth Muscle	rectum
21	chr4:81487800-81488200	Active TSS	NHDF-Ad	bronchial
22	chr4:81487800-81488400	Active TSS	Osteobl	bone
23	chr4:81488200-81488400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr4:81488400-81494800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr4:81489800-81490200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr4:81490000-81490400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr4:81490000-81490400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:81490000-81490400	Enhancers	Gastric	stomach
29	chr4:81494800-81495000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr4:81499000-81501000	Enhancers	Fetal Kidney	kidney
31	chr4:81501000-81501200	Weak transcription	Fetal Kidney	kidney
32	chr4:81501200-81502200	Enhancers	Fetal Kidney	kidney
33	chr4:81501400-81502000	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr4:81501400-81502000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr4:81501400-81502200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr4:81501400-81502400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr4:81501400-81502600	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr4:81501400-81504000	Enhancers	Primary T cells from cord blood	blood
39	chr4:81501600-81502400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr4:81501600-81502600	Enhancers	Primary hematopoietic stem cells	blood
41	chr4:81501600-81502600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
42	chr4:81501800-81502200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr4:81501800-81502200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr4:81501800-81502600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
45	chr4:81502200-81503400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr4:81502200-81503800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr4:81502200-81508000	Weak transcription	Fetal Kidney	kidney
48	chr4:81502200-81509000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr4:81502600-81503000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr4:81502600-81503000	Weak transcription	Primary T helper cells PMA-I stimulated	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links