Variant report

Variant	nsv465745
Chromosome Location	chr8:99061992-99116201
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:712)
CpG islands
(count:918)
Chromatin interactive
region (count:61)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:99080630-99082026	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:99079297-99079428	HepG2	liver:	n/a	n/a
3	ATF1	chr8:99105435-99105836	K562	blood:	n/a	n/a
4	BACH1	chr8:99076370-99077230	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:99078531-99078631	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr8:99110340-99110543	GM12878	blood:	n/a	n/a
7	BATF	chr8:99110333-99110625	GM12878	blood:	n/a	n/a
8	BHLHE40	chr8:99097929-99098118	K562	blood:	n/a	n/a
9	BHLHE40	chr8:99083023-99083731	GM12878	blood:	n/a	n/a
10	BHLHE40	chr8:99080957-99081256	HepG2	liver:	n/a	n/a
11	BHLHE40	chr8:99062509-99062558	A549	lung:	n/a	n/a
12	BRCA1	chr8:99097780-99098091	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr8:99105466-99105865	K562	blood:	n/a	n/a
14	CCNT2	chr8:99097917-99098202	K562	blood:	n/a	n/a
15	CEBPB	chr8:99070895-99071256	IMR90	lung:	n/a	n/a
16	CEBPB	chr8:99070914-99071270	K562	blood:	n/a	n/a
17	CEBPB	chr8:99091470-99091516	K562	blood:	n/a	n/a
18	CEBPB	chr8:99091320-99091615	A549	lung:	n/a	chr8:99091454-99091465
19	CEBPB	chr8:99086288-99086337	K562	blood:	n/a	n/a
20	CEBPB	chr8:99078829-99079138	MCF-7	breast:	n/a	chr8:99078917-99078930
21	CEBPB	chr8:99104181-99104489	MCF-7	breast:	n/a	chr8:99104282-99104293
22	CEBPB	chr8:99083597-99083893	HepG2	liver:	n/a	chr8:99083762-99083773
23	CEBPB	chr8:99070939-99071247	K562	blood:	n/a	n/a
24	CEBPB	chr8:99070890-99071262	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr8:99104168-99104418	H1-hESC	embryonic stem cell:	n/a	chr8:99104282-99104293
26	CEBPB	chr8:99091323-99091573	IMR90	lung:	n/a	chr8:99091454-99091465
27	CEBPB	chr8:99091361-99091571	HepG2	liver:	n/a	chr8:99091454-99091465
28	CEBPB	chr8:99070824-99071313	MCF-7	breast:	n/a	n/a
29	CEBPB	chr8:99091319-99091638	HepG2	liver:	n/a	chr8:99091454-99091465
30	CEBPB	chr8:99082821-99082837	IMR90	lung:	n/a	n/a
31	CEBPB	chr8:99091299-99091682	HepG2	liver:	n/a	chr8:99091454-99091465
32	CEBPB	chr8:99080841-99081277	HepG2	liver:	n/a	n/a
33	CEBPB	chr8:99070929-99071198	K562	blood:	n/a	n/a
34	CEBPB	chr8:99091302-99091722	MCF-7	breast:	n/a	chr8:99091454-99091465
35	CEBPB	chr8:99091300-99091676	HepG2	liver:	n/a	chr8:99091454-99091465
36	CEBPB	chr8:99104139-99104413	K562	blood:	n/a	chr8:99104282-99104293
37	CEBPB	chr8:99070975-99071228	A549	lung:	n/a	n/a
38	CEBPB	chr8:99070812-99071402	HCT-116	colon:	n/a	n/a
39	CEBPB	chr8:99091320-99091571	H1-hESC	embryonic stem cell:	n/a	chr8:99091454-99091465
40	CEBPB	chr8:99108074-99108254	K562	blood:	n/a	chr8:99108156-99108169
41	CEBPB	chr8:99070946-99071123	HepG2	liver:	n/a	n/a
42	CEBPB	chr8:99071035-99071124	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr8:99070816-99071292	MCF-7	breast:	n/a	n/a
44	CEBPB	chr8:99104167-99104425	A549	lung:	n/a	chr8:99104282-99104293
45	CEBPB	chr8:99070831-99071275	A549	lung:	n/a	n/a
46	CEBPB	chr8:99070958-99071247	A549	lung:	n/a	n/a
47	CEBPB	chr8:99069055-99069306	HepG2	liver:	n/a	n/a
48	CEBPB	chr8:99070718-99071386	HCT-116	colon:	n/a	n/a
49	CEBPB	chr8:99104191-99104339	HepG2	liver:	n/a	chr8:99104282-99104293
50	CEBPB	chr8:99104137-99104449	IMR90	lung:	n/a	chr8:99104282-99104293

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:99076605-99076655	ovcar-3	ovarian:	n/a
2	chr8:99076605-99076655	SK-N-MC	brain:	n/a
3	chr8:99077038-99077088	HCM	heart:	n/a
4	chr8:99076605-99076655	ovcar-3	ovarian:	n/a
5	chr8:99076605-99076655	SK-N-MC	brain:	n/a
6	chr8:99077038-99077088	HCM	heart:	n/a
7	chr8:99080123-99080173	GM12891	blood:	n/a
8	chr8:99077038-99077088	LNCaP	prostate:	n/a
9	chr8:99076526-99076576	K562	blood:	n/a
10	chr8:99076526-99076576	HRCEpiC	kidney:	n/a
11	chr8:99076813-99076863	HRE	kidney:	n/a
12	chr8:99076813-99076863	SAEC	small airway:	n/a
13	chr8:99076526-99076576	Jurkat	blood:	n/a
14	chr8:99076531-99076581	PANC-1	pancreas:	n/a
15	chr8:99077038-99077088	AG09309	skin:	n/a
16	chr8:99080123-99080173	HL-60	blood:	n/a
17	chr8:99076837-99076887	SK-N-SH_RA	brain:	n/a
18	chr8:99077817-99077867	HCPEpiC	choroid plexus:	n/a
19	chr8:99077817-99077867	HRCEpiC	kidney:	n/a
20	chr8:99077817-99077867	HIPEpiC	eye:	n/a
21	chr8:99076813-99076863	PFSK-1	brain:	n/a
22	chr8:99105576-99105626	NH-A	brain:	n/a
23	chr8:99076314-99076364	MCF10A-Er-Src	breast:	n/a
24	chr8:99077038-99077088	HIPEpiC	eye:	n/a
25	chr8:99076605-99076655	MCF-7	breast:	n/a
26	chr8:99076813-99076863	AG10803	skin:	n/a
27	chr8:99076531-99076581	MCF-7	breast:	n/a
28	chr8:99077038-99077088	NHBE	bronchial:	n/a
29	chr8:99076837-99076887	HEK293	kidney:	embryo
30	chr8:99105576-99105626	PANC-1	pancreas:	n/a
31	chr8:99076813-99076863	HCPEpiC	choroid plexus:	n/a
32	chr8:99105576-99105626	HUVEC	blood vessel:	n/a
33	chr8:99076837-99076887	K562	blood:	n/a
34	chr8:99076526-99076576	GM06990	blood:	n/a
35	chr8:99064617-99064667	HNPCEpiC	eye:	n/a
36	chr8:99076531-99076581	GM06990	blood:	n/a
37	chr8:99105576-99105626	SKMC	muscle:	n/a
38	chr8:99076837-99076887	U87	brain:	n/a
39	chr8:99076605-99076655	HRE	kidney:	n/a
40	chr8:99064617-99064667	AG10803	skin:	n/a
41	chr8:99080123-99080173	MCF-7	breast:	n/a
42	chr8:99077038-99077088	GM12892	blood:	n/a
43	chr8:99076314-99076364	ECC-1	luminal epithelium:	n/a
44	chr8:99076314-99076364	AG10803	skin:	n/a
45	chr8:99077132-99077182	NHDF-neo	bronchial:	n/a
46	chr8:99076837-99076887	HAEpiC	amniotic membrane:	n/a
47	chr8:99076734-99076784	HCF	heart:	n/a
48	chr8:99077038-99077088	MCF-7	breast:	n/a
49	chr8:99076837-99076887	Hepatocyte	liver:	n/a
50	chr8:99076837-99076887	BE2_C	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:99104954..99107804-chr8:99110176..99112228,2	K562	blood:
2	chr8:99101375..99102935-chr8:99104912..99106463,2	K562	blood:
3	chr8:99091170..99093628-chr8:99095565..99098052,2	K562	blood:
4	chr8:99049576..99051281-chr8:99112123..99114388,2	K562	blood:
5	chr8:99098046..99101467-chr8:99126201..99130139,4	MCF-7	breast:
6	chr8:99071093..99073717-chr8:99076624..99078418,2	MCF-7	breast:
7	chr8:99094554..99097746-chr8:99103141..99106033,3	MCF-7	breast:
8	chr8:99098084..99100230-chr8:99100397..99102063,2	K562	blood:
9	chr8:99100601..99102222-chr8:99121756..99123505,2	MCF-7	breast:
10	chr8:99056634..99059248-chr8:99059651..99063296,8	MCF-7	breast:
11	chr8:99110553..99112743-chr8:99124112..99126443,2	MCF-7	breast:
12	chr8:99114206..99122182-chr8:99125725..99131082,14	MCF-7	breast:
13	chr8:99058630..99060915-chr8:99087639..99090320,3	MCF-7	breast:
14	chr8:99056345..99058707-chr8:99104848..99107524,2	MCF-7	breast:
15	chr8:99046565..99048917-chr8:99089595..99092065,2	MCF-7	breast:
16	chr8:99114180..99116016-chr8:99124047..99126036,2	MCF-7	breast:
17	chr8:99056857..99059460-chr8:99091199..99095335,6	MCF-7	breast:
18	chr8:99099348..99102205-chr8:99104741..99107203,2	MCF-7	breast:
19	chr8:99114868..99117757-chr8:99127759..99130747,2	MCF-7	breast:
20	chr8:99080196..99082258-chr8:99098003..99099525,2	MCF-7	breast:
21	chr8:99056168..99061839-chr8:99079286..99085129,10	MCF-7	breast:
22	chr8:99085933..99088914-chr8:99090507..99092647,3	MCF-7	breast:
23	chr8:99056343..99058702-chr8:99077438..99079995,2	MCF-7	breast:
24	chr8:99085933..99088914-chr8:99090507..99092647,3	MCF-7	breast:
25	chr8:99055741..99058101-chr8:99104592..99107014,2	MCF-7	breast:
26	chr8:99099348..99102205-chr8:99104741..99107203,2	MCF-7	breast:
27	chr8:99080196..99082258-chr8:99098003..99099525,2	MCF-7	breast:
28	chr8:99094554..99097746-chr8:99103141..99106033,3	MCF-7	breast:
29	chr8:99057383..99059757-chr8:99103855..99106490,2	K562	blood:
30	chr8:99111083..99113381-chr8:99127604..99129611,2	MCF-7	breast:
31	chr8:99084386..99086516-chr8:99128038..99129656,2	MCF-7	breast:
32	chr8:99055453..99057832-chr8:99099813..99102793,3	MCF-7	breast:
33	chr8:99051546..99054747-chr8:99096963..99099980,5	MCF-7	breast:
34	chr8:99105894..99107758-chr8:99108714..99111067,2	MCF-7	breast:
35	chr8:99057312..99059712-chr8:99064427..99067887,3	K562	blood:
36	chr8:99049137..99049962-chr8:99097475..99098130,3	MCF-7	breast:
37	chr8:99056253..99058055-chr8:99098038..99100996,2	K562	blood:
38	chr8:99050817..99053848-chr8:99067344..99069783,4	K562	blood:
39	chr8:99056917..99058584-chr8:99095819..99097940,2	K562	blood:
40	chr8:99056304..99058591-chr8:99087479..99089177,4	MCF-7	breast:
41	chr8:99076443..99079804-chr8:99082104..99085952,3	K562	blood:
42	chr8:98879599..98882619-chr8:99058852..99062253,4	MCF-7	breast:
43	chr8:99056304..99059597-chr8:99060333..99064411,5	K562	blood:
44	chr8:99104954..99107804-chr8:99110176..99112228,2	K562	blood:
45	chr8:99048693..99052223-chr8:99096382..99099450,4	MCF-7	breast:
46	chr8:99053215..99055370-chr8:99061297..99063461,2	K562	blood:
47	chr8:99098084..99100230-chr8:99100397..99102063,2	K562	blood:
48	chr8:99057798..99060309-chr8:99094046..99095813,2	MCF-7	breast:
49	chr8:99056928..99058682-chr8:99096688..99098229,2	MCF-7	breast:
50	chr8:98879754..98881586-chr8:99098019..99100766,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf47-1	chr8:99111578-99112805	NONHSAT127909

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	HRSP12	hsa-miR-375	chr8:99114622-99114643

Variant related genes	Relation type
C8orf47	TF binding region
RPL30	TF binding region
C8orf47	CpG island
RPL30	CpG island
ENSG00000104356	chromatin interactions
ENSG00000156482	chromatin interactions
ENSG00000132541	chromatin interactions
ENSG00000132561	chromatin interactions
ENSG00000245970	chromatin interactions
ENSG00000207067	chromatin interactions
ENSG00000252755	chromatin interactions
ENSG00000177459	chromatin interactions

Extended variants
information (count: 2110 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:2110 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12545793	chr8:99061992-99061993	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561602005	chr8:99062034-99062035	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs189179257	chr8:99062070-99062071	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs542528120	chr8:99062089-99062090	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs571048512	chr8:99062096-99062097	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs550291599	chr8:99062125-99062126	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs570153954	chr8:99062126-99062127	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs113696301	chr8:99062131-99062132	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs148490865	chr8:99062175-99062176	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs533316721	chr8:99062226-99062227	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs564002768	chr8:99062265-99062266	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs530513433	chr8:99062292-99062293	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs546443273	chr8:99062304-99062305	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs566437448	chr8:99062311-99062312	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs552188542	chr8:99062359-99062360	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs71570285	chr8:99062388-99062389	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs13281514	chr8:99062391-99062392	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs13279885	chr8:99062392-99062393	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs555556642	chr8:99062449-99062450	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs2444857	chr8:99062480-99062481	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs537583829	chr8:99062492-99062493	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs376785957	chr8:99062606-99062607	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs181876256	chr8:99062614-99062615	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs557380068	chr8:99062658-99062659	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs577265345	chr8:99062671-99062672	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs13280033	chr8:99062693-99062694	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs13280054	chr8:99062711-99062712	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs370944078	chr8:99062714-99062715	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs13280288	chr8:99062727-99062728	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs149432625	chr8:99062774-99062775	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs79777911	chr8:99062864-99062865	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs76065021	chr8:99062886-99062887	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs145240931	chr8:99062918-99062919	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs562342339	chr8:99062938-99062939	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs530513964	chr8:99062991-99062992	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs544340540	chr8:99063079-99063080	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs554186323	chr8:99063170-99063171	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs563840027	chr8:99063272-99063273	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs371525413	chr8:99063275-99063276	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs546203332	chr8:99063330-99063331	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs566398614	chr8:99063339-99063340	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs11995769	chr8:99063340-99063341	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs548888037	chr8:99063342-99063343	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs567949551	chr8:99063355-99063356	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs537650487	chr8:99063357-99063358	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs557452768	chr8:99063391-99063392	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs183988039	chr8:99063450-99063451	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs570975704	chr8:99063463-99063464	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs186478356	chr8:99063477-99063478	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs374622297	chr8:99063492-99063493	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Malignant melanoma	17260012	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Prostate cancer	22341455	CNVD
Colorectal cancer	19455253	CNVD

Chromatin state (count:664 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:99059000-99063400	Weak transcription	Brain Angular Gyrus	brain
2	chr8:99059200-99062000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr8:99059200-99062000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr8:99059200-99062000	Weak transcription	Right Ventricle	heart
5	chr8:99059200-99062000	Weak transcription	HSMM	muscle
6	chr8:99059200-99062200	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr8:99059200-99062400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr8:99059200-99062600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr8:99059200-99062800	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr8:99059200-99063000	Weak transcription	GM12878-XiMat	blood
11	chr8:99059200-99063200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr8:99059200-99063200	Weak transcription	Fetal Kidney	kidney
13	chr8:99059200-99063400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr8:99059200-99063400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr8:99059200-99064000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr8:99059200-99064200	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr8:99059200-99065000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr8:99059200-99066200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr8:99059200-99070800	Weak transcription	A549	lung
20	chr8:99059200-99071000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr8:99059400-99062000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr8:99059400-99062000	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr8:99059400-99062200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr8:99059400-99062800	Weak transcription	Pancreas	Pancrea
25	chr8:99059400-99063200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr8:99059400-99063200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr8:99059400-99063600	Weak transcription	Fetal Intestine Large	intestine
28	chr8:99059400-99063600	Weak transcription	Fetal Muscle Trunk	muscle
29	chr8:99059400-99064600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr8:99059400-99076200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr8:99059600-99064400	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr8:99060000-99064200	Weak transcription	Fetal Intestine Small	intestine
33	chr8:99060800-99064600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr8:99060800-99065000	Weak transcription	Liver	Liver
35	chr8:99061200-99063000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr8:99061400-99062800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr8:99061800-99062000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr8:99061800-99062200	Enhancers	NHDF-Ad	bronchial
39	chr8:99061800-99062200	Enhancers	Osteobl	bone
40	chr8:99062000-99062200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr8:99062000-99062400	Enhancers	HSMM	muscle
42	chr8:99062000-99062600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr8:99062200-99062600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr8:99064600-99064800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr8:99064800-99076400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr8:99066200-99067000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr8:99068400-99070200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr8:99068600-99069800	Enhancers	HepG2	liver
49	chr8:99068800-99069200	Enhancers	Ovary	ovary
50	chr8:99069200-99076200	Weak transcription	Ovary	ovary

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