Variant report

Variant	nsv1017145
Chromosome Location	chr7:126995304-127015459
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:221)
CpG islands
(count:61)
Chromatin interactive
region (count:22)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:221 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:127006950-127007157	K562	blood:	n/a	n/a
2	ARID3A	chr7:127005297-127006020	K562	blood:	n/a	n/a
3	ARID3A	chr7:127010357-127010543	K562	blood:	n/a	n/a
4	ARID3A	chr7:127002567-127003142	K562	blood:	n/a	n/a
5	ATF1	chr7:127002801-127003036	K562	blood:	n/a	n/a
6	BACH1	chr7:126995773-126996154	K562	blood:	n/a	n/a
7	BHLHE40	chr7:127002853-127002880	K562	blood:	n/a	n/a
8	CCNT2	chr7:127002846-127003044	K562	blood:	n/a	n/a
9	CCNT2	chr7:127005271-127006422	K562	blood:	n/a	chr7:127005416-127005436
10	CEBPB	chr7:127005321-127005576	K562	blood:	n/a	n/a
11	CEBPD	chr7:127005068-127006124	K562	blood:	n/a	n/a
12	CEBPD	chr7:127005100-127006104	K562	blood:	n/a	n/a
13	CHD2	chr7:127009406-127009547	K562	blood:	n/a	n/a
14	CHD2	chr7:127013748-127013862	K562	blood:	n/a	n/a
15	CTCF	chr7:127014640-127014790	K562	blood:	n/a	n/a
16	CTCF	chr7:127014740-127014890	GM12873	blood:	n/a	n/a
17	CUX1	chr7:127002898-127003091	K562	blood:	n/a	n/a
18	CUX1	chr7:127005261-127006062	K562	blood:	n/a	n/a
19	E2F4	chr7:127000730-127000892	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F4	chr7:127013110-127013310	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr7:126999836-127000005	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F4	chr7:127014442-127014536	MCF10A-Er-Src	breast:	n/a	n/a
23	EP300	chr7:127005994-127006072	GM12878	blood:	n/a	n/a
24	EP300	chr7:127002735-127003141	K562	blood:	n/a	n/a
25	EP300	chr7:127005307-127006124	K562	blood:	n/a	n/a
26	EP300	chr7:127006794-127007122	SK-N-SH_RA	brain:	n/a	n/a
27	EP300	chr7:127006675-127007183	SK-N-SH_RA	brain:	n/a	n/a
28	EP300	chr7:127001837-127001931	K562	blood:	n/a	n/a
29	EP300	chr7:127005164-127006671	K562	blood:	n/a	chr7:127006573-127006582
30	ESR1	chr7:126998998-126999357	T-47D	breast:	n/a	n/a
31	ESR1	chr7:126999060-126999341	T-47D	breast:	n/a	n/a
32	ESR1	chr7:126999111-126999368	T-47D	breast:	n/a	n/a
33	FOS	chr7:126995830-126995996	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr7:126995791-126996114	MCF10A-Er-Src	breast:	n/a	n/a
35	FOXA1	chr7:126999125-126999363	T-47D	breast:	n/a	n/a
36	FOXA1	chr7:126999129-126999372	T-47D	breast:	n/a	n/a
37	GATA1	chr7:127002731-127007242	K562	blood:	n/a	chr7:127005425-127005434 chr7:127005416-127005433 chr7:127005422-127005438
38	GATA1	chr7:127004874-127006499	PBDE	blood:	n/a	chr7:127005425-127005434 chr7:127005416-127005433 chr7:127005422-127005438
39	GATA2	chr7:127005162-127006078	K562	blood:	n/a	chr7:127005425-127005434 chr7:127005416-127005433 chr7:127005422-127005438
40	GATA2	chr7:127002713-127003140	K562	blood:	n/a	n/a
41	GATA2	chr7:127005162-127005644	K562	blood:	n/a	chr7:127005425-127005434 chr7:127005416-127005433 chr7:127005422-127005438
42	GATA3	chr7:127014924-127014975	SH-SY5Y	brain:	n/a	n/a
43	GATA3	chr7:127005276-127005466	SH-SY5Y	brain:	n/a	chr7:127005425-127005434 chr7:127005416-127005433 chr7:127005422-127005438
44	GATA3	chr7:127000596-127000661	SH-SY5Y	brain:	n/a	n/a
45	GATA3	chr7:126999770-126999924	SH-SY5Y	brain:	n/a	n/a
46	GATA3	chr7:126999098-126999348	T-47D	breast:	n/a	n/a
47	GATA3	chr7:126999094-126999393	MCF-7	breast:	n/a	n/a
48	GATA3	chr7:127006551-127006666	SH-SY5Y	brain:	n/a	n/a
49	GATA3	chr7:127008384-127008417	SH-SY5Y	brain:	n/a	n/a
50	GATA3	chr7:127002142-127002294	SH-SY5Y	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:127011849-127011899	AG09309	skin:	n/a
2	chr7:127011849-127011899	RPTEC	kidney:	n/a
3	chr7:127011849-127011899	GM06990	blood:	n/a
4	chr7:127011849-127011899	H1-hESC	embryonic stem cell:	embryo
5	chr7:127011849-127011899	NB4	blood:	n/a
6	chr7:127011849-127011899	HAEpiC	amniotic membrane:	n/a
7	chr7:127011849-127011899	GM12892	blood:	n/a
8	chr7:127011849-127011899	Hepatocyte	liver:	n/a
9	chr7:127011849-127011899	SAEC	small airway:	n/a
10	chr7:127011849-127011899	Hela-S3	cervix:	n/a
11	chr7:127011849-127011899	ProgFib	skin:	n/a
12	chr7:127011849-127011899	GM12878	blood:	n/a
13	chr7:127011849-127011899	HMEC	breast:	n/a
14	chr7:127011849-127011899	A549	lung:	n/a
15	chr7:127011849-127011899	PrEC	prostate:	n/a
16	chr7:127011849-127011899	K562	blood:	n/a
17	chr7:127011849-127011899	BJ	skin:	n/a
18	chr7:127011849-127011899	HIPEpiC	eye:	n/a
19	chr7:127011849-127011899	BE2_C	brain:	n/a
20	chr7:127011849-127011899	NH-A	brain:	n/a
21	chr7:127011849-127011899	ECC-1	luminal epithelium:	n/a
22	chr7:127011849-127011899	SKMC	muscle:	n/a
23	chr7:127011849-127011899	HCT-116	colon:	n/a
24	chr7:127011849-127011899	HCM	heart:	n/a
25	chr7:127011849-127011899	NT2-D1	testis:	n/a
26	chr7:127011849-127011899	SK-N-SH	brain:	n/a
27	chr7:127011849-127011899	U87	brain:	n/a
28	chr7:127011849-127011899	AG04450	lung:	fetal
29	chr7:127011849-127011899	AoSMC	blood vessel:	n/a
30	chr7:127011849-127011899	HCF	heart:	n/a
31	chr7:127011849-127011899	ovcar-3	ovarian:	n/a
32	chr7:127011849-127011899	PANC-1	pancreas:	n/a
33	chr7:127011849-127011899	CMK	blood:	n/a
34	chr7:127011849-127011899	HCPEpiC	choroid plexus:	n/a
35	chr7:127011849-127011899	T-47D	breast:	n/a
36	chr7:127011849-127011899	AG04449	skin:	fetal
37	chr7:127011849-127011899	LNCaP	prostate:	n/a
38	chr7:127011849-127011899	HL-60	blood:	n/a
39	chr7:127011849-127011899	GM19239	blood:	n/a
40	chr7:127011849-127011899	HepG2	liver:	n/a
41	chr7:127011849-127011899	HNPCEpiC	eye:	n/a
42	chr7:127011849-127011899	HPAEpiC	pulmonary alveolar:	n/a
43	chr7:127011849-127011899	NHBE	bronchial:	n/a
44	chr7:127011849-127011899	GM12891	blood:	n/a
45	chr7:127011849-127011899	HRE	kidney:	n/a
46	chr7:127011849-127011899	IMR90	lung:	fetal
47	chr7:127011849-127011899	AG10803	skin:	n/a
48	chr7:127011849-127011899	HRCEpiC	kidney:	n/a
49	chr7:127011849-127011899	HUVEC	blood vessel:	n/a
50	chr7:127011849-127011899	MCF-7	breast:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:126999289..127001644-chr7:127001695..127003278,2	MCF-7	breast:
2	chr7:126994441..126996750-chr7:126997785..127000283,3	K562	blood:
3	chr7:126992206..126994276-chr7:126998893..127000633,3	K562	blood:
4	chr7:126893732..126895403-chr7:127004899..127007535,2	K562	blood:
5	chr7:126982960..126985576-chr7:127008832..127010898,2	K562	blood:
6	chr7:127008141..127011096-chr7:127031211..127032918,3	MCF-7	breast:
7	chr7:126985529..126987852-chr7:126995561..126998469,2	K562	blood:
8	chr7:127011088..127012818-chr7:127232951..127235470,2	K562	blood:
9	chr7:126999623..127001403-chr7:127005210..127006767,2	MCF-7	breast:
10	chr7:127002102..127004107-chr7:127029978..127032429,2	MCF-7	breast:
11	chr7:127002727..127005442-chr7:127031121..127033486,2	MCF-7	breast:
12	chr7:127013823..127015745-chr7:127047033..127049146,2	K562	blood:
13	chr7:126989599..126991125-chr7:126999110..127001691,2	K562	blood:
14	chr7:127014796..127019134-chr7:127031317..127035078,8	MCF-7	breast:
15	chr7:126993441..126998972-chr7:127031083..127033725,7	MCF-7	breast:
16	chr7:127007429..127009015-chr7:127025280..127028276,2	MCF-7	breast:
17	chr7:126999289..127001644-chr7:127001695..127003278,2	MCF-7	breast:
18	chr7:127005088..127006820-chr7:127013263..127015171,2	MCF-7	breast:
19	chr7:126999623..127001403-chr7:127005210..127006767,2	MCF-7	breast:
20	chr7:126994441..126996750-chr7:126997785..127000283,3	K562	blood:
21	chr7:127011403..127015656-chr7:127030018..127033626,5	MCF-7	breast:
22	chr7:127009044..127010892-chr7:127015747..127017535,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARF5-11	chr7:127012159-127012646	ncRnaDb_ncrna_FR178743_1
2	lnc-ZNF800-2	chr7:126999844-127004813	NONHSAT123138

No data

(count:9 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	ZNF800	hsa-miR-101-3p	chr7:127010881-127010901
2	ZNF800	hsa-miR-128-3p	chr7:127012929-127012949
3	ZNF800	hsa-miR-27a-3p	chr7:127012905-127012925
4	ZNF800	hsa-miR-128-3p	chr7:127010526-127010546
5	ZNF800	hsa-miR-27a-3p	chr7:127010531-127010524
6	ZNF800	hsa-miR-101-3p	chr7:127010527-127010547
7	ZNF800	hsa-miR-27a-3p	chr7:127010525-127010543
8	ZNF800	hsa-miR-335-5p	chr7:127010462-127010484
9	ZNF800	hsa-miR-101-3p	chr7:127011650-127011669

Variant related genes	Relation type
ZNF800	TF binding region
ZNF800	CpG island
ENSG00000106328	chromatin interactions
ENSG00000179562	chromatin interactions
ENSG00000224138	chromatin interactions
ENSG00000048405	chromatin interactions

Extended variants
information (count: 770 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:770 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10235028	chr7:126995304-126995305	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs570822169	chr7:126995311-126995312	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs17866442	chr7:126995321-126995322	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs534746161	chr7:126995358-126995359	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs150887964	chr7:126995373-126995374	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs566160372	chr7:126995376-126995377	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs10487478	chr7:126995414-126995415	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs554329263	chr7:126995427-126995428	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs575862296	chr7:126995428-126995429	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs561064104	chr7:126995463-126995464	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs117479436	chr7:126995494-126995495	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs17864970	chr7:126995582-126995583	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs540851310	chr7:126995616-126995617	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs532094183	chr7:126995633-126995634	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs367617176	chr7:126995645-126995646	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs139347915	chr7:126995698-126995699	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs17865875	chr7:126995765-126995766	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs532882500	chr7:126995773-126995774	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs190931337	chr7:126995798-126995799	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs149917405	chr7:126995815-126995816	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs201012347	chr7:126995945-126995946	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs143947413	chr7:126996025-126996026	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs182758794	chr7:126996031-126996032	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs117744062	chr7:126996107-126996108	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs17867831	chr7:126996112-126996113	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs17864930	chr7:126996118-126996119	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs553113416	chr7:126996153-126996154	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs568152532	chr7:126996178-126996179	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs535533773	chr7:126996229-126996230	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs188881439	chr7:126996285-126996286	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs569310339	chr7:126996310-126996311	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs575823360	chr7:126996321-126996322	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs199663640	chr7:126996323-126996324	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs200660058	chr7:126996324-126996325	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs533730547	chr7:126996325-126996326	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs372235180	chr7:126996326-126996327	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs202012438	chr7:126996334-126996335	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs58534362	chr7:126996335-126996336	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs200134865	chr7:126996336-126996337	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs17867358	chr7:126996348-126996349	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs191112451	chr7:126996352-126996353	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs17863283	chr7:126996356-126996357	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs140358962	chr7:126996388-126996389	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs558771892	chr7:126996389-126996390	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs577086741	chr7:126996464-126996465	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs540988739	chr7:126996616-126996617	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs559068708	chr7:126996621-126996622	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs71179572	chr7:126996631-126996632	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs529740744	chr7:126996654-126996655	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs183253018	chr7:126996682-126996683	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	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
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
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Autism	20808228	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:570 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:126984400-127000800	Weak transcription	HSMMtube	muscle
2	chr7:126987200-126995400	Weak transcription	Dnd41	blood
3	chr7:126987800-127020600	Weak transcription	Spleen	Spleen
4	chr7:126988200-127001000	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr7:126988400-126995400	Weak transcription	Primary B cells from cord blood	blood
6	chr7:126988400-126995400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr7:126988400-126995600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr7:126988400-126996000	Weak transcription	NHDF-Ad	bronchial
9	chr7:126988400-126996800	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr7:126988400-126997000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr7:126988400-126997000	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr7:126988400-126997000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr7:126988400-126997000	Weak transcription	Osteobl	bone
14	chr7:126988400-126998800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr7:126988400-126998800	Weak transcription	Placenta	Placenta
16	chr7:126988400-126999200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr7:126988400-126999200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr7:126988400-126999800	Weak transcription	Primary T cells from cord blood	blood
19	chr7:126988400-127000000	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr7:126988400-127000000	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr7:126988400-127000000	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr7:126988400-127000200	Weak transcription	Adipose Nuclei	Adipose
23	chr7:126988400-127000400	Weak transcription	Hela-S3	cervix
24	chr7:126988400-127000600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr7:126988400-127000600	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr7:126988400-127000600	Weak transcription	Fetal Intestine Large	intestine
27	chr7:126988400-127000800	Weak transcription	Primary B cells from peripheral blood	blood
28	chr7:126988400-127000800	Weak transcription	Brain Hippocampus Middle	brain
29	chr7:126988400-127000800	Weak transcription	Duodenum Mucosa	Duodenum
30	chr7:126988400-127000800	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr7:126988400-127001000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr7:126988400-127001000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr7:126988400-127001000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr7:126988400-127001000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr7:126988400-127001000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr7:126988400-127001000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr7:126988400-127001000	Weak transcription	Aorta	Aorta
38	chr7:126988400-127001000	Weak transcription	Brain Angular Gyrus	brain
39	chr7:126988400-127001000	Weak transcription	Esophagus	oesophagus
40	chr7:126988400-127001000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr7:126988400-127001000	Weak transcription	Fetal Stomach	stomach
42	chr7:126988400-127001000	Weak transcription	Left Ventricle	heart
43	chr7:126988400-127001000	Weak transcription	Lung	lung
44	chr7:126988400-127001000	Weak transcription	Right Ventricle	heart
45	chr7:126988400-127001000	Weak transcription	Thymus	Thymus
46	chr7:126988400-127001000	Weak transcription	NH-A	brain
47	chr7:126988400-127001000	Weak transcription	NHLF	lung
48	chr7:126988400-127001200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr7:126988400-127002200	Weak transcription	Fetal Heart	heart
50	chr7:126988400-127004400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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