Variant report

Variant	esv1837218
Chromosome Location	chr5:177804032-177840382
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:140)
CpG islands
(count:977)
Chromatin interactive
region (count:16)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:140 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr5:177826063-177826418	K562	blood:	n/a	chr5:177826237-177826250
2	CEBPB	chr5:177838671-177838873	K562	blood:	n/a	chr5:177838715-177838726
3	CEBPB	chr5:177838609-177838848	HepG2	liver:	n/a	chr5:177838715-177838726
4	CEBPB	chr5:177820386-177820440	A549	lung:	n/a	n/a
5	CHD2	chr5:177807188-177807205	HepG2	liver:	n/a	n/a
6	CHD2	chr5:177811271-177811417	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr5:177818018-177818107	MCF-7	breast:	n/a	n/a
8	CTCF	chr5:177818069-177818101	LNCaP	prostate:	n/a	n/a
9	CTCF	chr5:177816400-177816550	SK-N-SH_RA	brain:	n/a	n/a
10	CTCF	chr5:177806840-177806990	GM12868	blood:	n/a	n/a
11	CTCF	chr5:177811999-177812127	H1-hESC	embryonic stem cell:	n/a	chr5:177812054-177812067 chr5:177812052-177812070 chr5:177812058-177812067
12	CTCF	chr5:177821214-177821253	Spleen_OC	spleen:	n/a	chr5:177821225-177821238
13	CTCF	chr5:177811920-177812070	GM06990	blood:	n/a	chr5:177812054-177812067 chr5:177812052-177812070 chr5:177812058-177812067
14	CTCF	chr5:177812020-177812170	HEK293	kidney:	n/a	chr5:177812054-177812067 chr5:177812052-177812070 chr5:177812058-177812067
15	CTCF	chr5:177812060-177812210	HL-60	blood:	n/a	n/a
16	CTCF	chr5:177824152-177824413	H1-hESC	embryonic stem cell:	n/a	chr5:177824310-177824326
17	CTCF	chr5:177818572-177818621	GM10266	blood:	n/a	n/a
18	CTCF	chr5:177812000-177812150	GM12864	blood:	n/a	chr5:177812054-177812067 chr5:177812052-177812070 chr5:177812058-177812067
19	CTCF	chr5:177838120-177838270	MCF-7	breast:	n/a	n/a
20	CTCF	chr5:177818429-177818472	LNCaP	prostate:	n/a	n/a
21	CTCF	chr5:177811980-177812130	WERI-Rb-1	eye:	n/a	chr5:177812054-177812067 chr5:177812052-177812070 chr5:177812058-177812067
22	CTCF	chr5:177818043-177818110	LNCaP	prostate:	n/a	n/a
23	CTCF	chr5:177824266-177824353	Medullo	brain:	n/a	chr5:177824310-177824326
24	CTCF	chr5:177807080-177807230	GM12868	blood:	n/a	n/a
25	CTCF	chr5:177811980-177812130	SK-N-SH_RA	brain:	n/a	chr5:177812054-177812067 chr5:177812052-177812070 chr5:177812058-177812067
26	CTCF	chr5:177824260-177824371	K562	blood:	n/a	chr5:177824310-177824326
27	CTCF	chr5:177824227-177824411	H1-hESC	embryonic stem cell:	n/a	chr5:177824310-177824326
28	CTCF	chr5:177818054-177818127	MCF-7	breast:	n/a	n/a
29	CTCF	chr5:177824220-177824370	WERI-Rb-1	eye:	n/a	chr5:177824310-177824326
30	CTCF	chr5:177818027-177818131	MCF-7	breast:	n/a	n/a
31	CTCF	chr5:177812020-177812170	GM12865	blood:	n/a	chr5:177812054-177812067 chr5:177812052-177812070 chr5:177812058-177812067
32	CTCF	chr5:177818040-177818101	MCF-7	breast:	n/a	n/a
33	E2F6	chr5:177811192-177811338	K562	blood:	n/a	n/a
34	EBF1	chr5:177808953-177809280	GM12878	blood:	n/a	chr5:177809130-177809139 chr5:177809128-177809141
35	EP300	chr5:177816288-177816737	SK-N-SH_RA	brain:	n/a	n/a
36	EP300	chr5:177811282-177811289	K562	blood:	n/a	n/a
37	EP300	chr5:177815861-177817068	SK-N-SH	brain:	n/a	n/a
38	EP300	chr5:177816282-177816732	SK-N-SH_RA	brain:	n/a	n/a
39	FOS	chr5:177812577-177812805	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr5:177821252-177821472	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr5:177821252-177821454	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr5:177812536-177812827	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr5:177812559-177812809	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr5:177832123-177832440	MCF10A-Er-Src	breast:	n/a	chr5:177832260-177832268
45	FOXA1	chr5:177814572-177814803	HepG2	liver:	n/a	n/a
46	FOXA2	chr5:177826464-177826713	HepG2	liver:	n/a	n/a
47	FOXA2	chr5:177826299-177826705	A549	lung:	n/a	n/a
48	GABPA	chr5:177824010-177824442	H1-hESC	embryonic stem cell:	n/a	n/a
49	GTF2F1	chr5:177824423-177824598	H1-hESC	embryonic stem cell:	n/a	n/a
50	HNF4A	chr5:177814486-177814752	HepG2	liver:	n/a	chr5:177814674-177814686

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:177805003-177805053	HepG2	liver:	n/a
2	chr5:177805003-177805053	HepG2	liver:	n/a
3	chr5:177821799-177821849	PANC-1	pancreas:	n/a
4	chr5:177824353-177824403	Caco-2	colon:	n/a
5	chr5:177805003-177805053	H1-hESC	embryonic stem cell:	embryo
6	chr5:177811648-177811698	HNPCEpiC	eye:	n/a
7	chr5:177821799-177821849	Hela-S3	cervix:	n/a
8	chr5:177811349-177811399	SK-N-SH_RA	brain:	n/a
9	chr5:177811349-177811399	BJ	skin:	n/a
10	chr5:177827484-177827534	GM06990	blood:	n/a
11	chr5:177805003-177805053	NT2-D1	testis:	n/a
12	chr5:177827484-177827534	LNCaP	prostate:	n/a
13	chr5:177805003-177805053	AG04449	skin:	fetal
14	chr5:177821799-177821849	NH-A	brain:	n/a
15	chr5:177814702-177814752	AG10803	skin:	n/a
16	chr5:177824353-177824403	HL-60	blood:	n/a
17	chr5:177811198-177811248	NT2-D1	testis:	n/a
18	chr5:177811198-177811248	K562	blood:	n/a
19	chr5:177823856-177823906	HPAEpiC	pulmonary alveolar:	n/a
20	chr5:177811198-177811248	Caco-2	colon:	n/a
21	chr5:177825282-177825332	RPTEC	kidney:	n/a
22	chr5:177819485-177819535	RPTEC	kidney:	n/a
23	chr5:177814702-177814752	NH-A	brain:	n/a
24	chr5:177809164-177809214	LNCaP	prostate:	n/a
25	chr5:177811349-177811399	HPAEpiC	pulmonary alveolar:	n/a
26	chr5:177824353-177824403	HAEpiC	amniotic membrane:	n/a
27	chr5:177805003-177805053	A549	lung:	n/a
28	chr5:177823864-177823914	SK-N-SH_RA	brain:	n/a
29	chr5:177809164-177809214	HAEpiC	amniotic membrane:	n/a
30	chr5:177823856-177823906	HL-60	blood:	n/a
31	chr5:177827484-177827534	NB4	blood:	n/a
32	chr5:177821799-177821849	HRCEpiC	kidney:	n/a
33	chr5:177827484-177827534	A549	lung:	n/a
34	chr5:177811648-177811698	SK-N-SH_RA	brain:	n/a
35	chr5:177811349-177811399	NB4	blood:	n/a
36	chr5:177814702-177814752	HEK293	kidney:	embryo
37	chr5:177805003-177805053	NHBE	bronchial:	n/a
38	chr5:177819485-177819535	HNPCEpiC	eye:	n/a
39	chr5:177809164-177809214	HEEpiC	esophagus:	n/a
40	chr5:177810294-177810344	CMK	blood:	n/a
41	chr5:177809164-177809214	NHBE	bronchial:	n/a
42	chr5:177811349-177811399	HL-60	blood:	n/a
43	chr5:177811349-177811399	PFSK-1	brain:	n/a
44	chr5:177824353-177824403	NHBE	bronchial:	n/a
45	chr5:177821799-177821849	HRE	kidney:	n/a
46	chr5:177824403-177824453	NHBE	bronchial:	n/a
47	chr5:177814702-177814752	SK-N-SH_RA	brain:	n/a
48	chr5:177824403-177824453	HEEpiC	esophagus:	n/a
49	chr5:177824353-177824403	ProgFib	skin:	n/a
50	chr5:177827484-177827534	HRPEpiC	eye:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:177808919..177811059-chr5:177815128..177817359,2	K562	blood:
2	chr5:177804316..177806496-chr5:177806617..177809077,2	K562	blood:
3	chr5:177811102..177814167-chr5:177815792..177819406,4	K562	blood:
4	chr5:177811102..177814167-chr5:177815792..177819406,4	K562	blood:
5	chr5:177806047..177808844-chr5:177816962..177819431,2	K562	blood:
6	chr5:177816543..177819082-chr5:177820341..177823036,2	K562	blood:
7	chr5:177811102..177812638-chr5:177817501..177819406,2	K562	blood:
8	chr5:177804849..177806989-chr5:177807066..177809838,2	MCF-7	breast:
9	chr5:177808919..177811059-chr5:177815128..177817359,2	K562	blood:
10	chr5:177786537..177789455-chr5:177802501..177804616,2	K562	blood:
11	chr5:177838677..177840723-chr5:177850329..177853314,2	K562	blood:
12	chr5:177799370..177801920-chr5:177806975..177809019,2	MCF-7	breast:
13	chr5:177806047..177808844-chr5:177816962..177819431,2	K562	blood:
14	chr5:177811102..177812638-chr5:177817501..177819406,2	K562	blood:
15	chr5:177816543..177819082-chr5:177820341..177823036,2	K562	blood:
16	chr5:177793010..177795271-chr5:177803266..177804910,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HNRNPAB-6	chr5:177804925-177805219	NONHSAT105532

No data

Variant related genes	Relation type
RN7SL646P	TF binding region
RN7SL646P	CpG island
ENSG00000242341	chromatin interactions

Extended variants
information (count: 1717 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1717 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2973725	chr5:177804032-177804033	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs13172345	chr5:177804060-177804061	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs372590859	chr5:177804099-177804100	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs543701634	chr5:177804109-177804110	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs181030997	chr5:177804121-177804122	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs140823736	chr5:177804122-177804123	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs377246047	chr5:177804123-177804124	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs530441561	chr5:177804124-177804125	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs568836500	chr5:177804127-177804128	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs368728765	chr5:177804131-177804132	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs17081176	chr5:177804143-177804144	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs546259941	chr5:177804159-177804160	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs564482600	chr5:177804201-177804202	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs147888213	chr5:177804205-177804206	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs114931027	chr5:177804208-177804209	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs141832310	chr5:177804228-177804229	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs150070132	chr5:177804232-177804233	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs547069617	chr5:177804243-177804244	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs145414059	chr5:177804280-177804281	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs149183354	chr5:177804302-177804303	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs560737312	chr5:177804332-177804333	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs186019613	chr5:177804358-177804359	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs35302321	chr5:177804362-177804363	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs397884287	chr5:177804365-177804366	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs114193464	chr5:177804400-177804401	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs34142157	chr5:177804410-177804411	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs13188035	chr5:177804428-177804429	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs569285427	chr5:177804442-177804443	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs573732223	chr5:177804453-177804454	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs541265160	chr5:177804456-177804457	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs200570190	chr5:177804461-177804462	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs201626763	chr5:177804465-177804466	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs10079261	chr5:177804468-177804469	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs10079266	chr5:177804488-177804489	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs137914908	chr5:177804505-177804506	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs2910120	chr5:177804546-177804547	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs112340770	chr5:177804548-177804549	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs531747727	chr5:177804607-177804608	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs373340513	chr5:177804622-177804623	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs10079384	chr5:177804679-177804680	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs10073512	chr5:177804688-177804689	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs373803089	chr5:177804701-177804702	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs28488884	chr5:177804703-177804704	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs115630823	chr5:177804709-177804710	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs190933000	chr5:177804712-177804713	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs532832523	chr5:177804728-177804729	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs370619936	chr5:177804729-177804730	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs111906235	chr5:177804736-177804737	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs181941692	chr5:177804737-177804738	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs144602719	chr5:177804775-177804776	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:422 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177798600-177804800	Weak transcription	Gastric	stomach
2	chr5:177798800-177816400	Weak transcription	Right Atrium	heart
3	chr5:177799800-177805600	Weak transcription	Ovary	ovary
4	chr5:177801200-177805800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr5:177802400-177805800	Bivalent Enhancer	Fetal Stomach	stomach
6	chr5:177802600-177807800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr5:177803400-177804800	Enhancers	Spleen	Spleen
8	chr5:177803600-177804400	Enhancers	Fetal Lung	lung
9	chr5:177803600-177804400	Bivalent Enhancer	Fetal Muscle Leg	muscle
10	chr5:177803600-177804600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr5:177803600-177805000	Strong transcription	Thymus	Thymus
12	chr5:177803600-177806000	Enhancers	Placenta	Placenta
13	chr5:177803800-177804400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:177803800-177804400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr5:177803800-177804400	Enhancers	Fetal Thymus	thymus
16	chr5:177803800-177804600	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr5:177804000-177804200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr5:177804000-177804200	Enhancers	Right Ventricle	heart
19	chr5:177804000-177804400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
20	chr5:177804000-177805000	Weak transcription	Fetal Heart	heart
21	chr5:177804000-177805200	Weak transcription	Fetal Intestine Large	intestine
22	chr5:177804000-177808600	Weak transcription	Fetal Intestine Small	intestine
23	chr5:177804200-177804400	Enhancers	Fetal Kidney	kidney
24	chr5:177804200-177804600	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr5:177804400-177804600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr5:177804400-177804600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr5:177804400-177804800	Weak transcription	Fetal Thymus	thymus
28	chr5:177804400-177805000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr5:177804400-177805400	Weak transcription	Fetal Lung	lung
30	chr5:177804600-177804800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr5:177804600-177805000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr5:177804600-177805800	Weak transcription	Fetal Kidney	kidney
33	chr5:177804600-177809600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr5:177804800-177805000	Enhancers	Fetal Thymus	thymus
35	chr5:177804800-177805000	Enhancers	Gastric	stomach
36	chr5:177804800-177807600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr5:177804800-177812800	Weak transcription	Spleen	Spleen
38	chr5:177805000-177809200	Weak transcription	Fetal Thymus	thymus
39	chr5:177805000-177809600	Weak transcription	Thymus	Thymus
40	chr5:177805000-177814800	Weak transcription	Gastric	stomach
41	chr5:177805200-177806600	Enhancers	Fetal Intestine Large	intestine
42	chr5:177805400-177806000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
43	chr5:177805400-177806600	Enhancers	Fetal Lung	lung
44	chr5:177805600-177805800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
45	chr5:177805600-177805800	Enhancers	Ovary	ovary
46	chr5:177805800-177806000	Enhancers	Fetal Brain Female	brain
47	chr5:177805800-177806200	Enhancers	Fetal Kidney	kidney
48	chr5:177805800-177806400	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr5:177805800-177806600	Enhancers	Duodenum Smooth Muscle	Duodenum
50	chr5:177805800-177808000	Enhancers	Fetal Stomach	stomach

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