Variant report

Variant	nsv519971
Chromosome Location	chr3:137782655-137801213
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:137785097-137785621	GM12878	blood:	n/a	n/a
2	ATF2	chr3:137785134-137785566	GM12878	blood:	n/a	n/a
3	ATF3	chr3:137787378-137787793	A549	lung:	n/a	n/a
4	BACH1	chr3:137787433-137787783	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr3:137791661-137791861	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr3:137785253-137785567	GM12878	blood:	n/a	n/a
7	BATF	chr3:137785171-137785600	GM12878	blood:	n/a	n/a
8	BCL11A	chr3:137785184-137785605	GM12878	blood:	n/a	n/a
9	BCL3	chr3:137797771-137798329	A549	lung:	n/a	n/a
10	BHLHE40	chr3:137787441-137787777	GM12878	blood:	n/a	chr3:137787472-137787488
11	BHLHE40	chr3:137787456-137787761	K562	blood:	n/a	chr3:137787472-137787488
12	BRCA1	chr3:137798000-137798310	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr3:137787458-137787700	HepG2	liver:	n/a	n/a
14	CEBPB	chr3:137787485-137787727	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr3:137797730-137798314	A549	lung:	n/a	n/a
16	CEBPB	chr3:137796946-137797290	IMR90	lung:	n/a	chr3:137797112-137797124
17	CEBPB	chr3:137797865-137798275	MCF-7	breast:	n/a	n/a
18	CEBPB	chr3:137796967-137797295	A549	lung:	n/a	chr3:137797112-137797124
19	CEBPB	chr3:137797891-137798249	A549	lung:	n/a	n/a
20	CEBPB	chr3:137800574-137802165	IMR90	lung:	n/a	chr3:137801266-137801278
21	CEBPB	chr3:137797808-137798324	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr3:137797630-137798331	IMR90	lung:	n/a	n/a
23	CEBPB	chr3:137796965-137797279	A549	lung:	n/a	chr3:137797112-137797124
24	CEBPB	chr3:137797673-137798389	A549	lung:	n/a	n/a
25	CEBPB	chr3:137796837-137797381	A549	lung:	n/a	chr3:137797112-137797124
26	CEBPB	chr3:137797768-137798466	HCT-116	colon:	n/a	n/a
27	CHD1	chr3:137787483-137787730	GM12878	blood:	n/a	n/a
28	CHD2	chr3:137787435-137787776	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr3:137787481-137787754	GM12878	blood:	n/a	n/a
30	CHD2	chr3:137787461-137787792	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr3:137787565-137787755	HepG2	liver:	n/a	n/a
32	CREB1	chr3:137785126-137785627	GM12878	blood:	n/a	n/a
33	CTCF	chr3:137787560-137787710	HRE	kidney:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
34	CTCF	chr3:137787413-137787769	ECC-1	luminal epithelium:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
35	CTCF	chr3:137787438-137787765	GM19239	blood:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
36	CTCF	chr3:137787413-137787806	K562	blood:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
37	CTCF	chr3:137787520-137787670	GM06990	blood:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
38	CTCF	chr3:137787469-137787691	A549	lung:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
39	CTCF	chr3:137787520-137787670	WERI-Rb-1	eye:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
40	CTCF	chr3:137787540-137787690	SAEC	small airway:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
41	CTCF	chr3:137787520-137787670	AG10803	skin:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
42	CTCF	chr3:137787560-137787710	HCT-116	colon:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
43	CTCF	chr3:137787540-137787690	NHDF-neo	bronchial:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
44	CTCF	chr3:137787560-137787710	GM12866	blood:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
45	CTCF	chr3:137787455-137787744	Pancreas_OC	pancreas:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
46	CTCF	chr3:137787540-137787690	BE2_C	brain:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
47	CTCF	chr3:137787560-137787710	NB4	blood:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
48	CTCF	chr3:137787520-137787670	GM12865	blood:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
49	CTCF	chr3:137787500-137787650	AG04450	lung:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620
50	CTCF	chr3:137787540-137787690	GM12866	blood:	n/a	chr3:137787598-137787614 chr3:137787600-137787609 chr3:137787597-137787615 chr3:137787599-137787620

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:137787060-137787110	ProgFib	skin:	n/a
2	chr3:137787060-137787110	LNCaP	prostate:	n/a
3	chr3:137787060-137787110	ProgFib	skin:	n/a
4	chr3:137787060-137787110	LNCaP	prostate:	n/a
5	chr3:137787902-137787952	ECC-1	luminal epithelium:	n/a
6	chr3:137787060-137787110	SKMC	muscle:	n/a
7	chr3:137787902-137787952	Hela-S3	cervix:	n/a
8	chr3:137787902-137787952	Hepatocyte	liver:	n/a
9	chr3:137787902-137787952	AG10803	skin:	n/a
10	chr3:137787060-137787110	HEK293	kidney:	embryo
11	chr3:137787902-137787952	HRE	kidney:	n/a
12	chr3:137787902-137787952	NHBE	bronchial:	n/a
13	chr3:137787060-137787110	U87	brain:	n/a
14	chr3:137787902-137787952	SK-N-SH	brain:	n/a
15	chr3:137787902-137787952	BE2_C	brain:	n/a
16	chr3:137787902-137787952	Jurkat	blood:	n/a
17	chr3:137787902-137787952	U87	brain:	n/a
18	chr3:137787902-137787952	HCPEpiC	choroid plexus:	n/a
19	chr3:137787902-137787952	HNPCEpiC	eye:	n/a
20	chr3:137787902-137787952	ProgFib	skin:	n/a
21	chr3:137787060-137787110	NT2-D1	testis:	n/a
22	chr3:137787060-137787110	Caco-2	colon:	n/a
23	chr3:137787902-137787952	T-47D	breast:	n/a
24	chr3:137787902-137787952	GM19239	blood:	n/a
25	chr3:137787060-137787110	HepG2	liver:	n/a
26	chr3:137787902-137787952	HEEpiC	esophagus:	n/a
27	chr3:137787902-137787952	PrEC	prostate:	n/a
28	chr3:137787060-137787110	GM12892	blood:	n/a
29	chr3:137787060-137787110	BJ	skin:	n/a
30	chr3:137787060-137787110	HMEC	breast:	n/a
31	chr3:137787060-137787110	HPAEpiC	pulmonary alveolar:	n/a
32	chr3:137787902-137787952	NHDF-neo	bronchial:	n/a
33	chr3:137787902-137787952	Caco-2	colon:	n/a
34	chr3:137787060-137787110	HRE	kidney:	n/a
35	chr3:137787060-137787110	GM19239	blood:	n/a
36	chr3:137787060-137787110	SK-N-SH	brain:	n/a
37	chr3:137787060-137787110	Hepatocyte	liver:	n/a
38	chr3:137787060-137787110	NH-A	brain:	n/a
39	chr3:137787060-137787110	HCF	heart:	n/a
40	chr3:137787060-137787110	HUVEC	blood vessel:	n/a
41	chr3:137787902-137787952	ovcar-3	ovarian:	n/a
42	chr3:137787902-137787952	HPAEpiC	pulmonary alveolar:	n/a
43	chr3:137787902-137787952	AG04450	lung:	fetal
44	chr3:137787902-137787952	SK-N-SH_RA	brain:	n/a
45	chr3:137787902-137787952	HCF	heart:	n/a
46	chr3:137787060-137787110	GM12891	blood:	n/a
47	chr3:137787060-137787110	HCM	heart:	n/a
48	chr3:137787060-137787110	PrEC	prostate:	n/a
49	chr3:137787902-137787952	NH-A	brain:	n/a
50	chr3:137787902-137787952	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:137798158..137800063-chr3:137800310..137802167,2	MCF-7	breast:
2	chr3:137787960..137790369-chr3:137798612..137800700,2	K562	blood:
3	chr3:137783065..137785092-chr3:137890925..137893820,2	MCF-7	breast:
4	chr3:137794586..137797372-chr3:137799384..137801141,2	MCF-7	breast:
5	chr3:137797953..137799816-chr3:137805788..137808409,2	MCF-7	breast:
6	chr3:137781336..137783358-chr3:137787171..137788980,2	MCF-7	breast:
7	chr3:137783378..137785801-chr3:137789498..137791513,2	K562	blood:
8	chr3:137796613..137798345-chr3:137800057..137802193,2	MCF-7	breast:
9	chr3:137787348..137788077-chr3:137837494..137838376,4	K562	blood:
10	chr3:137787211..137788408-chr3:137837411..137838466,26	MCF-7	breast:
11	chr3:137748327..137751099-chr3:137781297..137783702,2	MCF-7	breast:
12	chr3:137789176..137789822-chr3:137837460..137838165,2	MCF-7	breast:
13	chr3:137780995..137783087-chr3:137786062..137788578,2	MCF-7	breast:
14	chr3:137786807..137788879-chr3:137836537..137838505,22	MCF-7	breast:
15	chr3:137779026..137781498-chr3:137783755..137785265,2	K562	blood:
16	chr3:137776797..137779428-chr3:137782269..137783995,2	MCF-7	breast:
17	chr3:137787960..137791501-chr3:137797864..137801137,4	K562	blood:
18	chr3:137795070..137797856-chr3:137805408..137807844,2	K562	blood:
19	chr3:137781336..137783358-chr3:137787171..137788980,2	MCF-7	breast:
20	chr3:137798306..137800637-chr3:137905206..137907659,2	MCF-7	breast:
21	chr3:137787702..137789743-chr3:137892211..137893755,2	MCF-7	breast:
22	chr3:137787535..137788103-chr3:138634909..138635442,2	K562	blood:
23	chr3:137795704..137798653-chr3:137818142..137820266,2	K562	blood:
24	chr12:90428505..90430564-chr3:137781378..137783907,2	MCF-7	breast:
25	chr3:137783378..137785801-chr3:137789498..137791513,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-A4GNT-3	chr3:137799191-137799462	NONHSAT092319
2	lnc-A4GNT-3	chr3:137800576-137800671	NONHSAT092319

Variant related genes	Relation type
DZIP1L	TF binding region
DZIP1L	CpG island
ENSG00000158163	chromatin interactions
ENSG00000114098	chromatin interactions
ENSG00000138231	chromatin interactions

Extended variants
information (count: 740 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:740 , 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	rs329391	chr3:137782655-137782656	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531638324	chr3:137782786-137782787	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs566453991	chr3:137782897-137782898	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs530307775	chr3:137782923-137782924	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs373173448	chr3:137782962-137782963	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs535524837	chr3:137783003-137783004	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs114923992	chr3:137783020-137783021	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs143606709	chr3:137783037-137783038	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs550529416	chr3:137783065-137783066	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs115586564	chr3:137783071-137783072	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs55984301	chr3:137783116-137783117	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs370775817	chr3:137783125-137783126	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs577470007	chr3:137783146-137783147	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs570344599	chr3:137783147-137783148	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs532814266	chr3:137783151-137783152	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs536447119	chr3:137783180-137783181	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs552306274	chr3:137783192-137783193	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs540049259	chr3:137783203-137783204	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs566025567	chr3:137783264-137783265	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs553544306	chr3:137783269-137783270	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs148022296	chr3:137783293-137783294	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs114750068	chr3:137783331-137783332	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs561974708	chr3:137783350-137783351	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs116526849	chr3:137783411-137783412	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs544589728	chr3:137783423-137783424	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs202221589	chr3:137783460-137783461	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs374741388	chr3:137783489-137783490	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs533624679	chr3:137783517-137783518	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs201438371	chr3:137783547-137783548	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs2199948	chr3:137783548-137783549	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs34517099	chr3:137783565-137783566	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs547254982	chr3:137783572-137783573	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs148421355	chr3:137783580-137783581	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs200415644	chr3:137783594-137783595	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs369063453	chr3:137783601-137783602	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs201136566	chr3:137783616-137783617	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs199666233	chr3:137783619-137783620	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs376372270	chr3:137783641-137783642	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs179282	chr3:137783700-137783701	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs113666615	chr3:137783719-137783720	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs568822760	chr3:137783726-137783727	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs1384588	chr3:137783736-137783737	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs537468587	chr3:137783861-137783862	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs190643290	chr3:137783879-137783880	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs182871016	chr3:137783884-137783885	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs533835063	chr3:137783896-137783897	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs553715759	chr3:137783905-137783906	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs573764118	chr3:137784019-137784020	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs542423623	chr3:137784021-137784022	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs141746664	chr3:137784056-137784057	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Schizophrenia	18511947	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
abnormal development	18461090	CNVD

Chromatin state (count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:137744400-137792000	Weak transcription	Fetal Kidney	kidney
2	chr3:137754400-137783000	Weak transcription	Stomach Mucosa	stomach
3	chr3:137763000-137797600	Weak transcription	Hela-S3	cervix
4	chr3:137766800-137783600	Weak transcription	Brain Substantia Nigra	brain
5	chr3:137767000-137782800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr3:137767200-137791800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr3:137768200-137782800	Weak transcription	Esophagus	oesophagus
8	chr3:137768200-137787600	Weak transcription	A549	lung
9	chr3:137768600-137783600	Weak transcription	Pancreas	Pancrea
10	chr3:137769800-137785600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr3:137770200-137783600	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr3:137770400-137783600	Weak transcription	Fetal Lung	lung
13	chr3:137772800-137792200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:137777800-137790000	Weak transcription	Brain Germinal Matrix	brain
15	chr3:137778200-137800600	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr3:137778400-137787400	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr3:137778600-137787600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr3:137778800-137800400	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr3:137779200-137783000	Weak transcription	Colonic Mucosa	Colon
20	chr3:137779200-137792400	Strong transcription	Fetal Stomach	stomach
21	chr3:137779600-137782800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr3:137779600-137787600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr3:137779800-137787400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr3:137779800-137787600	Strong transcription	Adipose Nuclei	Adipose
25	chr3:137780000-137783800	Strong transcription	Spleen	Spleen
26	chr3:137780000-137784000	Strong transcription	Ovary	ovary
27	chr3:137780000-137785800	Strong transcription	HUES48 Cell Line	embryonic stem cell
28	chr3:137780000-137787200	Strong transcription	Aorta	Aorta
29	chr3:137780000-137792600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr3:137780000-137792600	Strong transcription	Fetal Muscle Trunk	muscle
31	chr3:137780000-137797600	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr3:137780000-137813400	Weak transcription	HUVEC	blood vessel
33	chr3:137780200-137783200	Strong transcription	Pancreatic Islets	Pancreatic Islet
34	chr3:137780200-137786400	Strong transcription	HUES6 Cell Line	embryonic stem cell
35	chr3:137780200-137787600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr3:137780400-137786600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr3:137780400-137787200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr3:137780400-137787400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr3:137780400-137787600	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr3:137780400-137792400	Strong transcription	Stomach Smooth Muscle	stomach
41	chr3:137780600-137784600	Weak transcription	GM12878-XiMat	blood
42	chr3:137780600-137786200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
43	chr3:137780600-137787200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr3:137780600-137787400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr3:137780600-137788000	Strong transcription	Fetal Muscle Leg	muscle
46	chr3:137780600-137791600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr3:137780600-137811600	Weak transcription	Psoas Muscle	Psoas
48	chr3:137780800-137784200	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr3:137780800-137800600	Weak transcription	Brain Hippocampus Middle	brain
50	chr3:137781000-137784400	Strong transcription	Cortex derived primary cultured neurospheres	brain

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