Variant report

Variant	nsv525350
Chromosome Location	chr2:151711700-152044794
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2186)
CpG islands
(count:794)
Chromatin interactive
region (count:72)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2186 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:151908139-151908434	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:151793632-151793868	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:151908178-151908448	K562	blood:	n/a	n/a
4	ATF1	chr2:151908182-151908476	K562	blood:	n/a	n/a
5	ATF1	chr2:151875216-151875322	K562	blood:	n/a	n/a
6	ATF1	chr2:151729141-151729143	K562	blood:	n/a	n/a
7	ATF1	chr2:151734966-151735152	K562	blood:	n/a	n/a
8	ATF2	chr2:151968209-151968790	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr2:151734845-151735112	K562	blood:	n/a	n/a
10	BACH1	chr2:151768470-151768826	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr2:151968125-151968482	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr2:151838479-151838684	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr2:151725646-151725845	H1-hESC	embryonic stem cell:	n/a	n/a
14	BHLHE40	chr2:151908172-151908372	K562	blood:	n/a	n/a
15	BHLHE40	chr2:151768205-151768407	A549	lung:	n/a	n/a
16	BHLHE40	chr2:151768222-151768762	HepG2	liver:	n/a	n/a
17	BHLHE40	chr2:151868020-151868230	K562	blood:	n/a	n/a
18	BHLHE40	chr2:151733399-151733404	K562	blood:	n/a	n/a
19	BRCA1	chr2:151849729-151849808	GM12878	blood:	n/a	n/a
20	CBX3	chr2:151908023-151908538	HCT-116	colon:	n/a	n/a
21	CBX3	chr2:151734760-151735340	HCT-116	colon:	n/a	n/a
22	CBX3	chr2:151968193-151968519	HCT-116	colon:	n/a	n/a
23	CBX3	chr2:151723010-151723332	K562	blood:	n/a	n/a
24	CCNT2	chr2:151943825-151943916	K562	blood:	n/a	n/a
25	CEBPB	chr2:151865587-151865663	Hela-S3	cervix:	n/a	chr2:151865627-151865636 chr2:151865627-151865638 chr2:151865625-151865636
26	CEBPB	chr2:151805207-151805500	HepG2	liver:	n/a	chr2:151805345-151805356
27	CEBPB	chr2:151850580-151850832	IMR90	lung:	n/a	n/a
28	CEBPB	chr2:151741689-151742024	K562	blood:	n/a	chr2:151741859-151741872 chr2:151741860-151741871
29	CEBPB	chr2:151805263-151805445	HepG2	liver:	n/a	chr2:151805345-151805356
30	CEBPB	chr2:151768168-151768881	A549	lung:	n/a	chr2:151768357-151768368 chr2:151768356-151768369 chr2:151768358-151768367 chr2:151768356-151768369 chr2:151768356-151768369 chr2:151768356-151768367 chr2:151768358-151768367 chr2:151768358-151768367 chr2:151768358-151768367
31	CEBPB	chr2:152018665-152019024	IMR90	lung:	n/a	n/a
32	CEBPB	chr2:151768190-151768884	H1-hESC	embryonic stem cell:	n/a	chr2:151768357-151768368 chr2:151768356-151768369 chr2:151768358-151768367 chr2:151768356-151768369 chr2:151768356-151768369 chr2:151768356-151768367 chr2:151768358-151768367 chr2:151768358-151768367 chr2:151768358-151768367
33	CEBPB	chr2:151768246-151768514	MCF-7	breast:	n/a	chr2:151768357-151768368 chr2:151768356-151768369 chr2:151768358-151768367 chr2:151768356-151768369 chr2:151768356-151768369 chr2:151768356-151768367 chr2:151768358-151768367 chr2:151768358-151768367 chr2:151768358-151768367
34	CEBPB	chr2:151761930-151762144	HepG2	liver:	n/a	chr2:151761998-151762009
35	CEBPB	chr2:151768230-151768494	ECC-1	luminal epithelium:	n/a	chr2:151768357-151768368 chr2:151768356-151768369 chr2:151768358-151768367 chr2:151768356-151768369 chr2:151768356-151768369 chr2:151768356-151768367 chr2:151768358-151768367 chr2:151768358-151768367 chr2:151768358-151768367
36	CEBPB	chr2:151768202-151768453	HepG2	liver:	n/a	chr2:151768357-151768368 chr2:151768356-151768369 chr2:151768358-151768367 chr2:151768356-151768369 chr2:151768356-151768369 chr2:151768356-151768367 chr2:151768358-151768367 chr2:151768358-151768367 chr2:151768358-151768367
37	CEBPB	chr2:151898004-151898254	HepG2	liver:	n/a	chr2:151898170-151898181 chr2:151898169-151898180
38	CEBPB	chr2:151922466-151922783	IMR90	lung:	n/a	chr2:151922620-151922629 chr2:151922619-151922630 chr2:151922618-151922629
39	CEBPB	chr2:151856317-151856385	HepG2	liver:	n/a	chr2:151856332-151856343
40	CEBPB	chr2:151906194-151906476	IMR90	lung:	n/a	n/a
41	CEBPB	chr2:152042639-152042984	HepG2	liver:	n/a	n/a
42	CEBPB	chr2:151741692-151742063	IMR90	lung:	n/a	chr2:151741859-151741872 chr2:151741860-151741871
43	CEBPB	chr2:151908084-151908558	IMR90	lung:	n/a	n/a
44	CEBPB	chr2:152012519-152012707	A549	lung:	n/a	chr2:152012591-152012602 chr2:152012560-152012571
45	CEBPB	chr2:151734940-151735195	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr2:151885902-151886012	K562	blood:	n/a	chr2:151885978-151885989
47	CEBPB	chr2:152042648-152042868	K562	blood:	n/a	n/a
48	CEBPB	chr2:151885787-151886411	IMR90	lung:	n/a	chr2:151885978-151885989
49	CEBPB	chr2:151751993-151752319	HepG2	liver:	n/a	chr2:151752157-151752168 chr2:151752154-151752171
50	CEBPB	chr2:151741718-151742038	A549	lung:	n/a	chr2:151741859-151741872 chr2:151741860-151741871

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:152006936-152006986	SK-N-SH	brain:	n/a
2	chr2:152006936-152006986	SK-N-SH	brain:	n/a
3	chr2:151889577-151889627	SKMC	muscle:	n/a
4	chr2:151730811-151730861	LNCaP	prostate:	n/a
5	chr2:152006936-152006986	NH-A	brain:	n/a
6	chr2:152018130-152018180	AG04449	skin:	fetal
7	chr2:152018130-152018180	HCT-116	colon:	n/a
8	chr2:152042657-152042707	HCT-116	colon:	n/a
9	chr2:152018130-152018180	NB4	blood:	n/a
10	chr2:151730811-151730861	HCT-116	colon:	n/a
11	chr2:152042675-152042725	GM12891	blood:	n/a
12	chr2:152006936-152006986	NT2-D1	testis:	n/a
13	chr2:151730811-151730861	HPAEpiC	pulmonary alveolar:	n/a
14	chr2:152006936-152006986	BJ	skin:	n/a
15	chr2:151716903-151716953	HCM	heart:	n/a
16	chr2:151730811-151730861	HepG2	liver:	n/a
17	chr2:152032584-152032634	AG10803	skin:	n/a
18	chr2:152042657-152042707	MCF-7	breast:	n/a
19	chr2:151896813-151896863	IMR90	lung:	fetal
20	chr2:151768348-151768398	NB4	blood:	n/a
21	chr2:152032584-152032634	HAEpiC	amniotic membrane:	n/a
22	chr2:151889577-151889627	HCF	heart:	n/a
23	chr2:151896813-151896863	HEK293	kidney:	embryo
24	chr2:152042675-152042725	SK-N-MC	brain:	n/a
25	chr2:152032584-152032634	MCF10A-Er-Src	breast:	n/a
26	chr2:151788471-151788521	U87	brain:	n/a
27	chr2:151788471-151788521	PANC-1	pancreas:	n/a
28	chr2:151768348-151768398	HMEC	breast:	n/a
29	chr2:152032584-152032634	GM19239	blood:	n/a
30	chr2:152006936-152006986	ovcar-3	ovarian:	n/a
31	chr2:151716903-151716953	H1-hESC	embryonic stem cell:	embryo
32	chr2:152006936-152006986	GM12892	blood:	n/a
33	chr2:152018130-152018180	HepG2	liver:	n/a
34	chr2:151716903-151716953	GM19239	blood:	n/a
35	chr2:151889577-151889627	NT2-D1	testis:	n/a
36	chr2:152042657-152042707	ProgFib	skin:	n/a
37	chr2:151716903-151716953	BE2_C	brain:	n/a
38	chr2:151730502-151730552	IMR90	lung:	fetal
39	chr2:151896813-151896863	HL-60	blood:	n/a
40	chr2:151716903-151716953	HAEpiC	amniotic membrane:	n/a
41	chr2:151896813-151896863	GM12878	blood:	n/a
42	chr2:152042675-152042725	HIPEpiC	eye:	n/a
43	chr2:152042675-152042725	HepG2	liver:	n/a
44	chr2:152018130-152018180	T-47D	breast:	n/a
45	chr2:151896813-151896863	HNPCEpiC	eye:	n/a
46	chr2:151730811-151730861	AG04450	lung:	fetal
47	chr2:151730811-151730861	SAEC	small airway:	n/a
48	chr2:151768348-151768398	HL-60	blood:	n/a
49	chr2:151838548-151838598	ProgFib	skin:	n/a
50	chr2:151730811-151730861	K562	blood:	n/a

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:151943398..151945542-chr2:151945977..151948805,2	K562	blood:
2	chr2:151342714..151344287-chr2:151875925..151878501,2	MCF-7	breast:
3	chr2:151908192..151908752-chr2:151928022..151928556,2	MCF-7	breast:
4	chr2:152023638..152026454-chr2:152144557..152146089,2	K562	blood:
5	chr2:151907813..151910172-chr2:151913284..151915565,3	K562	blood:
6	chr2:151713893..151716276-chr2:151721161..151722735,2	K562	blood:
7	chr2:151466968..151467825-chr2:151907836..151908382,2	MCF-7	breast:
8	chr2:151713893..151716276-chr2:151721161..151722735,2	K562	blood:
9	chr2:152014944..152016964-chr2:152019119..152020652,2	K562	blood:
10	chr2:152036783..152038759-chr2:152047666..152049204,2	K562	blood:
11	chr2:152020947..152023552-chr2:152026485..152029371,2	K562	blood:
12	chr2:152020947..152023552-chr2:152026485..152029371,2	K562	blood:
13	chr2:151768362..151769212-chr2:151907879..151908719,2	MCF-7	breast:
14	chr10:5933821..5935712-chr2:151735859..151737363,2	K562	blood:
15	chr2:152015868..152018283-chr2:152021661..152023265,2	MCF-7	breast:
16	chr2:151726245..151728996-chr2:151735766..151738645,2	K562	blood:
17	chr2:151340528..151343485-chr2:151915081..151917487,2	MCF-7	breast:
18	chr2:151872234..151873840-chr2:151877034..151878622,2	MCF-7	breast:
19	chr2:151895774..151898411-chr2:151900217..151902531,2	K562	blood:
20	chr2:152014944..152016964-chr2:152019119..152020652,2	K562	blood:
21	chr2:151999683..152001762-chr2:152019271..152021804,2	MCF-7	breast:
22	chr2:151999581..152002485-chr2:152004385..152006033,2	K562	blood:
23	chr2:152002753..152005696-chr2:152094536..152097046,2	K562	blood:
24	chr2:151846176..151848351-chr2:151852961..151855153,2	K562	blood:
25	chr2:151911293..151912869-chr2:151915243..151918186,2	K562	blood:
26	chr2:151896316..151898182-chr2:151898669..151901241,2	MCF-7	breast:
27	chr2:151883308..151884879-chr2:151887894..151890607,2	K562	blood:
28	chr2:151907813..151910172-chr2:151913284..151915565,3	K562	blood:
29	chr2:151966049..151968023-chr2:151983084..151984640,2	MCF-7	breast:
30	chr2:151913690..151917592-chr2:151920463..151923013,3	K562	blood:
31	chr2:151872234..151873840-chr2:151877034..151878622,2	MCF-7	breast:
32	chr2:151998007..151999659-chr2:152006655..152009074,2	K562	blood:
33	chr2:151834278..151835808-chr2:151846430..151849245,2	K562	blood:
34	chr2:151884261..151886924-chr2:151887279..151889141,2	MCF-7	breast:
35	chr2:150466974..150467880-chr2:151927754..151928650,2	MCF-7	breast:
36	chr2:151729118..151732985-chr2:151733017..151737026,4	K562	blood:
37	chr2:151983352..151983852-chr3:113433304..113434297,2	NB4	blood:
38	chr2:151966049..151968023-chr2:151983084..151984640,2	MCF-7	breast:
39	chr2:151913690..151917592-chr2:151920463..151923013,3	K562	blood:
40	chr2:151718532..151720265-chr2:151722000..151724171,2	K562	blood:
41	chr2:151768362..151769212-chr2:151907879..151908719,2	MCF-7	breast:
42	chr2:152033034..152033617-chr2:152201109..152202082,2	MCF-7	breast:
43	chr2:151834278..151835808-chr2:151846430..151849245,2	K562	blood:
44	chr2:151868019..151872391-chr2:151872649..151877183,5	K562	blood:
45	chr2:151911293..151912869-chr2:151915243..151918186,2	K562	blood:
46	chr2:152010696..152012482-chr2:152014906..152017450,2	K562	blood:
47	chr2:151867304..151868964-chr2:151869029..151870769,2	MCF-7	breast:
48	chr2:151918025..151920137-chr2:151922647..151924328,2	K562	blood:
49	chr2:151999581..152002485-chr2:152004385..152006033,2	K562	blood:
50	chr2:151999683..152001762-chr2:152019271..152021804,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNFAIP6-1	chr2:151839020-151839029	XLOC_001708
2	lnc-TNFAIP6-1	chr2:151851678-151851778	XLOC_001708
3	lnc-AC023469.1.1-1	chr2:151812105-151812299	NONHSAT074946
4	lnc-AC023469.1.1-1	chr2:151812442-151812560	NONHSAT074946
5	lnc-RBM43-1	chr2:151991218-151991283	ENSG00000236885
6	lnc-RBM43-1	chr2:151974469-151974888	ENSG00000236885
7	lnc-RBM43-1	chr2:152042634-152042723	ENSG00000236885
8	lnc-TNFAIP6-1	chr2:151849861-151850021	XLOC_001708
9	lnc-TNFAIP6-1	chr2:151859604-151859988	XLOC_001708

No data

Variant related genes	Relation type
FABP5P10	TF binding region
ENSG00000222031	TF binding region
ENSG00000236885	TF binding region
ENSG00000228064	TF binding region
FABP5P10	CpG island
ENSG00000222031	CpG island
ENSG00000236885	CpG island
ENSG00000228064	CpG island
ENSG00000115963	chromatin interactions
ENSG00000207270	chromatin interactions
TRIM59	miRNA target sites
F3	miRNA target sites
ARID4B	miRNA target sites

Extended variants
information (count: 11136 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:11136 , 50 per page) page: 1 2 3 4 5 6 7 ... 223

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7579851	chr2:151711700-151711701	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558005387	chr2:151711718-151711719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs7567736	chr2:151711749-151711750	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs34809066	chr2:151711759-151711760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556229613	chr2:151711778-151711779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143630764	chr2:151711782-151711783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148084710	chr2:151711819-151711820	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs555106303	chr2:151711829-151711830	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs192336918	chr2:151711860-151711861	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs58234421	chr2:151711874-151711875	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs114443107	chr2:151711927-151711928	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs116621743	chr2:151711987-151711988	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs141865194	chr2:151711991-151711992	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs150792405	chr2:151711992-151711993	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs184287365	chr2:151711993-151711994	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs543259353	chr2:151712156-151712157	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs559940227	chr2:151712157-151712158	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs527389661	chr2:151712175-151712176	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs386651636	chr2:151712240-151712241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12476555	chr2:151712243-151712244	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs562506420	chr2:151712253-151712254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12464150	chr2:151712272-151712273	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs190456580	chr2:151712276-151712277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76318281	chr2:151712285-151712286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535340238	chr2:151712342-151712343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551369333	chr2:151712354-151712355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555149125	chr2:151712357-151712358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs12472472	chr2:151712393-151712394	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs534809850	chr2:151712424-151712425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558017923	chr2:151712461-151712462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138159401	chr2:151712483-151712484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12472499	chr2:151712494-151712495	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs73967458	chr2:151712550-151712551	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs181838431	chr2:151712588-151712589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543302338	chr2:151712607-151712608	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs560078392	chr2:151712619-151712620	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs112159130	chr2:151712642-151712643	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs545560759	chr2:151712693-151712694	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs549167863	chr2:151712714-151712715	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs79392579	chr2:151712826-151712827	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs549385028	chr2:151712836-151712837	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs142526823	chr2:151712862-151712863	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs146007308	chr2:151712871-151712872	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs375127657	chr2:151712916-151712917	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs376922306	chr2:151712939-151712940	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs186212721	chr2:151712963-151712964	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs567454206	chr2:151713037-151713038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534545775	chr2:151713051-151713052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs536408484	chr2:151713102-151713103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs571666392	chr2:151713127-151713128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	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
epilepsy	18472482	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
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19156171	CNVD
Acute myeloid leukemia	18000384	CNVD
Autism	20808228	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1316 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:151706600-151715800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr2:151707200-151711800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr2:151710200-151722200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr2:151710400-151714800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr2:151710600-151714800	Weak transcription	Fetal Stomach	stomach
6	chr2:151710600-151715000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr2:151711800-151712200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
8	chr2:151712600-151713000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
9	chr2:151713000-151714000	Enhancers	NHEK	skin
10	chr2:151713000-151714600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr2:151713000-151716400	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr2:151713200-151713400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
13	chr2:151713200-151713600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr2:151713200-151713600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr2:151713400-151715800	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr2:151713600-151715600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr2:151713600-151715800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr2:151714000-151715600	Weak transcription	NHEK	skin
19	chr2:151714600-151715600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr2:151714800-151715200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr2:151714800-151715200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr2:151714800-151715200	Enhancers	Fetal Stomach	stomach
23	chr2:151714800-151717200	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr2:151715000-151715400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr2:151715000-151717000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr2:151715000-151717000	Enhancers	Liver	Liver
27	chr2:151715200-151716200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr2:151715200-151716400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr2:151715400-151716400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr2:151715600-151716000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr2:151715600-151716600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr2:151715600-151716600	Enhancers	NHEK	skin
33	chr2:151715800-151716000	Enhancers	HMEC	breast
34	chr2:151715800-151716600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr2:151715800-151717000	Enhancers	H1 Cell Line	embryonic stem cell
36	chr2:151715800-151717000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr2:151715800-151717200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr2:151715800-151717600	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr2:151716000-151717000	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr2:151716000-151717000	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr2:151716000-151717000	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr2:151716000-151717200	Enhancers	H9 Cell Line	embryonic stem cell
43	chr2:151716200-151717200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr2:151716200-151717200	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr2:151716200-151717400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr2:151716200-151717600	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr2:151716400-151716800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr2:151716400-151717000	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr2:151716400-151717000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr2:151716400-151717200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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