Variant report

Variant	esv1799806
Chromosome Location	chr7:120997195-121008204
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	chr7:121006892-121007261	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:121006929-121007286	K562	blood:	n/a	n/a
3	CEBPB	chr7:121007853-121008109	HepG2	liver:	n/a	chr7:121007970-121007981
4	CEBPB	chr7:121007822-121008126	H1-hESC	embryonic stem cell:	n/a	chr7:121007970-121007981
5	CEBPB	chr7:121007849-121008056	IMR90	lung:	n/a	chr7:121007970-121007981
6	CEBPB	chr7:121006966-121007210	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr7:121007839-121008135	K562	blood:	n/a	chr7:121007970-121007981
8	CTCF	chr7:121007020-121007170	HPF	lung:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
9	CTCF	chr7:121007020-121007170	HBMEC	blood vessel:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
10	CTCF	chr7:121007020-121007170	HEEpiC	esophagus:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
11	CTCF	chr7:121007000-121007150	NHDF-neo	bronchial:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
12	CTCF	chr7:121006935-121007204	HUVEC	blood vessel:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
13	CTCF	chr7:121006940-121007254	A549	lung:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
14	CTCF	chr7:121006866-121007245	A549	lung:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
15	CTCF	chr7:121006980-121007130	HMF	breast:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
16	CTCF	chr7:121006890-121007141	A549	lung:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
17	CTCF	chr7:121007020-121007170	GM12864	blood:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
18	CTCF	chr7:121006911-121007245	Spleen_OC	spleen:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
19	CTCF	chr7:121006940-121007090	HFF-Myc	foreskin:	n/a	chr7:121007077-121007090
20	CTCF	chr7:121007060-121007210	WI-38	lung:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
21	CTCF	chr7:121006940-121007090	HA-sp	spinal cord:	n/a	chr7:121007077-121007090
22	CTCF	chr7:121006980-121007130	GM06990	blood:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
23	CTCF	chr7:121006980-121007130	GM12868	blood:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
24	CTCF	chr7:121007000-121007150	HCT-116	colon:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
25	CTCF	chr7:121007020-121007170	HCPEpiC	choroid plexus:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
26	CTCF	chr7:121007000-121007150	AG10803	skin:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
27	CTCF	chr7:121006978-121007178	GM10266	blood:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
28	CTCF	chr7:121006787-121007313	HCT-116	colon:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
29	CTCF	chr7:121006918-121007216	Medullo	brain:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
30	CTCF	chr7:121006960-121007110	HMEC	breast:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
31	CTCF	chr7:121006940-121007090	GM12864	blood:	n/a	chr7:121007077-121007090
32	CTCF	chr7:121007020-121007170	HAc	cerebellar:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
33	CTCF	chr7:121007020-121007170	GM12870	blood:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
34	CTCF	chr7:121006980-121007130	AG09319	gingival:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
35	CTCF	chr7:121006980-121007130	GM12801	blood:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
36	CTCF	chr7:121007000-121007150	HepG2	liver:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
37	CTCF	chr7:121007020-121007170	HA-sp	spinal cord:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
38	CTCF	chr7:121007020-121007170	HRE	kidney:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
39	CTCF	chr7:121006829-121007340	MCF-7	breast:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
40	CTCF	chr7:121007000-121007150	Hela-S3	cervix:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
41	CTCF	chr7:121006940-121007090	NHLF	lung:	n/a	chr7:121007077-121007090
42	CTCF	chr7:121006900-121007050	HAc	cerebellar:	n/a	n/a
43	CTCF	chr7:121006960-121007110	HVMF	connective:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
44	CTCF	chr7:121007000-121007150	GM12869	blood:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
45	CTCF	chr7:121007192-121007194	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr7:121007000-121007150	HPAF	blood vessel:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
47	CTCF	chr7:121006804-121007444	HCT-116	colon:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
48	CTCF	chr7:121006864-121007196	SK-N-SH_RA	brain:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
49	CTCF	chr7:121006980-121007130	MCF-7	breast:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090
50	CTCF	chr7:121007020-121007170	GM12878	blood:	n/a	chr7:121007076-121007097 chr7:121007074-121007092 chr7:121007077-121007090

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:121006948-121006998	MCF10A-Er-Src	breast:	n/a
2	chr7:121006948-121006998	HIPEpiC	eye:	n/a
3	chr7:121006948-121006998	NH-A	brain:	n/a
4	chr7:121006948-121006998	NB4	blood:	n/a
5	chr7:121006948-121006998	HMEC	breast:	n/a
6	chr7:121006948-121006998	HEEpiC	esophagus:	n/a
7	chr7:121006948-121006998	NHBE	bronchial:	n/a
8	chr7:121006948-121006998	ovcar-3	ovarian:	n/a
9	chr7:121006948-121006998	AG04450	lung:	fetal
10	chr7:121006948-121006998	Hela-S3	cervix:	n/a
11	chr7:121006948-121006998	RPTEC	kidney:	n/a
12	chr7:121006948-121006998	GM19239	blood:	n/a
13	chr7:121006948-121006998	PFSK-1	brain:	n/a
14	chr7:121006948-121006998	K562	blood:	n/a
15	chr7:121006948-121006998	SK-N-SH	brain:	n/a
16	chr7:121006948-121006998	PANC-1	pancreas:	n/a
17	chr7:121006948-121006998	HRE	kidney:	n/a
18	chr7:121006948-121006998	Hepatocyte	liver:	n/a
19	chr7:121006948-121006998	HL-60	blood:	n/a
20	chr7:121006948-121006998	SK-N-MC	brain:	n/a
21	chr7:121006948-121006998	AG04449	skin:	fetal
22	chr7:121006948-121006998	HCPEpiC	choroid plexus:	n/a
23	chr7:121006948-121006998	Jurkat	blood:	n/a
24	chr7:121006948-121006998	BE2_C	brain:	n/a
25	chr7:121006948-121006998	Caco-2	colon:	n/a
26	chr7:121006948-121006998	GM12892	blood:	n/a
27	chr7:121006948-121006998	IMR90	lung:	fetal
28	chr7:121006948-121006998	LNCaP	prostate:	n/a
29	chr7:121006948-121006998	HEK293	kidney:	embryo
30	chr7:121006948-121006998	GM06990	blood:	n/a
31	chr7:121006948-121006998	CMK	blood:	n/a
32	chr7:121006948-121006998	SK-N-SH_RA	brain:	n/a
33	chr7:121006948-121006998	HUVEC	blood vessel:	n/a
34	chr7:121006948-121006998	T-47D	breast:	n/a
35	chr7:121006948-121006998	AG09319	gingival:	n/a
36	chr7:121006948-121006998	AG10803	skin:	n/a
37	chr7:121006948-121006998	SAEC	small airway:	n/a
38	chr7:121006948-121006998	GM12878	blood:	n/a
39	chr7:121006948-121006998	U87	brain:	n/a
40	chr7:121006948-121006998	AoSMC	blood vessel:	n/a
41	chr7:121006948-121006998	HepG2	liver:	n/a
42	chr7:121006948-121006998	HRCEpiC	kidney:	n/a
43	chr7:121006948-121006998	HCT-116	colon:	n/a
44	chr7:121006948-121006998	HPAEpiC	pulmonary alveolar:	n/a
45	chr7:121006948-121006998	SKMC	muscle:	n/a
46	chr7:121006948-121006998	NT2-D1	testis:	n/a
47	chr7:121006948-121006998	PrEC	prostate:	n/a
48	chr7:121006948-121006998	BJ	skin:	n/a
49	chr7:121006948-121006998	HCM	heart:	n/a
50	chr7:121006948-121006998	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:121005362..121009236-chr7:121034882..121036635,4	MCF-7	breast:
2	chr17:57920914..57923134-chr7:121006073..121007624,2	MCF-7	breast:
3	chr7:121006747..121007563-chr7:121149688..121150676,2	K562	blood:
4	chr7:121006680..121008574-chr7:121018807..121020891,2	K562	blood:
5	chr7:121007069..121007588-chr7:121634575..121635222,2	K562	blood:
6	chr7:120994379..120997968-chr7:121032765..121037049,4	K562	blood:
7	chr7:120993925..120996278-chr7:120998295..120999894,2	MCF-7	breast:
8	chr7:121006586..121008267-chr7:121187006..121188236,8	MCF-7	breast:
9	chr7:121004060..121005597-chr7:121034745..121036816,2	K562	blood:
10	chr7:121006632..121007533-chr7:121634434..121635294,2	MCF-7	breast:
11	chr7:121007820..121010026-chr7:121078337..121080058,2	K562	blood:
12	chr7:120945110..120947214-chr7:120997480..120999787,2	K562	blood:
13	chr7:121007156..121009116-chr7:121011586..121013929,2	K562	blood:
14	chr7:120996529..120999253-chr7:121021354..121023479,2	K562	blood:
15	chr7:120998130..121000230-chr7:121033883..121036363,2	MCF-7	breast:
16	chr7:120984176..120986592-chr7:121005474..121007076,2	MCF-7	breast:
17	chr7:120991538..120993968-chr7:120997177..121000035,2	MCF-7	breast:
18	chr7:121007095..121012773-chr7:121032215..121038175,10	MCF-7	breast:
19	chr7:121006580..121008366-chr7:121155081..121156610,2	K562	blood:
20	chr7:120999680..121002085-chr7:121003429..121005144,2	K562	blood:
21	chr7:121006292..121008390-chr7:121186488..121188741,23	K562	blood:
22	chr7:121006823..121007565-chr7:121187243..121187877,3	MCF-7	breast:
23	chr7:121007055..121007746-chr7:121036256..121036915,3	K562	blood:
24	chr7:120995819..120998464-chr7:121018904..121020746,2	K562	blood:

Variant related genes	Relation type
FAM3C	TF binding region
FAM3C	CpG island
ENSG00000196937	chromatin interactions

Extended variants
information (count: 382 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:382 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545317318	chr7:120997203-120997204	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs115503140	chr7:120997233-120997234	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs542647692	chr7:120997243-120997244	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs143762132	chr7:120997262-120997263	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs572055744	chr7:120997275-120997276	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs540783165	chr7:120997288-120997289	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs367961379	chr7:120997295-120997296	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs146880813	chr7:120997309-120997310	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs564899909	chr7:120997325-120997326	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs532856281	chr7:120997337-120997338	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs148994390	chr7:120997352-120997353	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs2707505	chr7:120997369-120997370	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs528863091	chr7:120997370-120997371	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs549037634	chr7:120997399-120997400	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs566370786	chr7:120997400-120997401	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs567386365	chr7:120997412-120997413	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs550709076	chr7:120997445-120997446	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs567219535	chr7:120997468-120997469	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs571825884	chr7:120997507-120997508	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs2536172	chr7:120997560-120997561	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs543007440	chr7:120997582-120997583	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs374988269	chr7:120997591-120997592	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs186994849	chr7:120997606-120997607	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs556268792	chr7:120997620-120997621	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs191063735	chr7:120997621-120997622	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs552953405	chr7:120997648-120997649	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs571972012	chr7:120997657-120997658	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs540946350	chr7:120997661-120997662	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs564100219	chr7:120997712-120997713	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs182728289	chr7:120997731-120997732	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs543284636	chr7:120997770-120997771	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs564497493	chr7:120997783-120997784	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs529043327	chr7:120997835-120997836	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs558810549	chr7:120997864-120997865	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs568927069	chr7:120997901-120997902	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs542595908	chr7:120997942-120997943	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs559399536	chr7:120997983-120997984	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs528761102	chr7:120997989-120997990	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs537820734	chr7:120998003-120998004	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs552123767	chr7:120998012-120998013	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs368787487	chr7:120998053-120998054	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs35682832	chr7:120998085-120998086	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs397712986	chr7:120998086-120998087	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs142536540	chr7:120998108-120998109	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs186779818	chr7:120998112-120998113	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs574798031	chr7:120998126-120998127	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs191869734	chr7:120998131-120998132	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs550940672	chr7:120998148-120998149	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs182609810	chr7:120998164-120998165	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs187557340	chr7:120998165-120998166	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	21115979	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:388 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:120970600-121016800	Weak transcription	Gastric	stomach
2	chr7:120970600-121025400	Weak transcription	Spleen	Spleen
3	chr7:120970800-121000400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr7:120973800-120998800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr7:120977800-120999800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr7:120978800-121017400	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr7:120979800-121019400	Weak transcription	Thymus	Thymus
8	chr7:120979800-121034800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr7:120980800-121019600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr7:120981000-121015200	Weak transcription	Pancreas	Pancrea
11	chr7:120983000-121009600	Weak transcription	Hela-S3	cervix
12	chr7:120983800-121000200	Weak transcription	Fetal Kidney	kidney
13	chr7:120984000-121017600	Weak transcription	Brain Cingulate Gyrus	brain
14	chr7:120984200-121001200	Weak transcription	NHLF	lung
15	chr7:120984200-121009800	Weak transcription	Fetal Brain Male	brain
16	chr7:120984200-121035000	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr7:120984800-121009600	Weak transcription	A549	lung
18	chr7:120985000-121001200	Weak transcription	Brain Hippocampus Middle	brain
19	chr7:120985000-121009600	Weak transcription	Small Intestine	intestine
20	chr7:120985200-121000000	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr7:120985200-121013000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr7:120986200-121029600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr7:120986400-121026000	Weak transcription	Colonic Mucosa	Colon
24	chr7:120986400-121026000	Weak transcription	Psoas Muscle	Psoas
25	chr7:120987600-121003800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr7:120989200-120999000	Weak transcription	HepG2	liver
27	chr7:120989200-121015400	Weak transcription	Brain Anterior Caudate	brain
28	chr7:120989600-121016800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr7:120990400-120998800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr7:120990400-121002400	Strong transcription	NH-A	brain
31	chr7:120990400-121005000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr7:120990400-121005200	Strong transcription	Dnd41	blood
33	chr7:120990400-121006000	Strong transcription	Primary B cells from peripheral blood	blood
34	chr7:120990400-121006200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr7:120990400-121007000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr7:120990400-121008600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr7:120990600-120998000	Strong transcription	HUES64 Cell Line	embryonic stem cell
38	chr7:120990600-120998000	Strong transcription	Fetal Intestine Large	intestine
39	chr7:120990600-120998200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
40	chr7:120990600-120998800	Strong transcription	Osteobl	bone
41	chr7:120990600-121000000	Strong transcription	NHDF-Ad	bronchial
42	chr7:120990600-121004200	Strong transcription	Primary T helper cells fromperipheralblood	blood
43	chr7:120990600-121004800	Strong transcription	Muscle Satellite Cultured Cells	--
44	chr7:120990600-121005000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr7:120990600-121006600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr7:120990600-121008800	Strong transcription	Duodenum Mucosa	Duodenum
47	chr7:120990600-121009000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr7:120990600-121009000	Strong transcription	HSMM	muscle
49	chr7:120991000-121012600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
50	chr7:120991200-121005200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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