Variant report

Variant	nsv470009
Chromosome Location	chr4:8015421-8085174
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:850)
CpG islands
(count:1775)
Chromatin interactive
region (count:33)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:850 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:8052351-8052437	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr4:8083478-8083876	GM12878	blood:	n/a	n/a
3	BCL3	chr4:8051760-8052130	GM12878	blood:	n/a	n/a
4	BCL3	chr4:8048544-8049032	GM12878	blood:	n/a	chr4:8049002-8049011
5	BCL3	chr4:8029949-8030517	GM12878	blood:	n/a	n/a
6	BCL3	chr4:8081299-8081650	GM12878	blood:	n/a	n/a
7	BCL3	chr4:8081328-8081624	GM12878	blood:	n/a	n/a
8	BCL3	chr4:8029834-8030570	GM12878	blood:	n/a	n/a
9	BCL3	chr4:8051772-8052024	GM12878	blood:	n/a	n/a
10	BCL3	chr4:8083394-8083848	GM12878	blood:	n/a	n/a
11	BCL3	chr4:8039082-8039561	GM12878	blood:	n/a	n/a
12	BCL3	chr4:8048580-8049026	GM12878	blood:	n/a	chr4:8049002-8049011
13	BCL3	chr4:8038912-8039504	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:8023606-8023917	A549	lung:	n/a	chr4:8023761-8023770 chr4:8023761-8023770 chr4:8023762-8023771
15	BHLHE40	chr4:8080025-8080049	K562	blood:	n/a	n/a
16	BHLHE40	chr4:8023530-8024019	HepG2	liver:	n/a	chr4:8023761-8023770 chr4:8023761-8023770 chr4:8023762-8023771
17	BHLHE40	chr4:8023583-8023853	HepG2	liver:	n/a	chr4:8023761-8023770 chr4:8023761-8023770 chr4:8023762-8023771
18	BHLHE40	chr4:8052473-8052834	HepG2	liver:	n/a	n/a
19	BHLHE40	chr4:8023654-8023855	HepG2	liver:	n/a	chr4:8023761-8023770 chr4:8023761-8023770 chr4:8023762-8023771
20	BHLHE40	chr4:8069388-8069707	K562	blood:	n/a	n/a
21	BHLHE40	chr4:8023560-8023959	K562	blood:	n/a	chr4:8023761-8023770 chr4:8023761-8023770 chr4:8023762-8023771
22	BHLHE40	chr4:8083635-8083826	K562	blood:	n/a	n/a
23	BHLHE40	chr4:8080566-8081051	K562	blood:	n/a	n/a
24	BHLHE40	chr4:8042424-8042710	K562	blood:	n/a	n/a
25	BHLHE40	chr4:8052547-8052963	HepG2	liver:	n/a	n/a
26	BHLHE40	chr4:8042425-8042692	HepG2	liver:	n/a	n/a
27	BRCA1	chr4:8030194-8030478	H1-hESC	embryonic stem cell:	n/a	n/a
28	CBX3	chr4:8065639-8066235	HCT-116	colon:	n/a	n/a
29	CBX3	chr4:8065744-8066192	HCT-116	colon:	n/a	n/a
30	CBX3	chr4:8065798-8065980	K562	blood:	n/a	n/a
31	CBX3	chr4:8065778-8066062	K562	blood:	n/a	n/a
32	CEBPB	chr4:8055589-8055789	HepG2	liver:	n/a	n/a
33	CEBPB	chr4:8081951-8082124	HepG2	liver:	n/a	chr4:8082008-8082021
34	CEBPB	chr4:8058752-8058940	HepG2	liver:	n/a	chr4:8058881-8058892
35	CEBPB	chr4:8058783-8058947	HepG2	liver:	n/a	chr4:8058881-8058892
36	CEBPB	chr4:8034949-8035108	HepG2	liver:	n/a	n/a
37	CEBPB	chr4:8081899-8082151	H1-hESC	embryonic stem cell:	n/a	chr4:8082008-8082021
38	CEBPD	chr4:8052511-8052966	HepG2	liver:	n/a	n/a
39	CHD2	chr4:8049980-8049988	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr4:8060181-8060187	HepG2	liver:	n/a	n/a
41	CHD2	chr4:8052164-8052523	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr4:8051122-8051443	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr4:8048823-8048827	GM12878	blood:	n/a	n/a
44	CHD2	chr4:8083583-8083726	GM12878	blood:	n/a	n/a
45	CTCF	chr4:8017380-8017530	Caco-2	colon:	n/a	chr4:8017452-8017468 chr4:8017454-8017464 chr4:8017446-8017467 chr4:8017451-8017469
46	CTCF	chr4:8023632-8023814	K562	blood:	n/a	chr4:8023721-8023730 chr4:8023720-8023733 chr4:8023710-8023731 chr4:8023716-8023732 chr4:8023715-8023733 chr4:8023730-8023743 chr4:8023717-8023730
47	CTCF	chr4:8017384-8017387	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr4:8023441-8024007	A549	lung:	n/a	chr4:8023721-8023730 chr4:8023720-8023733 chr4:8023710-8023731 chr4:8023716-8023732 chr4:8023715-8023733 chr4:8023730-8023743 chr4:8023717-8023730
49	CTCF	chr4:8017400-8017550	SK-N-SH_RA	brain:	n/a	chr4:8017452-8017468 chr4:8017454-8017464 chr4:8017446-8017467 chr4:8017451-8017469
50	CTCF	chr4:8017440-8017590	HCM	heart:	n/a	chr4:8017452-8017468 chr4:8017454-8017464 chr4:8017446-8017467 chr4:8017451-8017469

(count:1775 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8025157-8025207	Hela-S3	cervix:	n/a
2	chr4:8023314-8023364	GM19239	blood:	n/a
3	chr4:8081109-8081159	AoSMC	blood vessel:	n/a
4	chr4:8073804-8073854	CMK	blood:	n/a
5	chr4:8073804-8073854	SK-N-SH	brain:	n/a
6	chr4:8022071-8022121	SKMC	muscle:	n/a
7	chr4:8025157-8025207	Hela-S3	cervix:	n/a
8	chr4:8023314-8023364	GM19239	blood:	n/a
9	chr4:8081109-8081159	AoSMC	blood vessel:	n/a
10	chr4:8073804-8073854	CMK	blood:	n/a
11	chr4:8073804-8073854	SK-N-SH	brain:	n/a
12	chr4:8022071-8022121	SKMC	muscle:	n/a
13	chr4:8022071-8022121	HUVEC	blood vessel:	n/a
14	chr4:8084145-8084195	HRPEpiC	eye:	n/a
15	chr4:8022647-8022697	HRE	kidney:	n/a
16	chr4:8034335-8034385	NT2-D1	testis:	n/a
17	chr4:8023314-8023364	NT2-D1	testis:	n/a
18	chr4:8081226-8081276	BE2_C	brain:	n/a
19	chr4:8025157-8025207	NHDF-neo	bronchial:	n/a
20	chr4:8034335-8034385	AG04450	lung:	fetal
21	chr4:8074192-8074242	SK-N-SH_RA	brain:	n/a
22	chr4:8034100-8034150	Jurkat	blood:	n/a
23	chr4:8071003-8071053	GM12891	blood:	n/a
24	chr4:8084145-8084195	HNPCEpiC	eye:	n/a
25	chr4:8023314-8023364	NB4	blood:	n/a
26	chr4:8034335-8034385	RPTEC	kidney:	n/a
27	chr4:8073790-8073840	BJ	skin:	n/a
28	chr4:8022647-8022697	HNPCEpiC	eye:	n/a
29	chr4:8071202-8071252	HRPEpiC	eye:	n/a
30	chr4:8082084-8082134	SK-N-SH_RA	brain:	n/a
31	chr4:8022071-8022121	NH-A	brain:	n/a
32	chr4:8034100-8034150	GM12891	blood:	n/a
33	chr4:8081484-8081534	Jurkat	blood:	n/a
34	chr4:8050781-8050831	HEK293	kidney:	embryo
35	chr4:8073790-8073840	HUVEC	blood vessel:	n/a
36	chr4:8037325-8037375	HPAEpiC	pulmonary alveolar:	n/a
37	chr4:8074092-8074142	HUVEC	blood vessel:	n/a
38	chr4:8071003-8071053	K562	blood:	n/a
39	chr4:8025039-8025089	HUVEC	blood vessel:	n/a
40	chr4:8062590-8062640	A549	lung:	n/a
41	chr4:8023314-8023364	GM12892	blood:	n/a
42	chr4:8074192-8074242	Caco-2	colon:	n/a
43	chr4:8074092-8074142	HL-60	blood:	n/a
44	chr4:8023314-8023364	T-47D	breast:	n/a
45	chr4:8071003-8071053	HRE	kidney:	n/a
46	chr4:8022647-8022697	ovcar-3	ovarian:	n/a
47	chr4:8074092-8074142	GM19239	blood:	n/a
48	chr4:8034100-8034150	AG10803	skin:	n/a
49	chr4:8073790-8073840	SKMC	muscle:	n/a
50	chr4:8062478-8062528	Hepatocyte	liver:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:8034679..8036492-chr4:8044258..8047037,2	K562	blood:
2	chr4:8020577..8022876-chr4:8022955..8025277,2	MCF-7	breast:
3	chr4:8072811..8078672-chr4:8079425..8083106,5	MCF-7	breast:
4	chr4:8034679..8036492-chr4:8044258..8047037,2	K562	blood:
5	chr4:8030886..8034532-chr4:8039153..8041983,3	MCF-7	breast:
6	chr4:8048107..8050691-chr4:8051962..8053661,2	K562	blood:
7	chr4:8055317..8057478-chr4:8062900..8065450,3	MCF-7	breast:
8	chr4:8039157..8040706-chr4:8050002..8052437,2	K562	blood:
9	chr4:8030441..8032567-chr4:8033404..8037009,3	K562	blood:
10	chr4:8027811..8029629-chr4:8031244..8032843,2	K562	blood:
11	chr4:8039157..8040706-chr4:8050002..8052437,2	K562	blood:
12	chr4:8021662..8023195-chr4:8024850..8026832,2	K562	blood:
13	chr4:8019333..8020892-chr4:8033325..8035259,2	MCF-7	breast:
14	chr4:8019333..8020892-chr4:8033325..8035259,2	MCF-7	breast:
15	chr4:8019469..8024052-chr4:8025659..8029825,5	MCF-7	breast:
16	chr4:8030441..8032567-chr4:8033404..8037009,3	K562	blood:
17	chr4:8030886..8034532-chr4:8039153..8041983,3	MCF-7	breast:
18	chr4:8073521..8075555-chr4:8076580..8078200,2	MCF-7	breast:
19	chr4:8033575..8035551-chr4:8063220..8065289,2	K562	blood:
20	chr4:8021380..8023890-chr4:8026077..8027621,2	MCF-7	breast:
21	chr4:8020482..8023593-chr4:8027718..8031223,3	MCF-7	breast:
22	chr4:8020577..8022876-chr4:8022955..8025277,2	MCF-7	breast:
23	chr4:8048107..8050691-chr4:8051962..8053661,2	K562	blood:
24	chr4:8055317..8057478-chr4:8062900..8065450,3	MCF-7	breast:
25	chr4:8005982..8008973-chr4:8021942..8023511,2	MCF-7	breast:
26	chr4:8018368..8020892-chr4:8193998..8196693,2	MCF-7	breast:
27	chr4:8027811..8029629-chr4:8031244..8032843,2	K562	blood:
28	chr4:7806581..7808350-chr4:8014117..8016969,2	MCF-7	breast:
29	chr4:8010549..8013610-chr4:8014316..8016404,3	MCF-7	breast:
30	chr4:8024330..8026063-chr4:8034890..8037450,2	MCF-7	breast:
31	chr4:8034585..8036214-chr4:8037779..8039313,2	MCF-7	breast:
32	chr4:8034585..8036214-chr4:8037779..8039313,2	MCF-7	breast:
33	chr4:8033575..8035551-chr4:8063220..8065289,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH3TC1-2	chr4:8068787-8069451	ENSG00000251460.1
2	lnc-SH3TC1-2	chr4:8068255-8068448	ENSG00000251460.1
3	lnc-AC097381.1.1-1	chr4:8024392-8024853	ENSG00000273267.1

No data

Variant related genes	Relation type
ABLIM2	TF binding region
ENSG00000273267	TF binding region
ENSG00000251460	TF binding region
ABLIM2	CpG island
ENSG00000273267	CpG island
ENSG00000251460	CpG island
ENSG00000207807	chromatin interactions
ENSG00000273267	chromatin interactions
ENSG00000163995	chromatin interactions

Extended variants
information (count: 3682 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3682 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4696729	chr4:8015421-8015422	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
2	rs577666994	chr4:8015451-8015452	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs538698050	chr4:8015467-8015468	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs80332188	chr4:8015496-8015497	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs572055130	chr4:8015523-8015524	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs575264100	chr4:8015533-8015534	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs374084367	chr4:8015593-8015594	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs545835808	chr4:8015597-8015598	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs111886441	chr4:8015630-8015631	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs561156845	chr4:8015654-8015655	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs190426386	chr4:8015675-8015676	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs562406639	chr4:8015676-8015677	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs543255938	chr4:8015683-8015684	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs183433748	chr4:8015770-8015771	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs532516484	chr4:8015785-8015786	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs547472770	chr4:8015846-8015847	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs10938681	chr4:8015869-8015870	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs148105792	chr4:8015892-8015893	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs548508090	chr4:8015911-8015912	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs570022269	chr4:8015918-8015919	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs537700734	chr4:8015919-8015920	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs552517282	chr4:8015955-8015956	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs371842059	chr4:8015968-8015969	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs16841567	chr4:8015973-8015974	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs553880905	chr4:8015974-8015975	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs568828780	chr4:8015978-8015979	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs536264294	chr4:8015985-8015986	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs554559217	chr4:8016005-8016006	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs141899254	chr4:8016007-8016008	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs146054861	chr4:8016015-8016016	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs533033258	chr4:8016070-8016071	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs576949131	chr4:8016092-8016093	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs541171591	chr4:8016140-8016141	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs76072214	chr4:8016144-8016145	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs113884177	chr4:8016150-8016151	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs576073003	chr4:8016152-8016153	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs530092991	chr4:8016156-8016157	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs16841570	chr4:8016164-8016165	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs533779472	chr4:8016175-8016176	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs143407302	chr4:8016212-8016213	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs372312788	chr4:8016217-8016218	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs112587815	chr4:8016234-8016235	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs187756786	chr4:8016250-8016251	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs528687865	chr4:8016275-8016276	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs368976107	chr4:8016278-8016279	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs78863869	chr4:8016280-8016281	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs541875686	chr4:8016313-8016314	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs73092319	chr4:8016319-8016320	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs536325745	chr4:8016320-8016321	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs140037149	chr4:8016345-8016346	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1123 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8007200-8018000	Weak transcription	Psoas Muscle	Psoas
2	chr4:8007800-8022000	Weak transcription	Esophagus	oesophagus
3	chr4:8010600-8052000	Weak transcription	Left Ventricle	heart
4	chr4:8011200-8018200	Weak transcription	Spleen	Spleen
5	chr4:8012400-8039000	Weak transcription	Gastric	stomach
6	chr4:8012600-8016200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr4:8012800-8017200	Weak transcription	Right Atrium	heart
8	chr4:8012800-8035000	Weak transcription	Pancreas	Pancrea
9	chr4:8013000-8016400	Weak transcription	Brain Anterior Caudate	brain
10	chr4:8013000-8020600	Weak transcription	Brain Angular Gyrus	brain
11	chr4:8013000-8021400	Weak transcription	Fetal Intestine Small	intestine
12	chr4:8013000-8036600	Weak transcription	Right Ventricle	heart
13	chr4:8013200-8017000	Weak transcription	Brain Cingulate Gyrus	brain
14	chr4:8013200-8017000	Weak transcription	Brain Hippocampus Middle	brain
15	chr4:8013200-8017000	Weak transcription	Fetal Heart	heart
16	chr4:8013200-8017200	Weak transcription	Stomach Smooth Muscle	stomach
17	chr4:8013200-8018200	Weak transcription	Fetal Intestine Large	intestine
18	chr4:8013200-8020400	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr4:8013200-8020600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr4:8013400-8017000	Weak transcription	Brain Substantia Nigra	brain
21	chr4:8013400-8017200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr4:8014000-8017200	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr4:8014800-8016000	Enhancers	HepG2	liver
24	chr4:8014800-8031400	Strong transcription	Skeletal Muscle Female	skeletal muscle
25	chr4:8015400-8016400	Strong transcription	Aorta	Aorta
26	chr4:8015400-8018000	Strong transcription	Skeletal Muscle Male	skeletal muscle
27	chr4:8016000-8017000	Weak transcription	HepG2	liver
28	chr4:8016200-8016600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr4:8016400-8016600	Enhancers	Brain Anterior Caudate	brain
30	chr4:8016400-8027400	Weak transcription	Aorta	Aorta
31	chr4:8016600-8017000	Weak transcription	Brain Anterior Caudate	brain
32	chr4:8016600-8021600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr4:8016800-8017400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr4:8017000-8017200	Enhancers	Brain Hippocampus Middle	brain
35	chr4:8017000-8017200	Active TSS	Brain Substantia Nigra	brain
36	chr4:8017000-8017200	Active TSS	HepG2	liver
37	chr4:8017000-8017400	Enhancers	Brain Anterior Caudate	brain
38	chr4:8017000-8017400	Enhancers	Brain Cingulate Gyrus	brain
39	chr4:8017000-8017400	Enhancers	Fetal Heart	heart
40	chr4:8017000-8017400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
41	chr4:8017000-8017400	Enhancers	A549	lung
42	chr4:8017000-8017400	Flanking Bivalent TSS/Enh	Osteobl	bone
43	chr4:8017000-8017600	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr4:8017000-8017600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr4:8017200-8017400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr4:8017200-8017400	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr4:8017200-8017400	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr4:8017200-8017400	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr4:8017200-8017400	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr4:8017200-8017400	Flanking Active TSS	Brain Hippocampus Middle	brain

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