Variant report

Variant	nsv888834
Chromosome Location	chr7:102102343-102111796
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:992)
CpG islands
(count:1037)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:992 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102107670-102107707	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:102105026-102105477	HepG2	liver:	n/a	n/a
3	ATF2	chr7:102105214-102105642	GM12878	blood:	n/a	n/a
4	ATF3	chr7:102105121-102105483	H1-hESC	embryonic stem cell:	n/a	chr7:102105134-102105143
5	ATF3	chr7:102105156-102105479	HepG2	liver:	n/a	n/a
6	ATF3	chr7:102105079-102105666	K562	blood:	n/a	chr7:102105134-102105143
7	ATF3	chr7:102105052-102105541	A549	lung:	n/a	chr7:102105134-102105143
8	BACH1	chr7:102105195-102105583	K562	blood:	n/a	n/a
9	BACH1	chr7:102105152-102105627	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr7:102106969-102107235	GM12878	blood:	n/a	chr7:102107141-102107152
11	BCL3	chr7:102105600-102105954	A549	lung:	n/a	n/a
12	BCL3	chr7:102104786-102105505	A549	lung:	n/a	n/a
13	BCLAF1	chr7:102105007-102105737	GM12878	blood:	n/a	n/a
14	BCLAF1	chr7:102105109-102105696	K562	blood:	n/a	n/a
15	BHLHE40	chr7:102105028-102105670	K562	blood:	n/a	chr7:102105343-102105359 chr7:102105409-102105425
16	BHLHE40	chr7:102105053-102105547	GM12878	blood:	n/a	chr7:102105343-102105359 chr7:102105409-102105425
17	BHLHE40	chr7:102104315-102104322	K562	blood:	n/a	n/a
18	BRCA1	chr7:102105238-102105495	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr7:102107666-102107866	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr7:102107676-102107680	HepG2	liver:	n/a	n/a
21	BRCA1	chr7:102105131-102105589	HepG2	liver:	n/a	n/a
22	BRCA1	chr7:102105043-102105492	GM12878	blood:	n/a	n/a
23	CBX3	chr7:102104440-102105788	K562	blood:	n/a	n/a
24	CCNT2	chr7:102105109-102105718	K562	blood:	n/a	n/a
25	CCNT2	chr7:102109140-102109266	K562	blood:	n/a	n/a
26	CEBPB	chr7:102105268-102105644	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr7:102105250-102105458	GM12878	blood:	n/a	n/a
28	CEBPD	chr7:102105226-102105633	HepG2	liver:	n/a	n/a
29	CHD1	chr7:102105968-102105976	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD1	chr7:102105332-102105854	GM12878	blood:	n/a	n/a
31	CHD2	chr7:102105035-102105755	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr7:102105044-102105606	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr7:102102554-102102721	K562	blood:	n/a	chr7:102102649-102102659
34	CHD2	chr7:102111069-102111149	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr7:102107547-102107747	GM12878	blood:	n/a	n/a
36	CHD2	chr7:102104973-102105628	GM12878	blood:	n/a	n/a
37	CHD2	chr7:102104946-102105631	HepG2	liver:	n/a	n/a
38	CHD2	chr7:102105097-102105518	K562	blood:	n/a	n/a
39	CREB1	chr7:102105296-102105555	A549	lung:	n/a	n/a
40	CREB1	chr7:102105108-102105614	A549	lung:	n/a	n/a
41	CREB1	chr7:102105174-102105661	ECC-1	luminal epithelium:	n/a	n/a
42	CREB1	chr7:102104730-102105812	HepG2	liver:	n/a	n/a
43	CTCF	chr7:102105000-102105150	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr7:102107680-102107830	GM12864	blood:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
45	CTCF	chr7:102107360-102107510	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr7:102105480-102105630	GM12870	blood:	n/a	n/a
47	CTCF	chr7:102105440-102105590	GM06990	blood:	n/a	n/a
48	CTCF	chr7:102111070-102111165	Gliobla	brain:	n/a	n/a
49	CTCF	chr7:102105249-102105662	K562	blood:	n/a	chr7:102105413-102105426
50	CTCF	chr7:102107960-102108110	AoAF	blood vessel:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102104807-102104857	GM12892	blood:	n/a
2	chr7:102105256-102105306	K562	blood:	n/a
3	chr7:102105781-102105831	HCM	heart:	n/a
4	chr7:102105781-102105831	NHBE	bronchial:	n/a
5	chr7:102105256-102105306	A549	lung:	n/a
6	chr7:102104807-102104857	HCM	heart:	n/a
7	chr7:102104916-102104966	GM12891	blood:	n/a
8	chr7:102109095-102109145	Hela-S3	cervix:	n/a
9	chr7:102104916-102104966	AG09319	gingival:	n/a
10	chr7:102104297-102104347	HCF	heart:	n/a
11	chr7:102105124-102105174	Jurkat	blood:	n/a
12	chr7:102105195-102105245	HAEpiC	amniotic membrane:	n/a
13	chr7:102105641-102105691	AG04449	skin:	fetal
14	chr7:102102804-102102854	MCF-7	breast:	n/a
15	chr7:102104916-102104966	NHDF-neo	bronchial:	n/a
16	chr7:102105124-102105174	ECC-1	luminal epithelium:	n/a
17	chr7:102109446-102109496	HRE	kidney:	n/a
18	chr7:102104916-102104966	PFSK-1	brain:	n/a
19	chr7:102104916-102104966	HRE	kidney:	n/a
20	chr7:102107737-102107787	MCF-7	breast:	n/a
21	chr7:102105124-102105174	HMEC	breast:	n/a
22	chr7:102105753-102105803	LNCaP	prostate:	n/a
23	chr7:102105201-102105251	BJ	skin:	n/a
24	chr7:102105124-102105174	NB4	blood:	n/a
25	chr7:102105124-102105174	HNPCEpiC	eye:	n/a
26	chr7:102107737-102107787	HUVEC	blood vessel:	n/a
27	chr7:102105344-102105394	RPTEC	kidney:	n/a
28	chr7:102109446-102109496	PrEC	prostate:	n/a
29	chr7:102105753-102105803	HRCEpiC	kidney:	n/a
30	chr7:102102804-102102854	H1-hESC	embryonic stem cell:	embryo
31	chr7:102105753-102105803	PANC-1	pancreas:	n/a
32	chr7:102109247-102109297	HPAEpiC	pulmonary alveolar:	n/a
33	chr7:102105195-102105245	IMR90	lung:	fetal
34	chr7:102104297-102104347	CMK	blood:	n/a
35	chr7:102105201-102105251	BE2_C	brain:	n/a
36	chr7:102104297-102104347	GM06990	blood:	n/a
37	chr7:102105195-102105245	AG09319	gingival:	n/a
38	chr7:102105753-102105803	CMK	blood:	n/a
39	chr7:102105256-102105306	AG09309	skin:	n/a
40	chr7:102105641-102105691	SK-N-MC	brain:	n/a
41	chr7:102109095-102109145	NH-A	brain:	n/a
42	chr7:102104916-102104966	PANC-1	pancreas:	n/a
43	chr7:102105205-102105255	Hela-S3	cervix:	n/a
44	chr7:102109446-102109496	GM12892	blood:	n/a
45	chr7:102105753-102105803	NHDF-neo	bronchial:	n/a
46	chr7:102105781-102105831	SAEC	small airway:	n/a
47	chr7:102105344-102105394	PANC-1	pancreas:	n/a
48	chr7:102109095-102109145	GM12891	blood:	n/a
49	chr7:102105256-102105306	LNCaP	prostate:	n/a
50	chr7:102105205-102105255	NT2-D1	testis:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:102085730..102086410-chr7:102110585..102111557,2	K562	blood:
2	chr7:102074336..102076927-chr7:102105688..102108273,2	K562	blood:
3	chr7:102100941..102102997-chr7:102104685..102106440,2	MCF-7	breast:
4	chr7:101935058..101937626-chr7:102103527..102105838,2	MCF-7	breast:
5	chr10:12391000..12393664-chr7:102102754..102105293,2	MCF-7	breast:
6	chr7:101929851..101931493-chr7:102106221..102107741,2	MCF-7	breast:
7	chr7:102110628..102112535-chr8:144951000..144953117,2	MCF-7	breast:
8	chr7:102092377..102094022-chr7:102102863..102104706,2	K562	blood:
9	chr7:102073875..102075484-chr7:102103725..102106348,2	MCF-7	breast:
10	chr16:90039038..90039558-chr7:102105289..102105810,2	Hela-S3	cervix:
11	chr6:82462024..82463020-chr7:102105257..102105953,2	NB4	blood:
12	chr7:102096270..102098685-chr7:102100293..102102957,2	K562	blood:
13	chr7:102035604..102038403-chr7:102105375..102107150,2	K562	blood:
14	chr7:102110592..102113197-chr7:102117853..102119354,2	MCF-7	breast:
15	chr7:102073812..102076569-chr7:102099712..102102534,2	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5090	chr7:102106199-102106221	MIMAT0021082

No data

Variant related genes	Relation type
MIR5090	TF binding region
MIR4467	TF binding region
LRWD1	TF binding region
ALKBH4	TF binding region
MIR5090	CpG island
MIR4467	CpG island
LRWD1	CpG island
ALKBH4	CpG island
ENSG00000227184	chromatin interactions
ENSG00000112773	chromatin interactions
ENSG00000264675	chromatin interactions
ENSG00000239480	chromatin interactions
ENSG00000183049	chromatin interactions
ENSG00000128563	chromatin interactions
ENSG00000160993	chromatin interactions
ENSG00000160991	chromatin interactions
ENSG00000223959	chromatin interactions
ENSG00000266715	chromatin interactions
ENSG00000005075	chromatin interactions
ENSG00000161036	chromatin interactions

Extended variants
information (count: 519 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:519 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11764446	chr7:102102343-102102344	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576316183	chr7:102102355-102102356	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs77682035	chr7:102102401-102102402	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs138583075	chr7:102102406-102102407	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs570878730	chr7:102102411-102102412	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs534797896	chr7:102102433-102102434	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs561792552	chr7:102102435-102102436	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs553366053	chr7:102102455-102102456	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs191146696	chr7:102102517-102102518	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs184070575	chr7:102102518-102102519	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs557650786	chr7:102102540-102102541	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs188383377	chr7:102102550-102102551	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs576962641	chr7:102102551-102102552	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs546370323	chr7:102102574-102102575	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs77848122	chr7:102102590-102102591	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs528234284	chr7:102102598-102102599	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs141593538	chr7:102102624-102102625	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs561753237	chr7:102102659-102102660	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs528831774	chr7:102102674-102102675	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs80171221	chr7:102102718-102102719	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs144498807	chr7:102102753-102102754	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs112807070	chr7:102102763-102102764	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs73712495	chr7:102102771-102102772	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs34567475	chr7:102102787-102102788	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs551201599	chr7:102102805-102102806	Weak transcription Genic enhancers Strong transcription Enhancers	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs182138148	chr7:102102815-102102816	Weak transcription Genic enhancers Strong transcription Enhancers	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs113479086	chr7:102102821-102102822	Weak transcription Genic enhancers Strong transcription Enhancers	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs535145432	chr7:102102848-102102849	Weak transcription Genic enhancers Strong transcription Enhancers	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs148396021	chr7:102102877-102102878	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs141638795	chr7:102102999-102103000	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs113720496	chr7:102103031-102103032	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs371913702	chr7:102103038-102103039	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs150585334	chr7:102103163-102103164	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs546513299	chr7:102103188-102103189	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs202153951	chr7:102103207-102103208	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs115160515	chr7:102103265-102103266	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs185156003	chr7:102103292-102103293	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs6465866	chr7:102103293-102103294	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs56208004	chr7:102103294-102103295	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs528868745	chr7:102103372-102103373	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs543759108	chr7:102103382-102103383	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs190744817	chr7:102103386-102103387	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs370280641	chr7:102103403-102103404	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs78507302	chr7:102103415-102103416	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs79075886	chr7:102103421-102103422	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs75836400	chr7:102103423-102103424	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs527258028	chr7:102103514-102103515	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs182024783	chr7:102103610-102103611	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs548992938	chr7:102103673-102103674	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs567302374	chr7:102103682-102103683	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	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
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Cancer	19907438	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1021 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102075000-102104000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr7:102075200-102104200	Weak transcription	Fetal Kidney	kidney
3	chr7:102075600-102103400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr7:102075800-102103600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr7:102076000-102104200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr7:102081200-102104200	Weak transcription	Right Atrium	heart
7	chr7:102084400-102104000	Weak transcription	Fetal Brain Male	brain
8	chr7:102088200-102104200	Weak transcription	HUVEC	blood vessel
9	chr7:102088400-102104000	Weak transcription	Primary hematopoietic stem cells	blood
10	chr7:102092400-102104200	Weak transcription	Psoas Muscle	Psoas
11	chr7:102092400-102104200	Weak transcription	Stomach Mucosa	stomach
12	chr7:102092400-102104200	Weak transcription	A549	lung
13	chr7:102092400-102104200	Weak transcription	HSMM	muscle
14	chr7:102092400-102104200	Weak transcription	NHDF-Ad	bronchial
15	chr7:102092600-102104000	Weak transcription	HSMMtube	muscle
16	chr7:102092600-102104200	Weak transcription	HMEC	breast
17	chr7:102092600-102104200	Weak transcription	NHEK	skin
18	chr7:102093800-102102800	Strong transcription	Fetal Intestine Small	intestine
19	chr7:102094800-102103400	Strong transcription	Fetal Stomach	stomach
20	chr7:102095200-102103400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr7:102095600-102102600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr7:102095600-102102600	Strong transcription	Cortex derived primary cultured neurospheres	brain
23	chr7:102097800-102104000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr7:102097800-102104200	Weak transcription	NH-A	brain
25	chr7:102098400-102104000	Weak transcription	GM12878-XiMat	blood
26	chr7:102098600-102104200	Weak transcription	Hela-S3	cervix
27	chr7:102098800-102104000	Weak transcription	Colon Smooth Muscle	Colon
28	chr7:102098800-102104200	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr7:102098800-102104200	Weak transcription	Colonic Mucosa	Colon
30	chr7:102098800-102104200	Weak transcription	K562	blood
31	chr7:102098800-102104400	Weak transcription	Small Intestine	intestine
32	chr7:102099000-102104000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr7:102099000-102104200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr7:102099000-102104200	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr7:102099000-102104200	Weak transcription	Primary B cells from cord blood	blood
36	chr7:102099000-102104200	Weak transcription	NHLF	lung
37	chr7:102099200-102104000	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr7:102099200-102104000	Weak transcription	HepG2	liver
39	chr7:102099400-102104200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
40	chr7:102099600-102104200	Weak transcription	Osteobl	bone
41	chr7:102100000-102103200	Weak transcription	Brain Anterior Caudate	brain
42	chr7:102100000-102104000	Weak transcription	Primary B cells from peripheral blood	blood
43	chr7:102100000-102104000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr7:102100000-102104000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr7:102100000-102104000	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr7:102100000-102104000	Weak transcription	Pancreas	Pancrea
47	chr7:102100000-102104200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr7:102100000-102104200	Weak transcription	Brain Angular Gyrus	brain
49	chr7:102100000-102104200	Weak transcription	Brain Substantia Nigra	brain
50	chr7:102100000-102104200	Weak transcription	Rectal Mucosa Donor 31	rectum

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