Variant report

Variant	nsv875476
Chromosome Location	chr2:181767757-181854997
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1256)
CpG islands
(count:855)
Chromatin interactive
region (count:55)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1256 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:181844944-181845261	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:181848309-181848889	K562	blood:	n/a	n/a
3	ARID3A	chr2:181846011-181846206	K562	blood:	n/a	n/a
4	ARID3A	chr2:181830167-181830210	K562	blood:	n/a	n/a
5	ARID3A	chr2:181848229-181848889	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:181847132-181847681	K562	blood:	n/a	n/a
7	ARID3A	chr2:181819699-181819727	K562	blood:	n/a	n/a
8	ATF1	chr2:181848534-181848827	K562	blood:	n/a	n/a
9	BACH1	chr2:181844981-181845533	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr2:181845802-181846240	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr2:181845947-181846256	K562	blood:	n/a	n/a
12	BACH1	chr2:181847412-181847569	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr2:181802290-181802517	GM12878	blood:	n/a	n/a
14	BATF	chr2:181816745-181817055	GM12878	blood:	n/a	n/a
15	BATF	chr2:181816749-181817049	GM12878	blood:	n/a	n/a
16	BATF	chr2:181802175-181802514	GM12878	blood:	n/a	n/a
17	BATF	chr2:181803180-181803479	GM12878	blood:	n/a	n/a
18	BATF	chr2:181803193-181803490	GM12878	blood:	n/a	n/a
19	BCL3	chr2:181844883-181845249	GM12878	blood:	n/a	chr2:181845036-181845049
20	BCL3	chr2:181844341-181844645	GM12878	blood:	n/a	n/a
21	BCLAF1	chr2:181845029-181845594	GM12878	blood:	n/a	chr2:181845374-181845383 chr2:181845370-181845383 chr2:181845371-181845380 chr2:181845036-181845049 chr2:181845366-181845379 chr2:181845369-181845382 chr2:181845373-181845386
22	BCLAF1	chr2:181845784-181846336	GM12878	blood:	n/a	chr2:181845931-181845944 chr2:181845930-181845943 chr2:181845928-181845941 chr2:181845930-181845939
23	BCLAF1	chr2:181845290-181845625	GM12878	blood:	n/a	chr2:181845374-181845383 chr2:181845370-181845383 chr2:181845371-181845380 chr2:181845366-181845379 chr2:181845369-181845382 chr2:181845373-181845386
24	BHLHE40	chr2:181846032-181846650	K562	blood:	n/a	n/a
25	BHLHE40	chr2:181844636-181845607	HepG2	liver:	n/a	chr2:181845110-181845126 chr2:181845367-181845383
26	BHLHE40	chr2:181844934-181845621	GM12878	blood:	n/a	chr2:181845110-181845126 chr2:181845367-181845383
27	BHLHE40	chr2:181844561-181845571	K562	blood:	n/a	chr2:181845110-181845126 chr2:181845367-181845383
28	BHLHE40	chr2:181834767-181835135	HepG2	liver:	n/a	n/a
29	BHLHE40	chr2:181813225-181813229	K562	blood:	n/a	n/a
30	BRCA1	chr2:181844924-181845152	HepG2	liver:	n/a	n/a
31	BRCA1	chr2:181802286-181802453	GM12878	blood:	n/a	n/a
32	BRCA1	chr2:181846012-181846207	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr2:181845331-181845539	H1-hESC	embryonic stem cell:	n/a	n/a
34	CBX3	chr2:181844245-181845648	K562	blood:	n/a	n/a
35	CCNT2	chr2:181830250-181830623	K562	blood:	n/a	n/a
36	CCNT2	chr2:181844593-181846420	K562	blood:	n/a	n/a
37	CCNT2	chr2:181844153-181844351	K562	blood:	n/a	n/a
38	CEBPB	chr2:181769816-181770108	HepG2	liver:	n/a	chr2:181769946-181769957 chr2:181769977-181769994
39	CEBPB	chr2:181803175-181803475	IMR90	lung:	n/a	chr2:181803217-181803228
40	CEBPB	chr2:181769828-181770107	A549	lung:	n/a	chr2:181769946-181769957 chr2:181769977-181769994
41	CEBPB	chr2:181834828-181835101	MCF-7	breast:	n/a	n/a
42	CEBPB	chr2:181768011-181768188	A549	lung:	n/a	n/a
43	CEBPB	chr2:181803258-181803436	HepG2	liver:	n/a	n/a
44	CEBPB	chr2:181840322-181840637	HepG2	liver:	n/a	chr2:181840495-181840508 chr2:181840495-181840508 chr2:181840495-181840506 chr2:181840497-181840508 chr2:181840495-181840508
45	CEBPB	chr2:181849868-181850119	IMR90	lung:	n/a	n/a
46	CEBPB	chr2:181840336-181840643	IMR90	lung:	n/a	chr2:181840495-181840508 chr2:181840495-181840508 chr2:181840495-181840506 chr2:181840497-181840508 chr2:181840495-181840508
47	CEBPB	chr2:181806279-181806566	HepG2	liver:	n/a	chr2:181806429-181806440
48	CEBPB	chr2:181769808-181770104	IMR90	lung:	n/a	chr2:181769946-181769957 chr2:181769977-181769994
49	CEBPB	chr2:181769776-181770179	H1-hESC	embryonic stem cell:	n/a	chr2:181769946-181769957 chr2:181769977-181769994
50	CEBPB	chr2:181845348-181845474	H1-hESC	embryonic stem cell:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:181843895-181843945	GM12892	blood:	n/a
2	chr2:181843895-181843945	GM12892	blood:	n/a
3	chr2:181842270-181842320	NHBE	bronchial:	n/a
4	chr2:181846182-181846232	HepG2	liver:	n/a
5	chr2:181843717-181843767	GM06990	blood:	n/a
6	chr2:181843895-181843945	HNPCEpiC	eye:	n/a
7	chr2:181843895-181843945	MCF10A-Er-Src	breast:	n/a
8	chr2:181845502-181845552	HUVEC	blood vessel:	n/a
9	chr2:181845411-181845461	GM06990	blood:	n/a
10	chr2:181845489-181845539	HCM	heart:	n/a
11	chr2:181843717-181843767	SK-N-MC	brain:	n/a
12	chr2:181845502-181845552	NHBE	bronchial:	n/a
13	chr2:181845005-181845055	ProgFib	skin:	n/a
14	chr2:181843895-181843945	GM06990	blood:	n/a
15	chr2:181843717-181843767	SKMC	muscle:	n/a
16	chr2:181851803-181851853	HAEpiC	amniotic membrane:	n/a
17	chr2:181845489-181845539	HRCEpiC	kidney:	n/a
18	chr2:181845502-181845552	HEEpiC	esophagus:	n/a
19	chr2:181844876-181844926	HIPEpiC	eye:	n/a
20	chr2:181849325-181849375	GM12892	blood:	n/a
21	chr2:181851803-181851853	MCF-7	breast:	n/a
22	chr2:181845005-181845055	HIPEpiC	eye:	n/a
23	chr2:181845005-181845055	ovcar-3	ovarian:	n/a
24	chr2:181851803-181851853	BJ	skin:	n/a
25	chr2:181769759-181769809	GM12878	blood:	n/a
26	chr2:181845005-181845055	Caco-2	colon:	n/a
27	chr2:181845502-181845552	HEK293	kidney:	embryo
28	chr2:181845489-181845539	GM12878	blood:	n/a
29	chr2:181851803-181851853	HUVEC	blood vessel:	n/a
30	chr2:181843895-181843945	HEK293	kidney:	embryo
31	chr2:181845005-181845055	Jurkat	blood:	n/a
32	chr2:181845502-181845552	GM12878	blood:	n/a
33	chr2:181845489-181845539	A549	lung:	n/a
34	chr2:181843717-181843767	K562	blood:	n/a
35	chr2:181843717-181843767	AG04449	skin:	fetal
36	chr2:181843183-181843233	SK-N-SH	brain:	n/a
37	chr2:181845489-181845539	SAEC	small airway:	n/a
38	chr2:181845502-181845552	A549	lung:	n/a
39	chr2:181844876-181844926	HEEpiC	esophagus:	n/a
40	chr2:181843183-181843233	BJ	skin:	n/a
41	chr2:181843895-181843945	HRCEpiC	kidney:	n/a
42	chr2:181842270-181842320	PFSK-1	brain:	n/a
43	chr2:181842270-181842320	H1-hESC	embryonic stem cell:	embryo
44	chr2:181845489-181845539	ProgFib	skin:	n/a
45	chr2:181845411-181845461	HUVEC	blood vessel:	n/a
46	chr2:181849325-181849375	HIPEpiC	eye:	n/a
47	chr2:181843895-181843945	HepG2	liver:	n/a
48	chr2:181843183-181843233	HCF	heart:	n/a
49	chr2:181846182-181846232	NHDF-neo	bronchial:	n/a
50	chr2:181851803-181851853	Caco-2	colon:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:181826108..181828377-chr2:181844681..181846891,2	MCF-7	breast:
2	chr2:181767652..181770556-chr2:181770717..181772218,2	MCF-7	breast:
3	chr2:181839506..181842433-chr2:181971642..181974430,2	K562	blood:
4	chr2:181829627..181832228-chr2:181834679..181836392,2	K562	blood:
5	chr2:181810421..181812271-chr2:181830979..181832547,2	K562	blood:
6	chr2:181850460..181852224-chr2:181912252..181913801,2	K562	blood:
7	chr2:181837058..181842990-chr2:181843184..181846817,5	MCF-7	breast:
8	chr2:181790014..181791794-chr2:181795604..181797890,2	K562	blood:
9	chr2:181837425..181840386-chr2:181840573..181842119,2	MCF-7	breast:
10	chr2:181849955..181852390-chr2:181948702..181951416,2	K562	blood:
11	chr2:181841919..181843877-chr9:92475300..92478047,2	MCF-7	breast:
12	chr2:181823528..181825783-chr2:181849129..181851147,2	K562	blood:
13	chr2:181839700..181842326-chr2:181868169..181869713,2	K562	blood:
14	chr2:181770939..181772876-chr2:181773303..181775237,2	K562	blood:
15	chr2:181821769..181824895-chr2:181843465..181846009,3	K562	blood:
16	chr2:181808930..181811570-chr2:181816470..181818302,2	K562	blood:
17	chr2:181808813..181811337-chr2:181812408..181815034,2	K562	blood:
18	chr2:181854710..181856581-chr2:181858874..181861007,2	MCF-7	breast:
19	chr2:181796970..181799324-chr2:181800008..181802884,3	K562	blood:
20	chr2:181814712..181816539-chr2:181818090..181819594,2	K562	blood:
21	chr2:181826791..181830304-chr2:181843129..181846500,4	K562	blood:
22	chr2:181825164..181827909-chr2:181831566..181833281,2	K562	blood:
23	chr2:181782531..181784428-chr2:181828590..181830396,2	K562	blood:
24	chr2:181814712..181816539-chr2:181818090..181819594,2	K562	blood:
25	chr2:181796832..181799715-chr2:181825306..181827387,2	MCF-7	breast:
26	chr2:181799357..181801907-chr2:181843560..181846507,2	K562	blood:
27	chr2:181834069..181839836-chr2:181842561..181845920,7	MCF-7	breast:
28	chr2:181829069..181832020-chr2:181844085..181846532,2	MCF-7	breast:
29	chr2:181845181..181847277-chr7:100464247..100466142,2	MCF-7	breast:
30	chr2:181829069..181832020-chr2:181844085..181846532,2	MCF-7	breast:
31	chr2:181796832..181799715-chr2:181825306..181827387,2	MCF-7	breast:
32	chr2:181767652..181770556-chr2:181770717..181772218,2	MCF-7	breast:
33	chr2:181765622..181768152-chr2:181788241..181790151,2	K562	blood:
34	chr2:181826154..181829123-chr2:181833838..181836698,3	K562	blood:
35	chr2:181770939..181772876-chr2:181773303..181775237,2	K562	blood:
36	chr2:181808930..181811570-chr2:181816470..181818302,2	K562	blood:
37	chr2:181773855..181776189-chr2:181844556..181847410,2	MCF-7	breast:
38	chr2:181823528..181825783-chr2:181849129..181851147,2	K562	blood:
39	chr2:181762102..181764574-chr2:181766840..181768523,2	MCF-7	breast:
40	chr2:181829308..181831127-chr2:181833538..181836179,2	K562	blood:
41	chr2:181555811..181558550-chr2:181846192..181848337,2	K562	blood:
42	chr2:181829308..181831127-chr2:181833538..181836179,2	K562	blood:
43	chr2:181816772..181818990-chr2:181821114..181822961,2	K562	blood:
44	chr2:181796970..181799324-chr2:181800008..181802884,3	K562	blood:
45	chr2:181845093..181847328-chr2:182755996..182757943,2	K562	blood:
46	chr2:181765622..181768152-chr2:181788241..181790151,2	K562	blood:
47	chr2:181843873..181847676-chr2:181852580..181857298,4	MCF-7	breast:
48	chr2:181826154..181829123-chr2:181833838..181836698,3	K562	blood:
49	chr2:181816772..181818990-chr2:181821114..181822961,2	K562	blood:
50	chr2:181837425..181840386-chr2:181840573..181842119,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UBE2E3-2	chr2:181781000-181781666	NR_104325
2	lnc-UBE2E3-2	chr2:181781000-181781666	NR_104319
3	lnc-UBE2E3-2	chr2:181781000-181781666	NR_104321
4	lnc-UBE2E3-2	chr2:181771313-181774666	NONHSAT075852
5	lnc-UBE2E3-2	chr2:181779561-181785974	NONHSAT075852
6	lnc-CERKL-3	chr2:181844154-181844393	ENSG00000236153.1
7	lnc-UBE2E3-4	chr2:181799443-181799507	ucscGeneNc_uc002uns_1
8	lnc-UBE2E3-2	chr2:181781000-181781666	NR_104320
9	lnc-UBE2E3-2	chr2:181781000-181781666	NR_104324
10	lnc-UBE2E3-2	chr2:181781000-181781666	NR_104323
11	lnc-CERKL-3	chr2:181844793-181844817	ENSG00000236153.1
12	lnc-UBE2E3-2	chr2:181781000-181781666	NR_104322
13	lnc-UBE2E3-4	chr2:181835801-181835949	ucscGeneNc_uc002uns_1

No data

Variant related genes	Relation type
UBE2E3	TF binding region
ENSG00000236153	TF binding region
ENSG00000236667	TF binding region
UBE2E3	CpG island
ENSG00000236153	CpG island
ENSG00000236667	CpG island
ENSG00000087077	chromatin interactions
ENSG00000170035	chromatin interactions
ENSG00000225258	chromatin interactions
ENSG00000260742	chromatin interactions
ENSG00000236153	chromatin interactions
ENSG00000138434	chromatin interactions

Extended variants
information (count: 2336 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:2336 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10178400	chr2:181767757-181767758	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs190889463	chr2:181767765-181767766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572907428	chr2:181767854-181767855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142626040	chr2:181767861-181767862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs182833876	chr2:181767913-181767914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs555650387	chr2:181767938-181767939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150582004	chr2:181767955-181767956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549189802	chr2:181767956-181767957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs377386040	chr2:181767991-181767992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs368834485	chr2:181768032-181768033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs544077595	chr2:181768042-181768043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561205310	chr2:181768080-181768081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188934272	chr2:181768115-181768116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs193260518	chr2:181768269-181768270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs139622626	chr2:181768270-181768271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs78237107	chr2:181768282-181768283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs551450874	chr2:181768291-181768292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565238862	chr2:181768332-181768333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs183208064	chr2:181768368-181768369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550910277	chr2:181768431-181768432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552459000	chr2:181768447-181768448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs201266336	chr2:181768559-181768560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs373343035	chr2:181768560-181768561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536525807	chr2:181768564-181768565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571568781	chr2:181768658-181768659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563387760	chr2:181768679-181768680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs547366174	chr2:181768723-181768724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs566469026	chr2:181768728-181768729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533806283	chr2:181768773-181768774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs67278994	chr2:181768791-181768792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538650947	chr2:181768798-181768799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs558636339	chr2:181768800-181768801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs35101921	chr2:181768801-181768802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs563041114	chr2:181768802-181768803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs201724409	chr2:181768804-181768805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs554449397	chr2:181768817-181768818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs7609144	chr2:181768863-181768864	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs74744913	chr2:181768866-181768867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs536380159	chr2:181768899-181768900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149760594	chr2:181768924-181768925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs545023003	chr2:181768933-181768934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs570638293	chr2:181768971-181768972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530894749	chr2:181769008-181769009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187587574	chr2:181769071-181769072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs561322394	chr2:181769112-181769113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs530362041	chr2:181769119-181769120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547277300	chr2:181769181-181769182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs192010310	chr2:181769188-181769189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs532114460	chr2:181769221-181769222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs117257578	chr2:181769223-181769224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:49)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Sudden cardiac death	19188705	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	21062444	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:1155 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:181763600-181769400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr2:181767600-181767800	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr2:181767600-181771000	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr2:181767800-181768000	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr2:181767800-181768000	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr2:181767800-181768000	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr2:181768200-181769400	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr2:181768200-181769400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr2:181768400-181768600	Enhancers	Fetal Lung	lung
10	chr2:181768800-181769400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr2:181768800-181770000	Weak transcription	Fetal Lung	lung
12	chr2:181769200-181770800	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr2:181769400-181769600	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr2:181769400-181769600	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr2:181769400-181769600	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr2:181769400-181770800	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr2:181769600-181769800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr2:181769600-181769800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
19	chr2:181769600-181770000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
20	chr2:181769600-181770000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr2:181769600-181770600	Enhancers	HSMM	muscle
22	chr2:181769600-181770800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr2:181769800-181770000	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr2:181769800-181770000	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr2:181769800-181770000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr2:181769800-181770800	Enhancers	H1 Cell Line	embryonic stem cell
27	chr2:181769800-181770800	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr2:181770000-181770200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr2:181770000-181770200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
30	chr2:181770000-181770400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
31	chr2:181770000-181770800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr2:181770000-181771000	Enhancers	Fetal Lung	lung
33	chr2:181770000-181772000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr2:181770200-181770600	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr2:181770200-181770800	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr2:181770400-181770600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr2:181770400-181770600	Enhancers	Muscle Satellite Cultured Cells	--
38	chr2:181770400-181770800	Enhancers	Fetal Heart	heart
39	chr2:181770600-181770800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr2:181770600-181772400	Weak transcription	HSMM	muscle
41	chr2:181770800-181771600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr2:181770800-181771800	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr2:181770800-181772200	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr2:181770800-181772400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr2:181770800-181775400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr2:181771000-181771400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr2:181771000-181772000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr2:181771000-181772600	Weak transcription	Fetal Lung	lung
49	chr2:181771400-181771800	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr2:181771600-181772000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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