Variant report

Variant	esv2759559
Chromosome Location	chr7:121059871-121089955
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:572)
CpG islands
(count:62)
Chromatin interactive
region (count:44)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:572 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:121077898-121078751	K562	blood:	n/a	n/a
2	ARID3A	chr7:121068861-121068867	K562	blood:	n/a	n/a
3	ATF1	chr7:121078557-121078820	K562	blood:	n/a	n/a
4	BATF	chr7:121072659-121072930	GM12878	blood:	n/a	n/a
5	BATF	chr7:121072589-121072929	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:121078559-121078630	K562	blood:	n/a	n/a
7	BHLHE40	chr7:121080992-121081288	K562	blood:	n/a	n/a
8	BHLHE40	chr7:121072735-121072838	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:121088228-121088300	K562	blood:	n/a	n/a
10	BHLHE40	chr7:121072202-121072228	K562	blood:	n/a	n/a
11	CBX3	chr7:121076652-121077218	K562	blood:	n/a	n/a
12	CBX3	chr7:121078346-121078975	K562	blood:	n/a	n/a
13	CBX3	chr7:121089318-121089813	HCT-116	colon:	n/a	n/a
14	CBX3	chr7:121078412-121078872	K562	blood:	n/a	n/a
15	CCNT2	chr7:121078573-121078770	K562	blood:	n/a	n/a
16	CEBPB	chr7:121066769-121066773	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr7:121068957-121069302	IMR90	lung:	n/a	chr7:121069129-121069140
18	CEBPB	chr7:121085267-121085500	K562	blood:	n/a	n/a
19	CEBPB	chr7:121068965-121069304	Hela-S3	cervix:	n/a	chr7:121069129-121069140
20	CEBPB	chr7:121088560-121088864	K562	blood:	n/a	n/a
21	CEBPB	chr7:121069875-121070201	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr7:121069037-121069263	HepG2	liver:	n/a	chr7:121069129-121069140
23	CEBPB	chr7:121070662-121070998	K562	blood:	n/a	n/a
24	CEBPB	chr7:121068873-121069337	ECC-1	luminal epithelium:	n/a	chr7:121069129-121069140
25	CEBPB	chr7:121088635-121088813	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr7:121086624-121086997	MCF-7	breast:	n/a	n/a
27	CEBPB	chr7:121068891-121069388	ECC-1	luminal epithelium:	n/a	chr7:121069129-121069140
28	CEBPB	chr7:121059616-121059919	HepG2	liver:	n/a	n/a
29	CEBPB	chr7:121061004-121061511	MCF-7	breast:	n/a	n/a
30	CEBPB	chr7:121061168-121061306	K562	blood:	n/a	n/a
31	CEBPB	chr7:121069916-121070146	HepG2	liver:	n/a	n/a
32	CEBPB	chr7:121086627-121086995	MCF-7	breast:	n/a	n/a
33	CEBPB	chr7:121069033-121069281	K562	blood:	n/a	chr7:121069129-121069140
34	CEBPB	chr7:121061041-121061497	MCF-7	breast:	n/a	n/a
35	CEBPB	chr7:121078690-121078713	K562	blood:	n/a	n/a
36	CEBPB	chr7:121088651-121088811	A549	lung:	n/a	n/a
37	CEBPB	chr7:121069010-121069280	H1-hESC	embryonic stem cell:	n/a	chr7:121069129-121069140
38	CHD1	chr7:121072869-121072991	GM12878	blood:	n/a	n/a
39	CHD2	chr7:121078248-121078820	GM12878	blood:	n/a	n/a
40	CHD2	chr7:121078577-121078891	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr7:121078631-121078714	HepG2	liver:	n/a	n/a
42	CHD2	chr7:121078396-121078820	K562	blood:	n/a	n/a
43	CTCF	chr7:121078560-121078710	GM12864	blood:	n/a	n/a
44	CTCF	chr7:121078480-121078630	GM12864	blood:	n/a	n/a
45	CTCF	chr7:121089381-121089741	K562	blood:	n/a	n/a
46	CTCF	chr7:121078500-121078650	GM12868	blood:	n/a	n/a
47	CTCF	chr7:121089340-121089490	HVMF	connective:	n/a	n/a
48	CTCF	chr7:121078540-121078690	GM12873	blood:	n/a	n/a
49	CTCF	chr7:121089440-121089590	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr7:121078480-121078630	WI-38	lung:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:121078303-121078353	GM12891	blood:	n/a
2	chr7:121078303-121078353	GM12891	blood:	n/a
3	chr7:121078303-121078353	HUVEC	blood vessel:	n/a
4	chr7:121078303-121078353	GM06990	blood:	n/a
5	chr7:121078303-121078353	HMEC	breast:	n/a
6	chr7:121078303-121078353	HPAEpiC	pulmonary alveolar:	n/a
7	chr7:121078303-121078353	HIPEpiC	eye:	n/a
8	chr7:121078303-121078353	PANC-1	pancreas:	n/a
9	chr7:121078303-121078353	GM19239	blood:	n/a
10	chr7:121078303-121078353	HAEpiC	amniotic membrane:	n/a
11	chr7:121078303-121078353	SAEC	small airway:	n/a
12	chr7:121078303-121078353	AG10803	skin:	n/a
13	chr7:121078303-121078353	HCF	heart:	n/a
14	chr7:121078303-121078353	AG09309	skin:	n/a
15	chr7:121078303-121078353	Caco-2	colon:	n/a
16	chr7:121078303-121078353	RPTEC	kidney:	n/a
17	chr7:121078303-121078353	H1-hESC	embryonic stem cell:	embryo
18	chr7:121078303-121078353	SK-N-SH_RA	brain:	n/a
19	chr7:121078303-121078353	ovcar-3	ovarian:	n/a
20	chr7:121078303-121078353	AG04449	skin:	fetal
21	chr7:121078303-121078353	Jurkat	blood:	n/a
22	chr7:121078303-121078353	MCF-7	breast:	n/a
23	chr7:121078303-121078353	NHBE	bronchial:	n/a
24	chr7:121078303-121078353	HEK293	kidney:	embryo
25	chr7:121078303-121078353	HEEpiC	esophagus:	n/a
26	chr7:121078303-121078353	SKMC	muscle:	n/a
27	chr7:121078303-121078353	NH-A	brain:	n/a
28	chr7:121078303-121078353	ProgFib	skin:	n/a
29	chr7:121078303-121078353	HCT-116	colon:	n/a
30	chr7:121078303-121078353	ECC-1	luminal epithelium:	n/a
31	chr7:121078303-121078353	GM12892	blood:	n/a
32	chr7:121078303-121078353	U87	brain:	n/a
33	chr7:121078303-121078353	NHDF-neo	bronchial:	n/a
34	chr7:121078303-121078353	HRE	kidney:	n/a
35	chr7:121078303-121078353	NB4	blood:	n/a
36	chr7:121078303-121078353	SK-N-MC	brain:	n/a
37	chr7:121078303-121078353	Hepatocyte	liver:	n/a
38	chr7:121078303-121078353	AoSMC	blood vessel:	n/a
39	chr7:121078303-121078353	AG04450	lung:	fetal
40	chr7:121078303-121078353	BE2_C	brain:	n/a
41	chr7:121078303-121078353	SK-N-SH	brain:	n/a
42	chr7:121078303-121078353	HNPCEpiC	eye:	n/a
43	chr7:121078303-121078353	CMK	blood:	n/a
44	chr7:121078303-121078353	IMR90	lung:	fetal
45	chr7:121078303-121078353	K562	blood:	n/a
46	chr7:121078303-121078353	T-47D	breast:	n/a
47	chr7:121078303-121078353	GM12878	blood:	n/a
48	chr7:121078303-121078353	A549	lung:	n/a
49	chr7:121078303-121078353	AG09319	gingival:	n/a
50	chr7:121078303-121078353	MCF10A-Er-Src	breast:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:121031207..121033515-chr7:121081375..121082898,2	K562	blood:
2	chr7:121035082..121037539-chr7:121077999..121080365,3	MCF-7	breast:
3	chr7:121056504..121058923-chr7:121065551..121067066,2	K562	blood:
4	chr7:121086464..121088878-chr7:121090558..121092067,2	K562	blood:
5	chr7:121069870..121071528-chr7:121071586..121073268,2	K562	blood:
6	chr7:121073008..121075987-chr7:121081368..121083333,2	K562	blood:
7	chr7:121071062..121073741-chr7:121077858..121079960,2	MCF-7	breast:
8	chr7:121033106..121035000-chr7:121064896..121066806,2	K562	blood:
9	chr7:121034886..121037643-chr7:121057416..121062764,7	MCF-7	breast:
10	chr7:121082501..121084474-chr7:121087406..121089640,2	MCF-7	breast:
11	chr7:121089158..121090017-chr7:121187411..121188046,2	MCF-7	breast:
12	chr7:121063601..121065601-chr7:121068374..121070365,2	MCF-7	breast:
13	chr7:121071062..121073741-chr7:121077858..121079960,2	MCF-7	breast:
14	chr7:121034711..121037260-chr7:121068206..121070323,3	MCF-7	breast:
15	chr7:121084438..121087093-chr7:121100657..121102565,2	K562	blood:
16	chr7:121017884..121020146-chr7:121086694..121088827,2	K562	blood:
17	chr7:121082938..121085924-chr7:121112606..121114729,2	K562	blood:
18	chr7:121072404..121074478-chr7:121078211..121080066,2	K562	blood:
19	chr7:121036172..121037993-chr7:121066052..121068787,2	MCF-7	breast:
20	chr7:121054965..121059361-chr7:121059382..121061611,4	K562	blood:
21	chr7:121072404..121074478-chr7:121078211..121080066,2	K562	blood:
22	chr7:121084590..121086129-chr7:121087840..121089417,2	K562	blood:
23	chr7:121028108..121030349-chr7:121074356..121077552,3	K562	blood:
24	chr5:43040736..43042911-chr7:121084118..121086879,2	MCF-7	breast:
25	chr7:121059489..121061007-chr7:121064201..121066957,2	K562	blood:
26	chr7:121007820..121010026-chr7:121078337..121080058,2	K562	blood:
27	chr7:121023385..121024908-chr7:121069353..121072128,2	K562	blood:
28	chr7:120994398..120996999-chr7:121076063..121078486,2	K562	blood:
29	chr7:121035131..121037238-chr7:121077312..121078831,2	K562	blood:
30	chr7:121084590..121086129-chr7:121087840..121089417,2	K562	blood:
31	chr7:121063601..121065601-chr7:121068374..121070365,2	MCF-7	breast:
32	chr7:121034708..121036424-chr7:121085034..121087096,2	K562	blood:
33	chr7:121034569..121037516-chr7:121059482..121062540,3	MCF-7	breast:
34	chr7:121034606..121036453-chr7:121075396..121077581,2	MCF-7	breast:
35	chr7:121060143..121062548-chr7:121064145..121066050,2	MCF-7	breast:
36	chr7:121059489..121061007-chr7:121064201..121066957,2	K562	blood:
37	chr7:121084429..121087093-chr7:121100657..121103964,3	K562	blood:
38	chr7:121082501..121084474-chr7:121087406..121089640,2	MCF-7	breast:
39	chr7:121035002..121037392-chr7:121079786..121082049,2	K562	blood:
40	chr7:121069870..121071528-chr7:121071586..121073268,2	K562	blood:
41	chr7:121054365..121057910-chr7:121059475..121061785,3	K562	blood:
42	chr7:121035103..121038034-chr7:121076504..121078587,5	K562	blood:
43	chr7:121073008..121075987-chr7:121081368..121083333,2	K562	blood:
44	chr7:121060143..121062548-chr7:121064145..121066050,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WNT16-2	chr7:121059806-121059899	NONHSAT123007

No data

Variant related genes	Relation type
ENSG00000234985	TF binding region
ENSG00000234985	CpG island
ENSG00000227371	chromatin interactions
ENSG00000215068	chromatin interactions
ENSG00000196937	chromatin interactions

Extended variants
information (count: 1289 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1289 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2707500	chr7:121059871-121059872	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs11974013	chr7:121059891-121059892	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs188722700	chr7:121059933-121059934	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs569778530	chr7:121059956-121059957	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs143505470	chr7:121059996-121059997	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs535562992	chr7:121060021-121060022	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs555294728	chr7:121060022-121060023	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs572449386	chr7:121060065-121060066	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs540145570	chr7:121060066-121060067	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs1534523	chr7:121060067-121060068	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs2141360	chr7:121060173-121060174	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs78994910	chr7:121060185-121060186	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs181103601	chr7:121060194-121060195	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs562683407	chr7:121060206-121060207	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs531390325	chr7:121060306-121060307	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs532870440	chr7:121060314-121060315	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs541995090	chr7:121060325-121060326	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs185412425	chr7:121060367-121060368	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs146745619	chr7:121060378-121060379	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs374850549	chr7:121060380-121060381	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs546165177	chr7:121060392-121060393	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs111271902	chr7:121060405-121060406	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs547749452	chr7:121060420-121060421	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs571094212	chr7:121060427-121060428	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs371134346	chr7:121060428-121060429	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs141226679	chr7:121060433-121060434	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs531707321	chr7:121060434-121060435	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs144936084	chr7:121060457-121060458	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs148337404	chr7:121060477-121060478	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs535549123	chr7:121060481-121060482	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs555481473	chr7:121060512-121060513	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs565919292	chr7:121060531-121060532	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs534989084	chr7:121060532-121060533	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs189841325	chr7:121060554-121060555	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs182473223	chr7:121060555-121060556	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs398095336	chr7:121060574-121060575	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs200124185	chr7:121060579-121060580	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs200908498	chr7:121060581-121060582	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs112146583	chr7:121060583-121060584	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs559540556	chr7:121060584-121060585	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs55902449	chr7:121060586-121060587	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs568523663	chr7:121060595-121060596	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs145599161	chr7:121060614-121060615	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs11281231	chr7:121060621-121060622	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs34145733	chr7:121060622-121060623	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs59798948	chr7:121060623-121060624	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs368360820	chr7:121060624-121060625	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs372449732	chr7:121060625-121060626	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs376742021	chr7:121060626-121060627	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs200449502	chr7:121060628-121060629	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

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

Chromatin state (count:523 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:121056800-121065800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr7:121058000-121062200	Enhancers	Fetal Intestine Small	intestine
3	chr7:121058800-121062000	Enhancers	Fetal Intestine Large	intestine
4	chr7:121059400-121060200	Bivalent Enhancer	Stomach Mucosa	stomach
5	chr7:121059400-121060400	Enhancers	Pancreas	Pancrea
6	chr7:121059400-121061800	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr7:121059400-121062200	Enhancers	Placenta	Placenta
8	chr7:121059600-121060200	Enhancers	Gastric	stomach
9	chr7:121059800-121060000	Enhancers	Esophagus	oesophagus
10	chr7:121059800-121062000	Enhancers	Duodenum Mucosa	Duodenum
11	chr7:121060200-121061600	Weak transcription	Gastric	stomach
12	chr7:121060200-121062000	Enhancers	Stomach Mucosa	stomach
13	chr7:121060400-121061400	Weak transcription	Pancreas	Pancrea
14	chr7:121060800-121061600	Enhancers	HMEC	breast
15	chr7:121061000-121061600	Enhancers	NHEK	skin
16	chr7:121061000-121061800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr7:121061200-121061600	Enhancers	K562	blood
18	chr7:121061400-121061800	Enhancers	Small Intestine	intestine
19	chr7:121061400-121062000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr7:121061400-121062000	Enhancers	Placenta Amnion	Placenta Amnion
21	chr7:121061400-121062200	Enhancers	Pancreas	Pancrea
22	chr7:121061600-121062000	Enhancers	Esophagus	oesophagus
23	chr7:121061600-121062000	Enhancers	Gastric	stomach
24	chr7:121065800-121066800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr7:121066600-121067000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr7:121066800-121067600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr7:121067000-121068800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr7:121067600-121070000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr7:121067800-121068400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr7:121068800-121069000	Enhancers	Placenta	Placenta
31	chr7:121068800-121069200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr7:121068800-121069200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr7:121068800-121069400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr7:121068800-121069400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr7:121068800-121069400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr7:121068800-121069600	Enhancers	Muscle Satellite Cultured Cells	--
37	chr7:121068800-121069600	Enhancers	Osteobl	bone
38	chr7:121068800-121069800	Enhancers	Fetal Kidney	kidney
39	chr7:121069000-121069200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr7:121069000-121069400	Enhancers	Placenta Amnion	Placenta Amnion
41	chr7:121069000-121069600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr7:121069000-121073400	Weak transcription	Placenta	Placenta
43	chr7:121069200-121069600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr7:121069200-121077600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr7:121069400-121074400	Weak transcription	Placenta Amnion	Placenta Amnion
46	chr7:121069800-121078000	Weak transcription	Fetal Kidney	kidney
47	chr7:121070800-121072400	Enhancers	Fetal Intestine Small	intestine
48	chr7:121071200-121072400	Enhancers	Fetal Intestine Large	intestine
49	chr7:121072000-121073000	Enhancers	GM12878-XiMat	blood
50	chr7:121072200-121077600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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