Variant report

Variant	nsv893432
Chromosome Location	chr9:72028323-72056397
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:72037187-72037443	HepG2	liver:	n/a	n/a
2	BACH1	chr9:72044969-72045003	H1-hESC	embryonic stem cell:	n/a	n/a
3	CBX3	chr9:72046604-72047163	K562	blood:	n/a	n/a
4	CBX3	chr9:72046628-72046987	K562	blood:	n/a	n/a
5	CEBPB	chr9:72037167-72037438	Hela-S3	cervix:	n/a	n/a
6	CEBPD	chr9:72046517-72047194	K562	blood:	n/a	n/a
7	CEBPD	chr9:72046554-72047083	K562	blood:	n/a	n/a
8	CHD2	chr9:72036898-72036903	GM12878	blood:	n/a	n/a
9	CTCF	chr9:72037220-72037370	HMF	breast:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
10	CTCF	chr9:72036923-72037694	HCT-116	colon:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
11	CTCF	chr9:72040380-72040530	MCF-7	breast:	n/a	n/a
12	CTCF	chr9:72037200-72037350	NHDF-neo	bronchial:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
13	CTCF	chr9:72036933-72037087	GM19238	blood:	n/a	n/a
14	CTCF	chr9:72037180-72037330	WERI-Rb-1	eye:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
15	CTCF	chr9:72036560-72036710	RPTEC	kidney:	n/a	n/a
16	CTCF	chr9:72037149-72037420	Pancreas_OC	pancreas:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
17	CTCF	chr9:72037149-72037412	GM10266	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
18	CTCF	chr9:72037063-72037490	K562	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
19	CTCF	chr9:72037121-72037431	GM12878	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
20	CTCF	chr9:72043377-72043603	K562	blood:	n/a	n/a
21	CTCF	chr9:72037206-72037394	MCF-7	breast:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
22	CTCF	chr9:72043408-72043530	K562	blood:	n/a	n/a
23	CTCF	chr9:72040239-72040740	MCF-7	breast:	n/a	n/a
24	CTCF	chr9:72037200-72037350	HAc	cerebellar:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
25	CTCF	chr9:72037200-72037350	GM12874	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
26	CTCF	chr9:72037220-72037370	HVMF	connective:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
27	CTCF	chr9:72037086-72037384	A549	lung:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
28	CTCF	chr9:72037200-72037350	WERI-Rb-1	eye:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
29	CTCF	chr9:72037220-72037370	BJ	skin:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
30	CTCF	chr9:72037180-72037330	GM12868	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
31	CTCF	chr9:72037180-72037330	HAc	cerebellar:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
32	CTCF	chr9:72037094-72037562	K562	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
33	CTCF	chr9:72037079-72037535	IMR90	lung:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
34	CTCF	chr9:72037075-72037596	MCF-7	breast:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
35	CTCF	chr9:72037220-72037370	HRE	kidney:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
36	CTCF	chr9:72037200-72037350	HCT-116	colon:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
37	CTCF	chr9:72037180-72037330	HCM	heart:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
38	CTCF	chr9:72037494-72037512	GM12891	blood:	n/a	n/a
39	CTCF	chr9:72036840-72036990	GM12872	blood:	n/a	n/a
40	CTCF	chr9:72037240-72037390	GM12870	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
41	CTCF	chr9:72037200-72037350	HEEpiC	esophagus:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
42	CTCF	chr9:72037180-72037330	GM12865	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
43	CTCF	chr9:72043426-72043504	A549	lung:	n/a	n/a
44	CTCF	chr9:72040361-72040584	MCF-7	breast:	n/a	n/a
45	CTCF	chr9:72037180-72037458	GM19239	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
46	CTCF	chr9:72043360-72043510	K562	blood:	n/a	n/a
47	CTCF	chr9:72036820-72036970	HCM	heart:	n/a	n/a
48	CTCF	chr9:72037200-72037350	HepG2	liver:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
49	CTCF	chr9:72037220-72037370	HCFaa	heart:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
50	CTCF	chr9:72036915-72037448	GM12891	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:72046240-72046290	NHBE	bronchial:	n/a
2	chr9:72046240-72046290	Jurkat	blood:	n/a
3	chr9:72046240-72046290	HPAEpiC	pulmonary alveolar:	n/a
4	chr9:72046240-72046290	HNPCEpiC	eye:	n/a
5	chr9:72046240-72046290	AG09309	skin:	n/a
6	chr9:72046240-72046290	NT2-D1	testis:	n/a
7	chr9:72046240-72046290	SAEC	small airway:	n/a
8	chr9:72046240-72046290	BE2_C	brain:	n/a
9	chr9:72046240-72046290	HIPEpiC	eye:	n/a
10	chr9:72046240-72046290	HCPEpiC	choroid plexus:	n/a
11	chr9:72046240-72046290	PFSK-1	brain:	n/a
12	chr9:72046240-72046290	HAEpiC	amniotic membrane:	n/a
13	chr9:72046240-72046290	HEK293	kidney:	embryo
14	chr9:72046240-72046290	NB4	blood:	n/a
15	chr9:72046240-72046290	AoSMC	blood vessel:	n/a
16	chr9:72046240-72046290	Hepatocyte	liver:	n/a
17	chr9:72046240-72046290	Caco-2	colon:	n/a
18	chr9:72046240-72046290	GM06990	blood:	n/a
19	chr9:72046240-72046290	PANC-1	pancreas:	n/a
20	chr9:72046240-72046290	HMEC	breast:	n/a
21	chr9:72046240-72046290	SK-N-SH	brain:	n/a
22	chr9:72046240-72046290	U87	brain:	n/a
23	chr9:72046240-72046290	GM12878	blood:	n/a
24	chr9:72046240-72046290	A549	lung:	n/a
25	chr9:72046240-72046290	IMR90	lung:	fetal
26	chr9:72046240-72046290	PrEC	prostate:	n/a
27	chr9:72046240-72046290	MCF-7	breast:	n/a
28	chr9:72046240-72046290	GM12891	blood:	n/a
29	chr9:72046240-72046290	RPTEC	kidney:	n/a
30	chr9:72046240-72046290	BJ	skin:	n/a
31	chr9:72046240-72046290	MCF10A-Er-Src	breast:	n/a
32	chr9:72046240-72046290	HEEpiC	esophagus:	n/a
33	chr9:72046240-72046290	CMK	blood:	n/a
34	chr9:72046240-72046290	ProgFib	skin:	n/a
35	chr9:72046240-72046290	HRE	kidney:	n/a
36	chr9:72046240-72046290	HCF	heart:	n/a
37	chr9:72046240-72046290	GM19239	blood:	n/a
38	chr9:72046240-72046290	K562	blood:	n/a
39	chr9:72046240-72046290	HepG2	liver:	n/a
40	chr9:72046240-72046290	GM12892	blood:	n/a
41	chr9:72046240-72046290	HCM	heart:	n/a
42	chr9:72046240-72046290	ovcar-3	ovarian:	n/a
43	chr9:72046240-72046290	AG04449	skin:	fetal
44	chr9:72046240-72046290	ECC-1	luminal epithelium:	n/a
45	chr9:72046240-72046290	SK-N-SH_RA	brain:	n/a
46	chr9:72046240-72046290	H1-hESC	embryonic stem cell:	embryo
47	chr9:72046240-72046290	HL-60	blood:	n/a
48	chr9:72046240-72046290	AG10803	skin:	n/a
49	chr9:72046240-72046290	HUVEC	blood vessel:	n/a
50	chr9:72046240-72046290	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:72036812..72037787-chr9:72160880..72161856,6	MCF-7	breast:
2	chr9:72044312..72045985-chr9:72046714..72048470,2	MCF-7	breast:
3	chr9:72036807..72037778-chr9:72056686..72057333,2	MCF-7	breast:
4	chr9:72039845..72040903-chr9:72160889..72161458,4	MCF-7	breast:
5	chr9:72044312..72045985-chr9:72046714..72048470,2	MCF-7	breast:
6	chr9:72036895..72038079-chr9:72163773..72164881,7	MCF-7	breast:
7	chr9:72036664..72037777-chr9:72163377..72165001,9	K562	blood:
8	chr9:72038579..72040872-chr9:72161729..72164338,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-APBA1-1	chr9:72043164-72043467	ENSG00000243888
2	lnc-APBA1-1	chr9:72042449-72044751	NONHSAT131778
3	lnc-APBA1-1	chr9:72043544-72043637	ENSG00000243888

Variant related genes	Relation type
ENSG00000243888	TF binding region
ENSG00000243888	CpG island

Extended variants
information (count: 1151 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1151 , 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	rs2777860	chr9:72028323-72028324	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561786699	chr9:72028356-72028357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528973030	chr9:72028382-72028383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190823649	chr9:72028500-72028501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs568759501	chr9:72028514-72028515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539373918	chr9:72028538-72028539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs28483200	chr9:72028608-72028609	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs148500327	chr9:72028628-72028629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs35249143	chr9:72028643-72028644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370582631	chr9:72028646-72028647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566394580	chr9:72028652-72028653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs9410534	chr9:72028653-72028654	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs114304481	chr9:72028654-72028655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs13289130	chr9:72028671-72028672	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs76131241	chr9:72028672-72028673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs150100254	chr9:72028684-72028685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185895159	chr9:72028689-72028690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536094745	chr9:72028701-72028702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs55924254	chr9:72028712-72028713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs76666871	chr9:72028719-72028720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs74845544	chr9:72028726-72028727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546135015	chr9:72028729-72028730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs77884467	chr9:72028730-72028731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs79941210	chr9:72028732-72028733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs9410823	chr9:72028736-72028737	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs77787279	chr9:72028740-72028741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs80204230	chr9:72028741-72028742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs77500802	chr9:72028755-72028756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79673485	chr9:72028760-72028761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs28386177	chr9:72028761-72028762	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs80305139	chr9:72028766-72028767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs80193128	chr9:72028771-72028772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs80225774	chr9:72028776-72028777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188403789	chr9:72028781-72028782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs368157265	chr9:72028837-72028838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529047924	chr9:72028885-72028886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112701679	chr9:72028899-72028900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs36168803	chr9:72028923-72028924	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs146997377	chr9:72028946-72028947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs28505427	chr9:72028961-72028962	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs532805780	chr9:72028979-72028980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551329625	chr9:72029050-72029051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1752110	chr9:72029069-72029070	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs566458009	chr9:72029103-72029104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12995733	chr9:72029116-72029117	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs527566714	chr9:72029117-72029118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548804671	chr9:72029135-72029136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs36011603	chr9:72029151-72029152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537997257	chr9:72029153-72029154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569878082	chr9:72029164-72029165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17899364	CNVD
Mantle cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:259 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72026800-72028400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:72027000-72028400	Enhancers	Esophagus	oesophagus
3	chr9:72027000-72040000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr9:72027800-72028400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:72027800-72028400	Enhancers	Brain Angular Gyrus	brain
6	chr9:72027800-72028400	Enhancers	Brain Cingulate Gyrus	brain
7	chr9:72028000-72028400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr9:72028000-72028400	Enhancers	Lung	lung
9	chr9:72028000-72028400	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr9:72028200-72028400	Enhancers	Skeletal Muscle Male	skeletal muscle
11	chr9:72028200-72028400	Enhancers	Stomach Smooth Muscle	stomach
12	chr9:72028200-72028600	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr9:72033800-72034000	Enhancers	Stomach Mucosa	stomach
14	chr9:72036000-72036200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr9:72036000-72037600	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr9:72036200-72043000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr9:72036400-72037200	Enhancers	Skeletal Muscle Female	skeletal muscle
18	chr9:72036600-72082600	Weak transcription	Rectal Smooth Muscle	rectum
19	chr9:72036800-72037000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
20	chr9:72036800-72037200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr9:72036800-72037200	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr9:72036800-72037200	Enhancers	Stomach Mucosa	stomach
23	chr9:72036800-72037400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr9:72036800-72037600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr9:72036800-72045200	Weak transcription	Fetal Brain Female	brain
26	chr9:72037000-72037200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr9:72037000-72037200	Enhancers	Fetal Lung	lung
28	chr9:72037000-72037200	Enhancers	Fetal Muscle Leg	muscle
29	chr9:72037000-72037600	Enhancers	Brain Angular Gyrus	brain
30	chr9:72037000-72037600	Enhancers	Brain Cingulate Gyrus	brain
31	chr9:72037000-72037600	Enhancers	Brain Hippocampus Middle	brain
32	chr9:72037000-72037600	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr9:72037000-72037600	Enhancers	Brain Substantia Nigra	brain
34	chr9:72037000-72037600	Enhancers	Fetal Stomach	stomach
35	chr9:72037200-72037600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
36	chr9:72037200-72037800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr9:72037200-72039800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr9:72037200-72040200	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr9:72037200-72046600	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr9:72037200-72048600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr9:72037200-72055600	Weak transcription	Fetal Lung	lung
42	chr9:72037200-72056200	Weak transcription	Fetal Muscle Leg	muscle
43	chr9:72037400-72037600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr9:72037400-72037600	Enhancers	Fetal Kidney	kidney
45	chr9:72037400-72037600	Enhancers	Stomach Smooth Muscle	stomach
46	chr9:72037400-72045200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr9:72037600-72039000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr9:72037600-72039400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr9:72037600-72039600	Weak transcription	Brain Hippocampus Middle	brain
50	chr9:72037600-72039600	Weak transcription	Brain Inferior Temporal Lobe	brain

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