Variant report

Variant	nsv1020950
Chromosome Location	chr7:145683419-146264304
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2030)
CpG islands
(count:1590)
Chromatin interactive
region (count:109)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2030 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:146221753-146221761	K562	blood:	n/a	n/a
2	ARID3A	chr7:145878136-145878188	K562	blood:	n/a	n/a
3	ARID3A	chr7:145787152-145787489	K562	blood:	n/a	n/a
4	ARID3A	chr7:145787264-145787483	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:145755180-145755400	K562	blood:	n/a	n/a
6	ARID3A	chr7:145750569-145750925	K562	blood:	n/a	n/a
7	ARID3A	chr7:145772258-145772458	K562	blood:	n/a	n/a
8	ARID3A	chr7:145703778-145703907	K562	blood:	n/a	n/a
9	ATF1	chr7:145717949-145718148	K562	blood:	n/a	n/a
10	ATF1	chr7:146033922-146034015	K562	blood:	n/a	n/a
11	ATF1	chr7:146124987-146125045	K562	blood:	n/a	n/a
12	ATF1	chr7:146191929-146191962	K562	blood:	n/a	n/a
13	ATF1	chr7:145750609-145750997	K562	blood:	n/a	n/a
14	ATF1	chr7:145775000-145775187	K562	blood:	n/a	n/a
15	ATF1	chr7:145699648-145699984	K562	blood:	n/a	n/a
16	ATF1	chr7:145728285-145728287	K562	blood:	n/a	n/a
17	ATF3	chr7:145750662-145750929	K562	blood:	n/a	n/a
18	ATF3	chr7:145716456-145716610	K562	blood:	n/a	n/a
19	ATF3	chr7:145683356-145683677	K562	blood:	n/a	n/a
20	BACH1	chr7:146022615-146022622	K562	blood:	n/a	n/a
21	BACH1	chr7:145842137-145842377	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr7:145813392-145814179	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr7:146255445-146255494	K562	blood:	n/a	n/a
24	BACH1	chr7:145727177-145727179	K562	blood:	n/a	n/a
25	BACH1	chr7:145686566-145686880	K562	blood:	n/a	n/a
26	BACH1	chr7:145812851-145813178	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr7:145845611-145845615	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr7:145750738-145750913	K562	blood:	n/a	n/a
29	BATF	chr7:146241905-146242175	GM12878	blood:	n/a	chr7:146242043-146242051 chr7:146242071-146242082
30	BATF	chr7:145694359-145694555	GM12878	blood:	n/a	n/a
31	BATF	chr7:145694357-145694559	GM12878	blood:	n/a	n/a
32	BCL11A	chr7:145694365-145694584	GM12878	blood:	n/a	n/a
33	BCL11A	chr7:145694347-145694680	GM12878	blood:	n/a	n/a
34	BHLHE40	chr7:145824603-145824809	K562	blood:	n/a	chr7:145824732-145824741 chr7:145824733-145824742 chr7:145824732-145824741
35	BHLHE40	chr7:145750584-145750950	K562	blood:	n/a	n/a
36	BHLHE40	chr7:145719613-145719737	K562	blood:	n/a	n/a
37	BHLHE40	chr7:145699653-145700059	K562	blood:	n/a	n/a
38	BHLHE40	chr7:145793673-145793674	K562	blood:	n/a	n/a
39	BHLHE40	chr7:145699695-145700051	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:145683463-145683590	K562	blood:	n/a	n/a
41	BHLHE40	chr7:145812888-145813075	K562	blood:	n/a	n/a
42	BHLHE40	chr7:145755118-145755377	K562	blood:	n/a	n/a
43	BHLHE40	chr7:145694345-145694571	HepG2	liver:	n/a	n/a
44	BRCA1	chr7:146220216-146220267	H1-hESC	embryonic stem cell:	n/a	n/a
45	BRCA1	chr7:145787246-145787465	H1-hESC	embryonic stem cell:	n/a	chr7:145787445-145787452
46	BRCA1	chr7:145887640-145887719	GM12878	blood:	n/a	n/a
47	CBX3	chr7:146207215-146207553	K562	blood:	n/a	n/a
48	CBX3	chr7:146207173-146207556	K562	blood:	n/a	n/a
49	CBX3	chr7:145812824-145813236	K562	blood:	n/a	n/a
50	CBX3	chr7:145750559-145750949	K562	blood:	n/a	n/a

(count:1590 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:145875026-145875076	SK-N-SH	brain:	n/a
2	chr7:146019420-146019470	NHBE	bronchial:	n/a
3	chr7:145813421-145813471	T-47D	breast:	n/a
4	chr7:145716504-145716554	GM12892	blood:	n/a
5	chr7:145875026-145875076	SK-N-SH	brain:	n/a
6	chr7:146019420-146019470	NHBE	bronchial:	n/a
7	chr7:145813421-145813471	T-47D	breast:	n/a
8	chr7:145716504-145716554	GM12892	blood:	n/a
9	chr7:145813066-145813116	HPAEpiC	pulmonary alveolar:	n/a
10	chr7:145812842-145812892	LNCaP	prostate:	n/a
11	chr7:145689965-145690015	HUVEC	blood vessel:	n/a
12	chr7:146019420-146019470	U87	brain:	n/a
13	chr7:145689965-145690015	AoSMC	blood vessel:	n/a
14	chr7:145716504-145716554	GM12878	blood:	n/a
15	chr7:145813946-145813996	AG04449	skin:	fetal
16	chr7:145813417-145813467	GM12892	blood:	n/a
17	chr7:145812842-145812892	RPTEC	kidney:	n/a
18	chr7:146130429-146130479	U87	brain:	n/a
19	chr7:145814306-145814356	HUVEC	blood vessel:	n/a
20	chr7:145813915-145813965	HRPEpiC	eye:	n/a
21	chr7:145813915-145813965	Hepatocyte	liver:	n/a
22	chr7:145813413-145813463	NHDF-neo	bronchial:	n/a
23	chr7:145814306-145814356	H1-hESC	embryonic stem cell:	embryo
24	chr7:145812842-145812892	NHDF-neo	bronchial:	n/a
25	chr7:145813915-145813965	SK-N-MC	brain:	n/a
26	chr7:145716504-145716554	IMR90	lung:	fetal
27	chr7:145813439-145813489	HCF	heart:	n/a
28	chr7:145813417-145813467	AG10803	skin:	n/a
29	chr7:145813432-145813482	HCF	heart:	n/a
30	chr7:145945815-145945865	GM12892	blood:	n/a
31	chr7:145813417-145813467	SK-N-SH_RA	brain:	n/a
32	chr7:145716504-145716554	LNCaP	prostate:	n/a
33	chr7:145814152-145814202	HEK293	kidney:	embryo
34	chr7:145813437-145813487	BE2_C	brain:	n/a
35	chr7:145813915-145813965	HCT-116	colon:	n/a
36	chr7:145716504-145716554	HRCEpiC	kidney:	n/a
37	chr7:145814152-145814202	PFSK-1	brain:	n/a
38	chr7:145814306-145814356	GM12878	blood:	n/a
39	chr7:145812842-145812892	HUVEC	blood vessel:	n/a
40	chr7:145812871-145812921	NB4	blood:	n/a
41	chr7:145814306-145814356	ProgFib	skin:	n/a
42	chr7:145813008-145813058	HMEC	breast:	n/a
43	chr7:145813413-145813463	MCF-7	breast:	n/a
44	chr7:146130429-146130479	PrEC	prostate:	n/a
45	chr7:145814152-145814202	HepG2	liver:	n/a
46	chr7:145813008-145813058	K562	blood:	n/a
47	chr7:145813437-145813487	HCPEpiC	choroid plexus:	n/a
48	chr7:145813066-145813116	HUVEC	blood vessel:	n/a
49	chr7:145812842-145812892	GM06990	blood:	n/a
50	chr7:145814003-145814053	BJ	skin:	n/a

(count:109 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:146250194..146253829-chr7:146254649..146256608,3	K562	blood:
2	chr7:146185198..146188114-chr7:146194009..146195927,2	K562	blood:
3	chr7:145709801..145711953-chr7:145718759..145720900,2	K562	blood:
4	chr7:145728196..145729845-chr7:145732878..145734449,2	K562	blood:
5	chr7:144712868..144713384-chr7:145787231..145787880,2	MCF-7	breast:
6	chr7:145771822..145774419-chr7:145775630..145778255,2	K562	blood:
7	chr7:145988038..145989736-chr7:145992431..145994390,2	MCF-7	breast:
8	chr7:145449251..145450121-chr7:145786995..145787798,2	K562	blood:
9	chr7:145716150..145718502-chr7:145724762..145727451,3	K562	blood:
10	chr7:145688129..145689794-chr7:145691841..145693343,2	K562	blood:
11	chr7:146250194..146253829-chr7:146254649..146256608,3	K562	blood:
12	chr7:145872793..145874958-chr7:145879839..145881542,2	K562	blood:
13	chr7:145879679..145882297-chr7:145885152..145887234,2	K562	blood:
14	chr7:145782508..145785032-chr7:145801785..145804184,2	K562	blood:
15	chr7:145950902..145953007-chr7:145958921..145960745,2	K562	blood:
16	chr16:70557427..70557946-chr7:146244932..146245452,2	Hela-S3	cervix:
17	chr7:145691152..145693851-chr7:145700419..145703123,2	K562	blood:
18	chr7:145870161..145872926-chr7:145874663..145877386,2	K562	blood:
19	chr7:145684833..145687404-chr7:145706239..145708972,2	K562	blood:
20	chr7:145697305..145699991-chr7:145700087..145702652,2	K562	blood:
21	chr7:145771822..145774419-chr7:145775630..145778255,2	K562	blood:
22	chr7:146074528..146076132-chr7:146081076..146083881,2	K562	blood:
23	chr7:145749911..145752197-chr7:145756067..145758121,2	K562	blood:
24	chr5:40835299..40835996-chr7:145980649..145981149,2	Hela-S3	cervix:
25	chr7:146077363..146079072-chr7:146098860..146101793,2	K562	blood:
26	chr7:145805690..145807503-chr7:145809091..145811939,2	K562	blood:
27	chr7:145716150..145718866-chr7:145724746..145727382,4	K562	blood:
28	chr7:145721579..145724410-chr7:145727561..145729692,3	K562	blood:
29	chr7:145691152..145693851-chr7:145700419..145703123,2	K562	blood:
30	chr7:145800703..145803223-chr7:145808125..145812343,3	K562	blood:
31	chr7:146077363..146079072-chr7:146098860..146101793,2	K562	blood:
32	chr7:145931221..145934684-chr7:145937680..145940356,3	K562	blood:
33	chr7:145704641..145707485-chr7:145707900..145710506,2	K562	blood:
34	chr7:145721579..145724410-chr7:145727561..145729692,3	K562	blood:
35	chr7:145716150..145718502-chr7:145724762..145727451,3	K562	blood:
36	chr7:145693446..145695856-chr7:145705246..145708235,3	K562	blood:
37	chr7:146077123..146080368-chr7:146083154..146084711,3	K562	blood:
38	chr7:145696018..145698429-chr7:145703495..145706180,2	K562	blood:
39	chr7:145716150..145718866-chr7:145724746..145727382,4	K562	blood:
40	chr7:145715314..145718621-chr7:145718754..145721889,3	K562	blood:
41	chr7:145749911..145752197-chr7:145756067..145758121,2	K562	blood:
42	chr7:145747031..145750592-chr7:145750800..145754125,3	K562	blood:
43	chr7:146143168..146145467-chr7:146146129..146147911,2	MCF-7	breast:
44	chr7:145728196..145729845-chr7:145732878..145734449,2	K562	blood:
45	chr7:145715314..145718621-chr7:145718754..145721889,3	K562	blood:
46	chr7:145988038..145989736-chr7:145992431..145994390,2	MCF-7	breast:
47	chr7:145747031..145750592-chr7:145750800..145754125,3	K562	blood:
48	chr7:145774442..145776114-chr7:145776448..145779399,2	K562	blood:
49	chr7:145697305..145699991-chr7:145700087..145702652,2	K562	blood:
50	chr7:145693446..145695856-chr7:145705246..145708235,3	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNTNAP2-4	chr7:145747160-145747457	NONHSAT123944
2	lnc-CNTNAP2-3	chr7:145747717-145747809	NONHSAT123945
3	lnc-CNTNAP2-3	chr7:145777121-145777289	NONHSAT123945
4	lnc-TPK1-4	chr7:146113435-146113645	NONHSAT123948
5	lnc-CNTNAP2-2	chr7:145793180-145793471	NONHSAT123946

No data

Variant related genes	Relation type
CNTNAP2	TF binding region
RN7SL207P	TF binding region
CNTNAP2	CpG island
RN7SL207P	CpG island
ENSG00000103051	chromatin interactions
ENSG00000174469	chromatin interactions
ENSG00000145592	chromatin interactions
ENSG00000264018	chromatin interactions
ENSG00000189091	chromatin interactions

Extended variants
information (count: 10022 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:10022 , 50 per page) page: 1 2 3 4 5 6 7 ... 201

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559100436	chr7:145683438-145683439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs193045434	chr7:145683443-145683444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141997134	chr7:145683459-145683460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs75157668	chr7:145683498-145683499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs530153874	chr7:145683538-145683539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2177748	chr7:145683594-145683595	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs78464770	chr7:145683655-145683656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs527572702	chr7:145683675-145683676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541979295	chr7:145683763-145683764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs185217798	chr7:145683840-145683841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs77018171	chr7:145683841-145683842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575817109	chr7:145683852-145683853	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543240732	chr7:145683886-145683887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs145715537	chr7:145683898-145683899	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138184597	chr7:145683925-145683926	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs367788145	chr7:145684043-145684044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs535574507	chr7:145684066-145684067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs576736560	chr7:145684072-145684073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs75266345	chr7:145684106-145684107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs78681018	chr7:145684108-145684109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188373257	chr7:145684116-145684117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556980772	chr7:145684118-145684119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs375976437	chr7:145684122-145684123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs62503387	chr7:145684127-145684128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191877762	chr7:145684155-145684156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183585168	chr7:145684171-145684172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577132242	chr7:145684172-145684173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs74706766	chr7:145684179-145684180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188278410	chr7:145684191-145684192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563403003	chr7:145684259-145684260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574576359	chr7:145684307-145684308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs142956377	chr7:145684325-145684326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371710394	chr7:145684326-145684327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541997627	chr7:145684332-145684333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs77061639	chr7:145684397-145684398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs377259745	chr7:145684473-145684474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546189755	chr7:145684481-145684482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187256811	chr7:145684528-145684529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190444333	chr7:145684551-145684552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531662517	chr7:145684624-145684625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552842072	chr7:145684684-145684685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369818136	chr7:145684703-145684704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561900310	chr7:145684719-145684720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181631795	chr7:145684757-145684758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs186765589	chr7:145684774-145684775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565773854	chr7:145684818-145684819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539026835	chr7:145684833-145684834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575520776	chr7:145684838-145684839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540943911	chr7:145684921-145684922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538179588	chr7:145684957-145684958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Splenic marginal zone lymphoma	21957467	CNVD
Glioblastoma multiforme	18628472	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	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pancreatitis	21956041	CNVD
Acute myeloid leukemia	16864856	CNVD
Gastric cancer	16891809	CNVD
Lung cancer	17086460	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20808228	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Neuropsychiatric disorder	21827697	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Autism	20964600	CNVD
Epilepsy	17646849	CNVD
Mental retardation	19896112	CNVD
Autism	20531469	CNVD
Epilepsy	20502679	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:846 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:145682600-145683800	Enhancers	K562	blood
2	chr7:145683000-145683800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr7:145683600-145684000	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr7:145683800-145686800	Weak transcription	K562	blood
5	chr7:145686800-145687000	ZNF genes & repeats	K562	blood
6	chr7:145687000-145694000	Weak transcription	K562	blood
7	chr7:145698800-145700600	Enhancers	Primary hematopoietic stem cells	blood
8	chr7:145699400-145700000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr7:145699400-145700000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr7:145699400-145700400	Enhancers	Primary B cells from peripheral blood	blood
11	chr7:145699400-145700400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr7:145699800-145700400	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr7:145700000-145700200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr7:145700000-145700400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr7:145700200-145700400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr7:145704800-145705200	Enhancers	Fetal Lung	lung
17	chr7:145705000-145705200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr7:145705000-145705200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
19	chr7:145705200-145706200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr7:145706400-145706600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr7:145715200-145715400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr7:145716200-145716800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
23	chr7:145716200-145716800	Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr7:145716200-145717000	Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr7:145716400-145716800	Active TSS	H9 Cell Line	embryonic stem cell
26	chr7:145716400-145716800	Active TSS	K562	blood
27	chr7:145716800-145717000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
28	chr7:145716800-145717000	Flanking Active TSS	K562	blood
29	chr7:145717000-145717200	Active TSS	K562	blood
30	chr7:145717200-145717600	Enhancers	K562	blood
31	chr7:145717600-145722000	Weak transcription	K562	blood
32	chr7:145718600-145719800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr7:145718800-145719400	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr7:145718800-145719600	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr7:145718800-145719600	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr7:145719000-145720200	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr7:145719200-145719600	Enhancers	H1 Cell Line	embryonic stem cell
38	chr7:145749600-145751600	Enhancers	K562	blood
39	chr7:145751600-145754400	Weak transcription	K562	blood
40	chr7:145754400-145755800	Enhancers	K562	blood
41	chr7:145755400-145756400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr7:145759400-145760400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr7:145770200-145770400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr7:145770400-145771200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr7:145771200-145771800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr7:145787400-145788400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr7:145790600-145792400	Enhancers	Fetal Lung	lung
48	chr7:145812000-145812600	Enhancers	Brain Germinal Matrix	brain
49	chr7:145812000-145813600	Active TSS	Brain Inferior Temporal Lobe	brain
50	chr7:145812200-145812600	Enhancers	Fetal Brain Male	brain

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