Variant report

Variant	nsv584699
Chromosome Location	chr2:234182240-234255547
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:734)
CpG islands
(count:1099)
Chromatin interactive
region (count:64)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:234253215-234253281	HepG2	liver:	n/a	n/a
2	ATF1	chr2:234240092-234240557	K562	blood:	n/a	n/a
3	ATF1	chr2:234238189-234238464	K562	blood:	n/a	n/a
4	ATF2	chr2:234240009-234240623	GM12878	blood:	n/a	n/a
5	ATF2	chr2:234238252-234238772	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr2:234238270-234238799	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr2:234215400-234215626	GM12878	blood:	n/a	n/a
8	BCL11A	chr2:234238414-234238596	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr2:234238350-234238714	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr2:234247428-234247832	GM12878	blood:	n/a	chr2:234247800-234247809
11	BCL3	chr2:234206938-234207242	GM12878	blood:	n/a	n/a
12	BCL3	chr2:234247534-234247800	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:234239999-234240571	GM12878	blood:	n/a	n/a
14	BHLHE40	chr2:234246726-234247173	K562	blood:	n/a	n/a
15	BHLHE40	chr2:234245462-234245472	HepG2	liver:	n/a	n/a
16	BHLHE40	chr2:234242708-234242953	K562	blood:	n/a	n/a
17	BHLHE40	chr2:234251886-234252089	K562	blood:	n/a	n/a
18	CBX3	chr2:234249935-234250238	K562	blood:	n/a	n/a
19	CEBPB	chr2:234252080-234252295	Hela-S3	cervix:	n/a	chr2:234252160-234252171
20	CEBPB	chr2:234209138-234209336	Hela-S3	cervix:	n/a	chr2:234209257-234209268
21	CEBPB	chr2:234197477-234197927	MCF-7	breast:	n/a	chr2:234197712-234197723
22	CEBPB	chr2:234252028-234252313	K562	blood:	n/a	chr2:234252160-234252171
23	CEBPB	chr2:234248144-234248441	IMR90	lung:	n/a	chr2:234248278-234248289
24	CEBPB	chr2:234209182-234209431	A549	lung:	n/a	chr2:234209257-234209268
25	CEBPB	chr2:234251967-234252352	K562	blood:	n/a	chr2:234252160-234252171
26	CEBPB	chr2:234252030-234252306	H1-hESC	embryonic stem cell:	n/a	chr2:234252160-234252171
27	CEBPB	chr2:234238358-234238782	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr2:234248219-234248326	A549	lung:	n/a	chr2:234248278-234248289
29	CEBPB	chr2:234209062-234209400	MCF-7	breast:	n/a	chr2:234209257-234209268
30	CEBPB	chr2:234197702-234197756	HepG2	liver:	n/a	chr2:234197712-234197723
31	CEBPB	chr2:234248065-234248489	Hela-S3	cervix:	n/a	chr2:234248278-234248289
32	CEBPB	chr2:234187050-234187275	A549	lung:	n/a	chr2:234187171-234187182
33	CEBPB	chr2:234209090-234209450	IMR90	lung:	n/a	chr2:234209257-234209268
34	CEBPB	chr2:234216026-234216268	Hela-S3	cervix:	n/a	chr2:234216079-234216090
35	CEBPB	chr2:234251988-234252353	HepG2	liver:	n/a	chr2:234252160-234252171
36	CEBPB	chr2:234205547-234205706	HepG2	liver:	n/a	chr2:234205660-234205671
37	CEBPB	chr2:234252002-234252326	A549	lung:	n/a	chr2:234252160-234252171
38	CEBPB	chr2:234253248-234253262	HepG2	liver:	n/a	n/a
39	CEBPB	chr2:234190988-234191233	A549	lung:	n/a	chr2:234191118-234191129 chr2:234191118-234191131 chr2:234191118-234191131
40	CEBPB	chr2:234209125-234209447	HepG2	liver:	n/a	chr2:234209257-234209268
41	CEBPB	chr2:234248169-234248370	K562	blood:	n/a	chr2:234248278-234248289
42	CEBPB	chr2:234247951-234248452	MCF-7	breast:	n/a	chr2:234248278-234248289
43	CEBPB	chr2:234252055-234252244	K562	blood:	n/a	chr2:234252160-234252171
44	CEBPB	chr2:234187015-234187344	IMR90	lung:	n/a	chr2:234187171-234187182
45	CEBPB	chr2:234248139-234248400	MCF-7	breast:	n/a	chr2:234248278-234248289
46	CEBPB	chr2:234248142-234248419	K562	blood:	n/a	chr2:234248278-234248289
47	CEBPB	chr2:234209239-234209439	K562	blood:	n/a	chr2:234209257-234209268
48	CEBPB	chr2:234197670-234197757	K562	blood:	n/a	chr2:234197712-234197723
49	CEBPB	chr2:234187022-234187342	HepG2	liver:	n/a	chr2:234187171-234187182
50	CEBPB	chr2:234243033-234243113	HepG2	liver:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:234195915-234195965	SK-N-SH_RA	brain:	n/a
2	chr2:234195915-234195965	SK-N-SH_RA	brain:	n/a
3	chr2:234216360-234216410	GM12892	blood:	n/a
4	chr2:234183424-234183474	HMEC	breast:	n/a
5	chr2:234225955-234226005	HUVEC	blood vessel:	n/a
6	chr2:234184376-234184426	AG09309	skin:	n/a
7	chr2:234215965-234216015	NB4	blood:	n/a
8	chr2:234216147-234216197	HRE	kidney:	n/a
9	chr2:234216147-234216197	MCF10A-Er-Src	breast:	n/a
10	chr2:234216562-234216612	SK-N-SH_RA	brain:	n/a
11	chr2:234184279-234184329	AG09309	skin:	n/a
12	chr2:234184376-234184426	AG10803	skin:	n/a
13	chr2:234184279-234184329	NT2-D1	testis:	n/a
14	chr2:234238201-234238251	AG04449	skin:	fetal
15	chr2:234208710-234208760	HCT-116	colon:	n/a
16	chr2:234216147-234216197	NHBE	bronchial:	n/a
17	chr2:234216050-234216100	T-47D	breast:	n/a
18	chr2:234184376-234184426	HIPEpiC	eye:	n/a
19	chr2:234215965-234216015	ovcar-3	ovarian:	n/a
20	chr2:234197367-234197417	NB4	blood:	n/a
21	chr2:234208710-234208760	Jurkat	blood:	n/a
22	chr2:234184376-234184426	NH-A	brain:	n/a
23	chr2:234196709-234196759	GM19239	blood:	n/a
24	chr2:234225955-234226005	HPAEpiC	pulmonary alveolar:	n/a
25	chr2:234225955-234226005	GM19239	blood:	n/a
26	chr2:234216562-234216612	CMK	blood:	n/a
27	chr2:234216050-234216100	NT2-D1	testis:	n/a
28	chr2:234215965-234216015	NT2-D1	testis:	n/a
29	chr2:234197367-234197417	GM19239	blood:	n/a
30	chr2:234216562-234216612	HCT-116	colon:	n/a
31	chr2:234208710-234208760	GM12891	blood:	n/a
32	chr2:234216360-234216410	NHDF-neo	bronchial:	n/a
33	chr2:234184279-234184329	HRE	kidney:	n/a
34	chr2:234238201-234238251	HCPEpiC	choroid plexus:	n/a
35	chr2:234208710-234208760	LNCaP	prostate:	n/a
36	chr2:234184376-234184426	SK-N-SH_RA	brain:	n/a
37	chr2:234183424-234183474	SK-N-MC	brain:	n/a
38	chr2:234225955-234226005	HNPCEpiC	eye:	n/a
39	chr2:234238201-234238251	BE2_C	brain:	n/a
40	chr2:234216050-234216100	BJ	skin:	n/a
41	chr2:234238201-234238251	Caco-2	colon:	n/a
42	chr2:234195915-234195965	H1-hESC	embryonic stem cell:	embryo
43	chr2:234203377-234203427	NB4	blood:	n/a
44	chr2:234216147-234216197	HUVEC	blood vessel:	n/a
45	chr2:234208710-234208760	HCF	heart:	n/a
46	chr2:234225955-234226005	AG04450	lung:	fetal
47	chr2:234216360-234216410	RPTEC	kidney:	n/a
48	chr2:234216360-234216410	HRE	kidney:	n/a
49	chr2:234216360-234216410	H1-hESC	embryonic stem cell:	embryo
50	chr2:234196709-234196759	HL-60	blood:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:234193437..234196062-chr2:234199824..234202606,2	K562	blood:
2	chr2:234243950..234246353-chr2:234247665..234249180,2	K562	blood:
3	chr2:234201699..234203441-chr2:234207264..234209148,2	K562	blood:
4	chr2:234248205..234248729-chr2:234257674..234258176,2	MCF-7	breast:
5	chr2:234216148..234218067-chr2:234242398..234244264,2	MCF-7	breast:
6	chr2:234179437..234182271-chr2:234185909..234188121,2	MCF-7	breast:
7	chr2:234206031..234207757-chr2:234262903..234264733,2	MCF-7	breast:
8	chr2:234159356..234161467-chr2:234246206..234249085,2	MCF-7	breast:
9	chr2:234160050..234162260-chr2:234194203..234196902,2	MCF-7	breast:
10	chr2:234184025..234186339-chr2:234195161..234196726,2	MCF-7	breast:
11	chr2:234200910..234203071-chr2:234204353..234205943,2	MCF-7	breast:
12	chr2:234242293..234245038-chr2:234245423..234247780,3	MCF-7	breast:
13	chr2:234180075..234182326-chr2:234188683..234190200,2	MCF-7	breast:
14	chr2:234198572..234200432-chr2:234205905..234208256,2	MCF-7	breast:
15	chr2:234182703..234184602-chr2:234186866..234188960,2	K562	blood:
16	chr2:234196980..234199300-chr2:234206108..234208506,2	MCF-7	breast:
17	chr2:234182703..234185905-chr2:234186252..234191203,5	K562	blood:
18	chr2:234193437..234196062-chr2:234199824..234202606,2	K562	blood:
19	chr2:234242293..234245038-chr2:234245423..234247780,3	MCF-7	breast:
20	chr2:234159075..234160799-chr2:234195887..234199490,3	MCF-7	breast:
21	chr2:234216005..234218418-chr2:234218619..234221602,2	MCF-7	breast:
22	chr2:234209576..234212564-chr2:234237690..234239510,2	MCF-7	breast:
23	chr2:234197481..234200448-chr2:234203649..234206095,3	MCF-7	breast:
24	chr2:234198551..234200102-chr2:234262598..234264638,2	MCF-7	breast:
25	chr2:234223100..234224098-chr2:234259138..234259923,2	MCF-7	breast:
26	chr2:234216148..234218067-chr2:234242398..234244264,2	MCF-7	breast:
27	chr2:234179437..234182271-chr2:234185909..234188121,2	MCF-7	breast:
28	chr2:234205572..234208233-chr2:234208734..234211089,2	K562	blood:
29	chr2:234236421..234239312-chr2:234248555..234251486,2	K562	blood:
30	chr2:234252596..234255070-chr2:234259544..234261790,2	MCF-7	breast:
31	chr2:234200856..234204903-chr2:234205910..234207803,3	MCF-7	breast:
32	chr2:234226679..234228246-chr2:234234524..234237366,2	K562	blood:
33	chr2:234244512..234246230-chr2:234262489..234264948,2	MCF-7	breast:
34	chr2:234245499..234247293-chr2:234261946..234264130,2	K562	blood:
35	chr2:234201699..234203441-chr2:234207264..234209148,2	K562	blood:
36	chr2:234238740..234240381-chr2:234244254..234246759,2	MCF-7	breast:
37	chr2:234157580..234161544-chr2:234185934..234189119,3	K562	blood:
38	chr2:234187699..234192126-chr2:234193639..234199355,9	MCF-7	breast:
39	chr2:234193121..234195038-chr2:234197728..234199458,2	K562	blood:
40	chr2:234237506..234239939-chr2:234241158..234243320,2	K562	blood:
41	chr2:234205572..234208233-chr2:234208734..234211089,2	K562	blood:
42	chr2:234195943..234198419-chr2:234201590..234203140,2	MCF-7	breast:
43	chr2:234226679..234228246-chr2:234234524..234237366,2	K562	blood:
44	chr2:234232608..234233132-chr2:234262796..234263472,2	MCF-7	breast:
45	chr2:234177414..234182460-chr2:234196864..234199879,7	MCF-7	breast:
46	chr2:234253774..234256883-chr2:234262038..234267744,5	K562	blood:
47	chr2:234190427..234194306-chr2:234194807..234197330,3	MCF-7	breast:
48	chr2:234178234..234182601-chr2:234261429..234266540,8	MCF-7	breast:
49	chr2:234180075..234182326-chr2:234188683..234190200,2	MCF-7	breast:
50	chr2:234206531..234209535-chr2:234260932..234264181,3	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SAG-4	chr2:234184372-234184649	NONHSAT077462
2	lnc-ATG16L1-3	chr2:234229276-234229370	NONHSAT077476
3	lnc-ATG16L1-1	chr2:234207098-234207584	NONHSAT077470
4	lnc-USP40-3	chr2:234205814-234206210	NONHSAT077469
5	lnc-ATG16L1-3	chr2:234224722-234224799	NONHSAT077471
6	lnc-ATG16L1-3	chr2:234228194-234228669	NONHSAT077476
7	lnc-ATG16L1-3	chr2:234216463-234216668	NONHSAT077471

No data

Variant related genes	Relation type
SAG	TF binding region
SCARNA5	TF binding region
ATG16L1	TF binding region
SCARNA6	TF binding region
SAG	CpG island
SCARNA5	CpG island
ATG16L1	CpG island
SCARNA6	CpG island
ENSG00000259793	chromatin interactions
ENSG00000252010	chromatin interactions
ENSG00000130561	chromatin interactions
ENSG00000251791	chromatin interactions
ENSG00000077044	chromatin interactions
ENSG00000243637	chromatin interactions
ENSG00000085978	chromatin interactions

Extended variants
information (count: 3197 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:3197 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2289472	chr2:234182240-234182241	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs538990936	chr2:234182276-234182277	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs199558257	chr2:234182335-234182336	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs569382385	chr2:234182338-234182339	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs372958037	chr2:234182356-234182357	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs201415775	chr2:234182376-234182377	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs558116998	chr2:234182427-234182428	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs538445839	chr2:234182457-234182458	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs202032029	chr2:234182464-234182465	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs201424939	chr2:234182473-234182474	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs528334979	chr2:234182497-234182498	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs573781731	chr2:234182567-234182568	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs542604072	chr2:234182604-234182605	Strong transcription Weak transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs553042730	chr2:234182606-234182607	Strong transcription Weak transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs528429008	chr2:234182610-234182611	Strong transcription Weak transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs114509633	chr2:234182618-234182619	Strong transcription Weak transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs545003258	chr2:234182643-234182644	Strong transcription Weak transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs551897739	chr2:234182667-234182668	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565076810	chr2:234182679-234182680	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs530585966	chr2:234182694-234182695	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs548086211	chr2:234182711-234182712	Strong transcription Weak transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs140476598	chr2:234182729-234182730	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs530145512	chr2:234182743-234182744	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs150010037	chr2:234182753-234182754	Strong transcription Weak transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs530757301	chr2:234182754-234182755	Strong transcription Weak transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs145165552	chr2:234182785-234182786	Strong transcription Weak transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs35563046	chr2:234182800-234182801	Strong transcription Weak transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs552557894	chr2:234182861-234182862	Strong transcription Weak transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs569553985	chr2:234182865-234182866	Strong transcription Weak transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs186232048	chr2:234182960-234182961	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs73998326	chr2:234182963-234182964	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs142349322	chr2:234182983-234182984	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs112942375	chr2:234183002-234183003	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs536398287	chr2:234183037-234183038	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs552981406	chr2:234183041-234183042	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369456895	chr2:234183044-234183045	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs370619293	chr2:234183055-234183056	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189546223	chr2:234183109-234183110	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538643696	chr2:234183116-234183117	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs558545486	chr2:234183121-234183122	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs113960491	chr2:234183150-234183151	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs111819481	chr2:234183156-234183157	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs372958664	chr2:234183209-234183210	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560791185	chr2:234183269-234183270	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370114779	chr2:234183290-234183291	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181428468	chr2:234183292-234183293	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373861966	chr2:234183304-234183305	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs367985149	chr2:234183318-234183319	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112572627	chr2:234183325-234183326	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs147657453	chr2:234183327-234183328	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	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
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	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
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	22429812	CNVD
Bladder cancer	21909424	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
prenatal diagnosis	22389664	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mental retardation	20152051	CNVD
Cancer	21183584	CNVD
Albright''s disease	22277900	CNVD
Brachydactyly-Mental Retardation Syndrome	22470819	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Colorectal cancer	19359472	CNVD
Autism	18414403	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1035 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234162200-234205200	Strong transcription	HUES48 Cell Line	embryonic stem cell
2	chr2:234162200-234205200	Strong transcription	Fetal Muscle Trunk	muscle
3	chr2:234162400-234192000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
4	chr2:234162400-234196400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr2:234162400-234205200	Strong transcription	H1 Cell Line	embryonic stem cell
6	chr2:234162400-234205400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:234162600-234188600	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr2:234162600-234192400	Strong transcription	Osteobl	bone
9	chr2:234162600-234205000	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr2:234162600-234205200	Strong transcription	Fetal Muscle Leg	muscle
11	chr2:234162800-234194000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr2:234162800-234197000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr2:234162800-234205600	Strong transcription	HUES64 Cell Line	embryonic stem cell
14	chr2:234163000-234192200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
15	chr2:234163000-234192200	Strong transcription	Rectal Mucosa Donor 29	rectum
16	chr2:234163200-234188000	Strong transcription	Stomach Smooth Muscle	stomach
17	chr2:234163200-234188800	Strong transcription	Duodenum Mucosa	Duodenum
18	chr2:234163200-234206000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr2:234163800-234188600	Strong transcription	Primary neutrophils fromperipheralblood	blood
20	chr2:234163800-234189000	Strong transcription	Rectal Mucosa Donor 31	rectum
21	chr2:234164200-234205400	Strong transcription	HUES6 Cell Line	embryonic stem cell
22	chr2:234164200-234205400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr2:234164400-234192000	Strong transcription	NH-A	brain
24	chr2:234164400-234196800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr2:234164400-234197200	Strong transcription	Adipose Nuclei	Adipose
26	chr2:234164600-234190400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr2:234164600-234192000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr2:234164600-234192200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr2:234164600-234206000	Strong transcription	HepG2	liver
30	chr2:234164800-234195800	Strong transcription	Fetal Intestine Large	intestine
31	chr2:234165000-234192200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr2:234165000-234206000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr2:234165200-234205400	Strong transcription	Sigmoid Colon	Sigmoid Colon
34	chr2:234165400-234192000	Strong transcription	Brain Cingulate Gyrus	brain
35	chr2:234166200-234191800	Strong transcription	H9 Cell Line	embryonic stem cell
36	chr2:234166600-234189000	Strong transcription	Duodenum Smooth Muscle	Duodenum
37	chr2:234166800-234206000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
38	chr2:234169000-234185200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr2:234169400-234197200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr2:234169800-234192000	Strong transcription	Skeletal Muscle Female	skeletal muscle
41	chr2:234171200-234191800	Strong transcription	HSMM	muscle
42	chr2:234172200-234204800	Strong transcription	Placenta	Placenta
43	chr2:234173000-234186000	Weak transcription	Fetal Heart	heart
44	chr2:234174000-234196000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr2:234176400-234187400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr2:234176800-234207800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr2:234177000-234182600	Weak transcription	NHLF	lung
48	chr2:234177000-234206000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
49	chr2:234177200-234192000	Strong transcription	HMEC	breast
50	chr2:234177200-234205400	Strong transcription	Dnd41	blood

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