Variant report

Variant	nsv970969
Chromosome Location	chr7:150645769-150655995
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:352)
CpG islands
(count:1282)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:352 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:150655739-150656075	K562	blood:	n/a	n/a
2	ARID3A	chr7:150651289-150651294	K562	blood:	n/a	n/a
3	ARID3A	chr7:150652799-150653200	K562	blood:	n/a	n/a
4	ARID3A	chr7:150653679-150653916	K562	blood:	n/a	n/a
5	BACH1	chr7:150653134-150653352	K562	blood:	n/a	n/a
6	BACH1	chr7:150655692-150655856	K562	blood:	n/a	n/a
7	BCL3	chr7:150648664-150648959	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:150650536-150650752	K562	blood:	n/a	n/a
9	BHLHE40	chr7:150652169-150652227	K562	blood:	n/a	n/a
10	BHLHE40	chr7:150652519-150653469	K562	blood:	n/a	chr7:150653060-150653076 chr7:150653052-150653068 chr7:150653008-150653024
11	BHLHE40	chr7:150651237-150651740	K562	blood:	n/a	n/a
12	BHLHE40	chr7:150655690-150656076	K562	blood:	n/a	n/a
13	CBX3	chr7:150652288-150653627	K562	blood:	n/a	n/a
14	CBX3	chr7:150655569-150656404	K562	blood:	n/a	n/a
15	CBX3	chr7:150652921-150653429	K562	blood:	n/a	n/a
16	CCNT2	chr7:150646201-150646302	K562	blood:	n/a	n/a
17	CCNT2	chr7:150652354-150653743	K562	blood:	n/a	chr7:150653594-150653603 chr7:150652992-150653001 chr7:150653045-150653054 chr7:150652934-150652943
18	CCNT2	chr7:150647892-150648019	K562	blood:	n/a	n/a
19	CCNT2	chr7:150651820-150651983	K562	blood:	n/a	n/a
20	CCNT2	chr7:150655484-150655659	K562	blood:	n/a	n/a
21	CEBPB	chr7:150655812-150656012	K562	blood:	n/a	n/a
22	CEBPB	chr7:150652922-150653267	K562	blood:	n/a	n/a
23	CEBPB	chr7:150654415-150654679	K562	blood:	n/a	n/a
24	CEBPD	chr7:150652795-150653498	K562	blood:	n/a	n/a
25	CHD2	chr7:150651973-150652349	K562	blood:	n/a	n/a
26	CHD2	chr7:150655838-150656041	K562	blood:	n/a	n/a
27	CHD2	chr7:150652674-150653368	K562	blood:	n/a	n/a
28	CTCF	chr7:150654440-150654590	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr7:150655765-150655931	K562	blood:	n/a	n/a
30	CTCF	chr7:150654380-150654857	K562	blood:	n/a	n/a
31	CTCF	chr7:150652740-150652890	SAEC	small airway:	n/a	n/a
32	CTCF	chr7:150647197-150647504	T-47D	breast:	n/a	n/a
33	CTCF	chr7:150652659-150652878	T-47D	breast:	n/a	n/a
34	CTCF	chr7:150647328-150647372	GM12878	blood:	n/a	n/a
35	CTCF	chr7:150652740-150652890	K562	blood:	n/a	n/a
36	CTCF	chr7:150652587-150653272	K562	blood:	n/a	n/a
37	CTCF	chr7:150647344-150647395	GM12892	blood:	n/a	n/a
38	CTCF	chr7:150647322-150647384	GM19239	blood:	n/a	n/a
39	CTCF	chr7:150648056-150648237	T-47D	breast:	n/a	n/a
40	CTCF	chr7:150647300-150647450	BE2_C	brain:	n/a	n/a
41	CTCF	chr7:150652704-150653326	K562	blood:	n/a	n/a
42	CTCF	chr7:150652660-150652810	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr7:150647360-150647510	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr7:150654518-150654663	K562	blood:	n/a	n/a
45	CTCF	chr7:150647366-150647384	GM12891	blood:	n/a	n/a
46	CTCF	chr7:150647240-150647390	HepG2	liver:	n/a	n/a
47	CTCF	chr7:150647220-150647370	HepG2	liver:	n/a	n/a
48	CTCF	chr7:150648453-150648907	T-47D	breast:	n/a	n/a
49	CTCF	chr7:150654547-150654610	K562	blood:	n/a	n/a
50	CTCF	chr7:150649452-150649726	T-47D	breast:	n/a	n/a

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150653115-150653165	AG09319	gingival:	n/a
2	chr7:150653115-150653165	AG09319	gingival:	n/a
3	chr7:150648283-150648333	RPTEC	kidney:	n/a
4	chr7:150648840-150648890	SK-N-SH_RA	brain:	n/a
5	chr7:150652948-150652998	LNCaP	prostate:	n/a
6	chr7:150655387-150655437	MCF-7	breast:	n/a
7	chr7:150654471-150654521	U87	brain:	n/a
8	chr7:150651937-150651987	HAEpiC	amniotic membrane:	n/a
9	chr7:150655109-150655159	HEK293	kidney:	embryo
10	chr7:150652948-150652998	BE2_C	brain:	n/a
11	chr7:150651937-150651987	HCPEpiC	choroid plexus:	n/a
12	chr7:150653001-150653051	BJ	skin:	n/a
13	chr7:150653001-150653051	HNPCEpiC	eye:	n/a
14	chr7:150652864-150652914	GM19239	blood:	n/a
15	chr7:150654471-150654521	NHDF-neo	bronchial:	n/a
16	chr7:150653195-150653245	HEEpiC	esophagus:	n/a
17	chr7:150649807-150649857	ProgFib	skin:	n/a
18	chr7:150649807-150649857	ovcar-3	ovarian:	n/a
19	chr7:150652702-150652752	Hepatocyte	liver:	n/a
20	chr7:150652864-150652914	BE2_C	brain:	n/a
21	chr7:150653001-150653051	ECC-1	luminal epithelium:	n/a
22	chr7:150653079-150653129	HMEC	breast:	n/a
23	chr7:150647757-150647807	PFSK-1	brain:	n/a
24	chr7:150652702-150652752	HEEpiC	esophagus:	n/a
25	chr7:150651937-150651987	RPTEC	kidney:	n/a
26	chr7:150655109-150655159	Jurkat	blood:	n/a
27	chr7:150648840-150648890	GM19239	blood:	n/a
28	chr7:150653079-150653129	NH-A	brain:	n/a
29	chr7:150648840-150648890	AG09319	gingival:	n/a
30	chr7:150653115-150653165	NH-A	brain:	n/a
31	chr7:150653115-150653165	AoSMC	blood vessel:	n/a
32	chr7:150655109-150655159	H1-hESC	embryonic stem cell:	embryo
33	chr7:150655387-150655437	HRCEpiC	kidney:	n/a
34	chr7:150648840-150648890	CMK	blood:	n/a
35	chr7:150653001-150653051	HUVEC	blood vessel:	n/a
36	chr7:150646704-150646754	NHDF-neo	bronchial:	n/a
37	chr7:150655133-150655183	HUVEC	blood vessel:	n/a
38	chr7:150651937-150651987	HPAEpiC	pulmonary alveolar:	n/a
39	chr7:150646082-150646132	AG09309	skin:	n/a
40	chr7:150652808-150652858	MCF10A-Er-Src	breast:	n/a
41	chr7:150649655-150649705	BE2_C	brain:	n/a
42	chr7:150648497-150648547	ProgFib	skin:	n/a
43	chr7:150646704-150646754	HMEC	breast:	n/a
44	chr7:150654471-150654521	ovcar-3	ovarian:	n/a
45	chr7:150649807-150649857	PANC-1	pancreas:	n/a
46	chr7:150653079-150653129	NHBE	bronchial:	n/a
47	chr7:150652864-150652914	HRPEpiC	eye:	n/a
48	chr7:150654471-150654521	AG04449	skin:	fetal
49	chr7:150653001-150653051	AG04449	skin:	fetal
50	chr7:150652948-150652998	AG09309	skin:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:150646673..150650094-chr7:150670937..150674779,4	MCF-7	breast:
2	chr7:150642265..150645123-chr7:150653775..150655725,2	MCF-7	breast:
3	chr7:150653312..150655773-chr7:150901970..150904173,2	K562	blood:
4	chr7:150654976..150656696-chr7:150671274..150673215,2	MCF-7	breast:
5	chr7:150543894..150545613-chr7:150648689..150650894,2	K562	blood:
6	chr7:150652621..150654850-chr7:150754233..150756879,2	MCF-7	breast:
7	chr7:150654506..150657037-chr7:150811551..150813776,2	MCF-7	breast:
8	chr7:150647011..150651789-chr7:150652430..150656919,6	MCF-7	breast:
9	chr7:150638034..150640570-chr7:150647564..150649196,2	MCF-7	breast:
10	chr7:150648894..150650627-chr7:150658105..150660939,2	MCF-7	breast:
11	chr7:150654869..150656816-chr7:150670691..150673405,2	MCF-7	breast:
12	chr7:150653093..150655640-chr7:150657394..150660194,2	MCF-7	breast:
13	chr7:150654740..150658307-chr7:150674264..150676481,3	MCF-7	breast:
14	chr4:3444972..3445545-chr7:150654913..150655661,2	MCF-7	breast:
15	chr7:150651843..150653881-chr7:150784068..150785698,2	MCF-7	breast:
16	chr7:150567773..150569879-chr7:150653213..150655593,2	K562	blood:

No data

Variant related genes	Relation type
KCNH2	TF binding region
KCNH2	CpG island
ENSG00000164889	chromatin interactions
ENSG00000055118	chromatin interactions
ENSG00000133612	chromatin interactions
ENSG00000164885	chromatin interactions
ENSG00000183016	chromatin interactions

Extended variants
information (count: 730 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:730 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558129096	chr7:150645806-150645807	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs141664034	chr7:150645807-150645808	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577567071	chr7:150645840-150645841	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs543714814	chr7:150645845-150645846	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs563605594	chr7:150645864-150645865	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529469304	chr7:150645890-150645891	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs371624920	chr7:150645909-150645910	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs200451965	chr7:150645933-150645934	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs199473008	chr7:150645945-150645946	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs121912513	chr7:150645954-150645955	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs199473007	chr7:150645955-150645956	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs199473539	chr7:150645963-150645964	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs543184784	chr7:150645989-150645990	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs199473006	chr7:150646000-150646001	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs111531831	chr7:150646001-150646002	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs559217960	chr7:150646008-150646009	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs199473004	chr7:150646026-150646027	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs199473005	chr7:150646027-150646028	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs139295242	chr7:150646028-150646029	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs199473003	chr7:150646033-150646034	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs199473002	chr7:150646059-150646060	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs149367419	chr7:150646061-150646062	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs199473538	chr7:150646069-150646070	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs121912506	chr7:150646072-150646073	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs199473001	chr7:150646078-150646079	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs72549418	chr7:150646082-150646083	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs121912510	chr7:150646083-150646084	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs199473537	chr7:150646084-150646085	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs41311000	chr7:150646088-150646089	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs375147598	chr7:150646091-150646092	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs199473000	chr7:150646119-150646120	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs199472999	chr7:150646122-150646123	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551139237	chr7:150646124-150646125	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs199473536	chr7:150646137-150646138	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572515767	chr7:150646148-150646149	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs371957566	chr7:150646173-150646174	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs201270523	chr7:150646179-150646180	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs147849768	chr7:150646180-150646181	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs376303355	chr7:150646189-150646190	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs530479329	chr7:150646207-150646208	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573180363	chr7:150646214-150646215	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs112681567	chr7:150646217-150646218	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs567543576	chr7:150646235-150646236	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs35355489	chr7:150646258-150646259	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs141482050	chr7:150646260-150646261	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs536482395	chr7:150646264-150646265	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs41314360	chr7:150646270-150646271	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs41307283	chr7:150646281-150646282	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs535122184	chr7:150646283-150646284	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs539403081	chr7:150646325-150646326	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Wilms tumour	21544195	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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150635600-150648000	Weak transcription	Ovary	ovary
2	chr7:150637800-150652400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr7:150639600-150650800	Weak transcription	Pancreas	Pancrea
4	chr7:150639800-150649200	Weak transcription	Gastric	stomach
5	chr7:150640400-150646800	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr7:150640600-150648800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr7:150641800-150649800	Weak transcription	Spleen	Spleen
8	chr7:150642000-150650400	Enhancers	Fetal Heart	heart
9	chr7:150642400-150647200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr7:150643000-150650400	Weak transcription	Fetal Kidney	kidney
11	chr7:150643000-150651800	Weak transcription	HSMMtube	muscle
12	chr7:150643400-150647600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
13	chr7:150643400-150652200	Weak transcription	Brain Angular Gyrus	brain
14	chr7:150643600-150652000	Weak transcription	Brain Cingulate Gyrus	brain
15	chr7:150643600-150652200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr7:150643800-150646600	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr7:150643800-150648000	Weak transcription	Brain Anterior Caudate	brain
18	chr7:150643800-150650800	Weak transcription	Brain Hippocampus Middle	brain
19	chr7:150644000-150647800	Weak transcription	Fetal Brain Female	brain
20	chr7:150644000-150649400	Weak transcription	Rectal Smooth Muscle	rectum
21	chr7:150644000-150649800	Genic enhancers	Stomach Smooth Muscle	stomach
22	chr7:150644200-150646600	Weak transcription	Colon Smooth Muscle	Colon
23	chr7:150644400-150647400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr7:150644600-150645800	Bivalent Enhancer	Fetal Muscle Leg	muscle
25	chr7:150644600-150649200	Weak transcription	Left Ventricle	heart
26	chr7:150644800-150647600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr7:150645000-150646600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr7:150645000-150646800	Genic enhancers	K562	blood
29	chr7:150645000-150647600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr7:150645200-150646000	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr7:150645200-150646200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
32	chr7:150645200-150647400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr7:150645200-150647400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr7:150645200-150651200	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr7:150645400-150645800	Weak transcription	Right Atrium	heart
36	chr7:150645400-150646400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
37	chr7:150645400-150646600	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr7:150645400-150646600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
39	chr7:150645400-150646800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr7:150645400-150647000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
41	chr7:150645400-150647400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr7:150645400-150647600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr7:150645400-150647600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:150645400-150648600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr7:150645400-150651600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr7:150645600-150645800	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
47	chr7:150645600-150645800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
48	chr7:150645600-150645800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
49	chr7:150645600-150645800	Enhancers	Rectal Mucosa Donor 29	rectum
50	chr7:150645600-150646000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell

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