Variant report

Variant	nsv873808
Chromosome Location	chr2:34275757-34703057
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	chr2:34492233-34492695	GM12878	blood:	n/a	n/a
2	ATF2	chr2:34590863-34591498	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:34321987-34322130	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr2:34516235-34516448	GM12878	blood:	n/a	n/a
5	BATF	chr2:34626271-34626588	GM12878	blood:	n/a	chr2:34626402-34626412 chr2:34626401-34626412
6	BATF	chr2:34516238-34516504	GM12878	blood:	n/a	n/a
7	BATF	chr2:34492248-34492667	GM12878	blood:	n/a	chr2:34492484-34492495
8	BATF	chr2:34626250-34626627	GM12878	blood:	n/a	chr2:34626402-34626412 chr2:34626401-34626412
9	BATF	chr2:34492306-34492669	GM12878	blood:	n/a	chr2:34492484-34492495
10	BCL11A	chr2:34492295-34492624	GM12878	blood:	n/a	n/a
11	BCL11A	chr2:34591088-34591422	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr2:34626351-34626529	GM12878	blood:	n/a	chr2:34626400-34626409 chr2:34626401-34626410
13	BCL3	chr2:34633202-34633571	GM12878	blood:	n/a	chr2:34633318-34633327 chr2:34633317-34633326
14	BCL3	chr2:34633212-34633509	GM12878	blood:	n/a	chr2:34633318-34633327 chr2:34633317-34633326
15	BHLHE40	chr2:34492074-34492695	GM12878	blood:	n/a	n/a
16	BHLHE40	chr2:34318851-34319200	GM12878	blood:	n/a	n/a
17	BHLHE40	chr2:34633159-34633448	GM12878	blood:	n/a	n/a
18	BRCA1	chr2:34321723-34321955	H1-hESC	embryonic stem cell:	n/a	n/a
19	CBX3	chr2:34435457-34435788	K562	blood:	n/a	n/a
20	CBX3	chr2:34435491-34435729	K562	blood:	n/a	n/a
21	CCNT2	chr2:34623370-34623530	K562	blood:	n/a	n/a
22	CEBPB	chr2:34637703-34637950	MCF-7	breast:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
23	CEBPB	chr2:34661633-34661923	HepG2	liver:	n/a	chr2:34661857-34661869
24	CEBPB	chr2:34610798-34611191	HepG2	liver:	n/a	chr2:34610999-34611008 chr2:34611030-34611038 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610999-34611008 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610997-34611008 chr2:34610997-34611010 chr2:34610998-34611009 chr2:34610997-34611008
25	CEBPB	chr2:34414995-34415284	K562	blood:	n/a	chr2:34415149-34415160
26	CEBPB	chr2:34651788-34652080	HepG2	liver:	n/a	chr2:34651953-34651964
27	CEBPB	chr2:34415007-34415328	A549	lung:	n/a	chr2:34415149-34415160
28	CEBPB	chr2:34327416-34327754	IMR90	lung:	n/a	n/a
29	CEBPB	chr2:34315236-34315504	HepG2	liver:	n/a	chr2:34315355-34315366
30	CEBPB	chr2:34390889-34391003	K562	blood:	n/a	n/a
31	CEBPB	chr2:34435519-34435730	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr2:34651815-34652025	H1-hESC	embryonic stem cell:	n/a	chr2:34651953-34651964
33	CEBPB	chr2:34440267-34440614	A549	lung:	n/a	chr2:34440437-34440448
34	CEBPB	chr2:34431949-34432159	HepG2	liver:	n/a	chr2:34432104-34432115
35	CEBPB	chr2:34575982-34576211	HepG2	liver:	n/a	chr2:34576118-34576129
36	CEBPB	chr2:34331718-34332056	HepG2	liver:	n/a	chr2:34331898-34331909
37	CEBPB	chr2:34415049-34415217	H1-hESC	embryonic stem cell:	n/a	chr2:34415149-34415160
38	CEBPB	chr2:34610823-34611180	IMR90	lung:	n/a	chr2:34610999-34611008 chr2:34611030-34611038 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610999-34611008 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610997-34611008 chr2:34610997-34611010 chr2:34610998-34611009 chr2:34610997-34611008
39	CEBPB	chr2:34440301-34440596	K562	blood:	n/a	chr2:34440437-34440448
40	CEBPB	chr2:34610850-34611138	MCF-7	breast:	n/a	chr2:34610999-34611008 chr2:34611030-34611038 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610999-34611008 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610997-34611008 chr2:34610997-34611010 chr2:34610998-34611009 chr2:34610997-34611008
41	CEBPB	chr2:34512235-34512435	HepG2	liver:	n/a	chr2:34512358-34512369 chr2:34512358-34512371
42	CEBPB	chr2:34422914-34423093	HepG2	liver:	n/a	chr2:34422978-34422987 chr2:34422978-34422987 chr2:34422976-34422987
43	CEBPB	chr2:34634613-34634777	A549	lung:	n/a	n/a
44	CEBPB	chr2:34331757-34332067	IMR90	lung:	n/a	chr2:34331898-34331909
45	CEBPB	chr2:34331823-34332032	H1-hESC	embryonic stem cell:	n/a	chr2:34331898-34331909
46	CEBPB	chr2:34440259-34440615	IMR90	lung:	n/a	chr2:34440437-34440448
47	CEBPB	chr2:34384835-34384887	K562	blood:	n/a	chr2:34384844-34384855
48	CEBPB	chr2:34637613-34637978	K562	blood:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
49	CEBPB	chr2:34637693-34638019	A549	lung:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
50	CEBPB	chr2:34633778-34633979	HepG2	liver:	n/a	chr2:34633880-34633891 chr2:34633878-34633891 chr2:34633878-34633889 chr2:34633878-34633891

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:34590591-34590641	NHDF-neo	bronchial:	n/a
2	chr2:34633637-34633687	PrEC	prostate:	n/a
3	chr2:34590591-34590641	AG04450	lung:	fetal
4	chr2:34633637-34633687	ProgFib	skin:	n/a
5	chr2:34590591-34590641	NH-A	brain:	n/a
6	chr2:34633637-34633687	SAEC	small airway:	n/a
7	chr2:34633637-34633687	AG10803	skin:	n/a
8	chr2:34590591-34590641	AG10803	skin:	n/a
9	chr2:34590591-34590641	ECC-1	luminal epithelium:	n/a
10	chr2:34590591-34590641	BE2_C	brain:	n/a
11	chr2:34633637-34633687	PANC-1	pancreas:	n/a
12	chr2:34590591-34590641	ProgFib	skin:	n/a
13	chr2:34590591-34590641	HCPEpiC	choroid plexus:	n/a
14	chr2:34633637-34633687	Jurkat	blood:	n/a
15	chr2:34590591-34590641	HCT-116	colon:	n/a
16	chr2:34590591-34590641	HEK293	kidney:	embryo
17	chr2:34590591-34590641	IMR90	lung:	fetal
18	chr2:34633637-34633687	MCF10A-Er-Src	breast:	n/a
19	chr2:34633637-34633687	GM12891	blood:	n/a
20	chr2:34590591-34590641	AG04449	skin:	fetal
21	chr2:34590591-34590641	HRPEpiC	eye:	n/a
22	chr2:34590591-34590641	AG09319	gingival:	n/a
23	chr2:34633637-34633687	HCT-116	colon:	n/a
24	chr2:34633637-34633687	Caco-2	colon:	n/a
25	chr2:34633637-34633687	AG09319	gingival:	n/a
26	chr2:34590591-34590641	PrEC	prostate:	n/a
27	chr2:34590591-34590641	NHBE	bronchial:	n/a
28	chr2:34590591-34590641	HRCEpiC	kidney:	n/a
29	chr2:34590591-34590641	AG09309	skin:	n/a
30	chr2:34590591-34590641	HUVEC	blood vessel:	n/a
31	chr2:34590591-34590641	Hepatocyte	liver:	n/a
32	chr2:34633637-34633687	HEEpiC	esophagus:	n/a
33	chr2:34633637-34633687	A549	lung:	n/a
34	chr2:34633637-34633687	HMEC	breast:	n/a
35	chr2:34590591-34590641	H1-hESC	embryonic stem cell:	embryo
36	chr2:34590591-34590641	T-47D	breast:	n/a
37	chr2:34633637-34633687	Hela-S3	cervix:	n/a
38	chr2:34633637-34633687	HCF	heart:	n/a
39	chr2:34633637-34633687	HIPEpiC	eye:	n/a
40	chr2:34633637-34633687	NB4	blood:	n/a
41	chr2:34633637-34633687	H1-hESC	embryonic stem cell:	embryo
42	chr2:34633637-34633687	HNPCEpiC	eye:	n/a
43	chr2:34590591-34590641	NT2-D1	testis:	n/a
44	chr2:34633637-34633687	GM12878	blood:	n/a
45	chr2:34590591-34590641	HAEpiC	amniotic membrane:	n/a
46	chr2:34590591-34590641	GM12891	blood:	n/a
47	chr2:34633637-34633687	SKMC	muscle:	n/a
48	chr2:34633637-34633687	NHDF-neo	bronchial:	n/a
49	chr2:34633637-34633687	MCF-7	breast:	n/a
50	chr2:34633637-34633687	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:34237451..34238372-chr2:34321266..34322187,3	MCF-7	breast:
2	chr2:34636657..34638446-chr2:34644514..34646250,2	K562	blood:
3	chr2:34590795..34592507-chr2:34600278..34603033,2	K562	blood:
4	chr2:34321239..34322372-chr2:34772370..34773083,4	MCF-7	breast:
5	chr2:34520994..34523413-chr2:34524356..34526580,2	MCF-7	breast:
6	chr2:34624209..34626557-chr2:34688886..34690644,2	K562	blood:
7	chr2:33906087..33906631-chr2:34321375..34322022,2	MCF-7	breast:
8	chr2:34541264..34543781-chr2:34553502..34555371,2	MCF-7	breast:
9	chr2:34334993..34337694-chr2:34340157..34342643,2	K562	blood:
10	chr2:34324491..34327338-chr2:34327561..34329321,2	MCF-7	breast:
11	chr2:34321381..34322557-chr2:34795669..34796275,5	MCF-7	breast:
12	chr2:34401156..34402823-chr2:34426410..34428532,2	K562	blood:
13	chr2:34469910..34471896-chr2:34475795..34477495,2	MCF-7	breast:
14	chr2:34541264..34543781-chr2:34553502..34555371,2	MCF-7	breast:
15	chr12:46765173..46767943-chr2:34590937..34593382,2	MCF-7	breast:
16	chr2:34451708..34454413-chr2:34493747..34495311,2	K562	blood:
17	chr2:34624209..34626557-chr2:34688886..34690644,2	K562	blood:
18	chr2:34401156..34402823-chr2:34426410..34428532,2	K562	blood:
19	chr2:34590795..34592507-chr2:34600278..34603033,2	K562	blood:
20	chr2:34469910..34471896-chr2:34475795..34477495,2	MCF-7	breast:
21	chr17:57969237..57970939-chr2:34675539..34678526,2	MCF-7	breast:
22	chr2:34324491..34327338-chr2:34327561..34329321,2	MCF-7	breast:
23	chr2:34334993..34337694-chr2:34340157..34342643,2	K562	blood:
24	chr2:34636657..34638446-chr2:34644514..34646250,2	K562	blood:
25	chr17:41466170..41467868-chr2:34623111..34624611,2	MCF-7	breast:
26	chr2:34416041..34418842-chr2:34421357..34424092,2	K562	blood:
27	chr2:34520994..34523413-chr2:34524356..34526580,2	MCF-7	breast:
28	chr2:34416041..34418842-chr2:34421357..34424092,2	K562	blood:
29	chr2:34437642..34440323-chr2:34446994..34448643,2	K562	blood:
30	chr2:34437642..34440323-chr2:34446994..34448643,2	K562	blood:
31	chr2:34451708..34454413-chr2:34493747..34495311,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASGRP3-3	chr2:34609584-34609636	ENSG00000226785
2	lnc-RASGRP3-2	chr2:34293281-34293347	XLOC_001422
3	lnc-RASGRP3-13	chr2:34462359-34462780	NONHSAT070033
4	lnc-RASGRP3-3	chr2:34609584-34609796	NONHSAT070034
5	lnc-RASGRP3-2	chr2:34284362-34284586	NONHSAT070031
6	lnc-RASGRP3-13	chr2:34463088-34463140	NONHSAT070033
7	lnc-RASGRP3-2	chr2:34288818-34293939	NONHSAT070031
8	lnc-RASGRP3-1	chr2:34511710-34511813	ENSG00000203386
9	lnc-RASGRP3-1	chr2:34522535-34522820	ENSG00000203386
10	lnc-RASGRP3-3	chr2:34511701-34511813	NONHSAT070034
11	lnc-RASGRP3-3	chr2:34608855-34609276	ENSG00000226785
12	lnc-RASGRP3-2	chr2:34292293-34292370	XLOC_001422
13	lnc-RASGRP3-1	chr2:34285817-34285994	ENSG00000203386
14	lnc-RASGRP3-2	chr2:34294166-34294617	XLOC_001422
15	lnc-RASGRP3-1	chr2:34286086-34286114	ENSG00000203386

Variant related genes	Relation type
ENSG00000212025	TF binding region
ENSG00000226785	TF binding region
ENSG00000237790	TF binding region
ENSG00000212025	CpG island
ENSG00000226785	CpG island
ENSG00000237790	CpG island
ENSG00000108423	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000134294	chromatin interactions
ENSG00000108443	chromatin interactions
ENSG00000258096	chromatin interactions

Extended variants
information (count: 7667 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:7667 , 50 per page) page: 1 2 3 4 5 6 7 ... 154

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4670315	chr2:34275757-34275758	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs75762229	chr2:34275772-34275773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs539370765	chr2:34275794-34275795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs146381110	chr2:34275835-34275836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs6744782	chr2:34275884-34275885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535630957	chr2:34275887-34275888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs377216175	chr2:34275932-34275933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs375992072	chr2:34275946-34275947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs200925073	chr2:34275947-34275948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs554415592	chr2:34275948-34275949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs554810668	chr2:34275954-34275955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs397810114	chr2:34275955-34275956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs6716688	chr2:34275956-34275957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370273977	chr2:34275963-34275964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs139096972	chr2:34275967-34275968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs374345998	chr2:34275972-34275973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs2887158	chr2:34275974-34275975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs370061637	chr2:34275985-34275986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs569593450	chr2:34284364-34284365	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs538628972	chr2:34284405-34284406	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs58080018	chr2:34284412-34284413	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs371096135	chr2:34284414-34284415	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs552218480	chr2:34284418-34284419	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs565947105	chr2:34284496-34284497	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs10192086	chr2:34284574-34284575	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs574244717	chr2:34284630-34284631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs536354893	chr2:34284638-34284639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs556609420	chr2:34284642-34284643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs528819821	chr2:34284666-34284667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142254295	chr2:34284680-34284681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11302436	chr2:34284748-34284749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs34057795	chr2:34284759-34284760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs540263169	chr2:34284764-34284765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs558646091	chr2:34284788-34284789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs562149568	chr2:34284802-34284803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs181225547	chr2:34284820-34284821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs561477371	chr2:34284835-34284836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs368128813	chr2:34284842-34284843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs9308945	chr2:34284852-34284853	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
40	rs10179886	chr2:34284855-34284856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532047909	chr2:34284861-34284862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs552163859	chr2:34284920-34284921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs187096760	chr2:34284939-34284940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528371388	chr2:34284948-34284949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs57496052	chr2:34284961-34284962	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs569014917	chr2:34284970-34284971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs6711736	chr2:34284984-34284985	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
48	rs146826653	chr2:34285009-34285010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs556409599	chr2:34285036-34285037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs530477548	chr2:34285059-34285060	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
Autism	22495309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Glioma	20126413	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Incontinentia Pigmenti	22033527	CNVD
Alcoholism	22295116	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:464 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:34275000-34276000	Enhancers	Fetal Heart	heart
2	chr2:34284600-34285200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr2:34293000-34293200	Enhancers	Brain Hippocampus Middle	brain
4	chr2:34293000-34293600	Enhancers	Brain Substantia Nigra	brain
5	chr2:34293400-34294800	Weak transcription	Brain Hippocampus Middle	brain
6	chr2:34293600-34295000	Weak transcription	Brain Substantia Nigra	brain
7	chr2:34294200-34294600	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr2:34294200-34295200	Enhancers	Brain Cingulate Gyrus	brain
9	chr2:34294200-34295800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr2:34294400-34294800	Enhancers	Brain Anterior Caudate	brain
11	chr2:34294600-34296200	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr2:34294800-34295000	Enhancers	Brain Hippocampus Middle	brain
13	chr2:34295000-34295400	Flanking Active TSS	Brain Hippocampus Middle	brain
14	chr2:34295000-34295400	Enhancers	Brain Substantia Nigra	brain
15	chr2:34295200-34295400	Flanking Active TSS	Brain Cingulate Gyrus	brain
16	chr2:34295400-34296200	Weak transcription	Brain Substantia Nigra	brain
17	chr2:34295400-34296400	Active TSS	Brain Cingulate Gyrus	brain
18	chr2:34295400-34296400	Enhancers	Brain Hippocampus Middle	brain
19	chr2:34296200-34296600	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr2:34296200-34296600	ZNF genes & repeats	Brain Substantia Nigra	brain
21	chr2:34305800-34306400	Enhancers	Fetal Intestine Large	intestine
22	chr2:34320600-34320800	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr2:34320800-34321800	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr2:34320800-34322400	Enhancers	Brain Hippocampus Middle	brain
25	chr2:34321400-34322200	Enhancers	Brain Angular Gyrus	brain
26	chr2:34321400-34322200	Enhancers	Brain Substantia Nigra	brain
27	chr2:34321800-34322200	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr2:34322800-34323600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr2:34324400-34326600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr2:34324800-34325000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr2:34325200-34329600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr2:34325600-34326000	Enhancers	Colon Smooth Muscle	Colon
33	chr2:34325600-34326000	Enhancers	HUVEC	blood vessel
34	chr2:34325600-34326200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr2:34326000-34327400	Weak transcription	HUVEC	blood vessel
36	chr2:34326200-34329200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr2:34327000-34329600	Enhancers	NHEK	skin
38	chr2:34327200-34328400	Enhancers	HMEC	breast
39	chr2:34327400-34329600	Enhancers	HUVEC	blood vessel
40	chr2:34327600-34327800	Enhancers	NH-A	brain
41	chr2:34327800-34328000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr2:34327800-34328000	Enhancers	Osteobl	bone
43	chr2:34328000-34329000	Weak transcription	NH-A	brain
44	chr2:34328000-34330000	Enhancers	Muscle Satellite Cultured Cells	--
45	chr2:34328400-34329600	Weak transcription	HMEC	breast
46	chr2:34328400-34330200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr2:34328600-34329600	Weak transcription	Osteobl	bone
48	chr2:34329000-34329600	Enhancers	NH-A	brain
49	chr2:34329200-34329600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr2:34329400-34330200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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