Variant report

Variant	nsv548246
Chromosome Location	chr1:176043797-176136273
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:512)
CpG islands
(count:61)
Chromatin interactive
region (count:53)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:512 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:176118908-176120075	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:176088851-176089016	K562	blood:	n/a	n/a
3	ARID3A	chr1:176116012-176116131	K562	blood:	n/a	n/a
4	ARID3A	chr1:176134858-176135036	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:176088756-176089014	HepG2	liver:	n/a	n/a
6	ATF1	chr1:176102253-176102629	K562	blood:	n/a	n/a
7	ATF1	chr1:176073893-176073944	K562	blood:	n/a	n/a
8	BACH1	chr1:176131786-176131807	K562	blood:	n/a	n/a
9	BATF	chr1:176074944-176075114	GM12878	blood:	n/a	chr1:176075026-176075037
10	BATF	chr1:176065200-176065457	GM12878	blood:	n/a	n/a
11	BATF	chr1:176071886-176072236	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:176065383-176065513	GM12878	blood:	n/a	n/a
13	BRCA1	chr1:176123981-176124018	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr1:176091456-176091851	K562	blood:	n/a	n/a
15	CBX3	chr1:176127072-176127554	K562	blood:	n/a	n/a
16	CBX3	chr1:176067710-176068074	K562	blood:	n/a	n/a
17	CBX3	chr1:176127078-176127574	HCT-116	colon:	n/a	n/a
18	CBX3	chr1:176127053-176127577	K562	blood:	n/a	n/a
19	CBX3	chr1:176067733-176068108	K562	blood:	n/a	n/a
20	CCNT2	chr1:176092050-176092561	K562	blood:	n/a	n/a
21	CEBPB	chr1:176116381-176116645	IMR90	lung:	n/a	n/a
22	CEBPB	chr1:176119462-176119722	A549	lung:	n/a	n/a
23	CEBPB	chr1:176113756-176113962	K562	blood:	n/a	n/a
24	CEBPB	chr1:176061215-176061414	K562	blood:	n/a	n/a
25	CEBPB	chr1:176096388-176096423	K562	blood:	n/a	n/a
26	CEBPB	chr1:176071357-176071654	IMR90	lung:	n/a	n/a
27	CEBPB	chr1:176119450-176119819	HepG2	liver:	n/a	n/a
28	CEBPB	chr1:176088515-176088708	K562	blood:	n/a	chr1:176088642-176088651 chr1:176088642-176088653
29	CEBPB	chr1:176091944-176091969	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr1:176088145-176088820	IMR90	lung:	n/a	chr1:176088642-176088651 chr1:176088642-176088653
31	CEBPB	chr1:176119528-176119700	HepG2	liver:	n/a	n/a
32	CEBPB	chr1:176061126-176061422	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr1:176102543-176102573	K562	blood:	n/a	n/a
34	CHD2	chr1:176068334-176068441	K562	blood:	n/a	n/a
35	CREB1	chr1:176119323-176119919	HepG2	liver:	n/a	n/a
36	CREB1	chr1:176119415-176119924	HepG2	liver:	n/a	n/a
37	CTCF	chr1:176088800-176088950	K562	blood:	n/a	chr1:176088890-176088911 chr1:176088893-176088901 chr1:176088888-176088906
38	CTCF	chr1:176088860-176089010	HRE	kidney:	n/a	chr1:176088890-176088911 chr1:176088893-176088901 chr1:176088888-176088906
39	CTCF	chr1:176088771-176089082	HepG2	liver:	n/a	chr1:176088890-176088911 chr1:176088893-176088901 chr1:176088888-176088906
40	CTCF	chr1:176088762-176089143	MCF-7	breast:	n/a	chr1:176088890-176088911 chr1:176088893-176088901 chr1:176088888-176088906
41	CTCF	chr1:176088800-176088950	GM12871	blood:	n/a	chr1:176088890-176088911 chr1:176088893-176088901 chr1:176088888-176088906
42	CTCF	chr1:176088760-176088910	HMEC	breast:	n/a	chr1:176088893-176088901 chr1:176088888-176088906
43	CTCF	chr1:176088709-176089093	GM12878	blood:	n/a	chr1:176088890-176088911 chr1:176088893-176088901 chr1:176088888-176088906
44	CTCF	chr1:176088880-176089030	HCT-116	colon:	n/a	chr1:176088890-176088911 chr1:176088893-176088901 chr1:176088888-176088906
45	CTCF	chr1:176088840-176088990	GM12878	blood:	n/a	chr1:176088890-176088911 chr1:176088893-176088901 chr1:176088888-176088906
46	CTCF	chr1:176088820-176088970	GM12864	blood:	n/a	chr1:176088890-176088911 chr1:176088893-176088901 chr1:176088888-176088906
47	CTCF	chr1:176088820-176088970	GM12866	blood:	n/a	chr1:176088890-176088911 chr1:176088893-176088901 chr1:176088888-176088906
48	CTCF	chr1:176088900-176089050	A549	lung:	n/a	n/a
49	CTCF	chr1:176088802-176088937	ProgFib	skin:	n/a	chr1:176088890-176088911 chr1:176088893-176088901 chr1:176088888-176088906
50	CTCF	chr1:176088820-176088970	AG10803	skin:	n/a	chr1:176088890-176088911 chr1:176088893-176088901 chr1:176088888-176088906

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:176126003-176126053	HAEpiC	amniotic membrane:	n/a
2	chr1:176126003-176126053	NHBE	bronchial:	n/a
3	chr1:176126003-176126053	ProgFib	skin:	n/a
4	chr1:176126003-176126053	GM12878	blood:	n/a
5	chr1:176126003-176126053	GM12892	blood:	n/a
6	chr1:176126003-176126053	HMEC	breast:	n/a
7	chr1:176126003-176126053	HIPEpiC	eye:	n/a
8	chr1:176126003-176126053	SKMC	muscle:	n/a
9	chr1:176126003-176126053	HEK293	kidney:	embryo
10	chr1:176126003-176126053	AG10803	skin:	n/a
11	chr1:176126003-176126053	SAEC	small airway:	n/a
12	chr1:176126003-176126053	BJ	skin:	n/a
13	chr1:176126003-176126053	H1-hESC	embryonic stem cell:	embryo
14	chr1:176126003-176126053	BE2_C	brain:	n/a
15	chr1:176126003-176126053	AG09319	gingival:	n/a
16	chr1:176126003-176126053	IMR90	lung:	fetal
17	chr1:176126003-176126053	NH-A	brain:	n/a
18	chr1:176126003-176126053	NHDF-neo	bronchial:	n/a
19	chr1:176126003-176126053	SK-N-SH	brain:	n/a
20	chr1:176126003-176126053	RPTEC	kidney:	n/a
21	chr1:176126003-176126053	Caco-2	colon:	n/a
22	chr1:176126003-176126053	HCT-116	colon:	n/a
23	chr1:176126003-176126053	Hepatocyte	liver:	n/a
24	chr1:176126003-176126053	GM06990	blood:	n/a
25	chr1:176126003-176126053	AG04449	skin:	fetal
26	chr1:176126003-176126053	AG04450	lung:	fetal
27	chr1:176126003-176126053	GM19239	blood:	n/a
28	chr1:176126003-176126053	PrEC	prostate:	n/a
29	chr1:176126003-176126053	GM12891	blood:	n/a
30	chr1:176126003-176126053	HUVEC	blood vessel:	n/a
31	chr1:176126003-176126053	SK-N-SH_RA	brain:	n/a
32	chr1:176126003-176126053	HEEpiC	esophagus:	n/a
33	chr1:176126003-176126053	MCF10A-Er-Src	breast:	n/a
34	chr1:176126003-176126053	K562	blood:	n/a
35	chr1:176126003-176126053	HRCEpiC	kidney:	n/a
36	chr1:176126003-176126053	ovcar-3	ovarian:	n/a
37	chr1:176126003-176126053	ECC-1	luminal epithelium:	n/a
38	chr1:176126003-176126053	CMK	blood:	n/a
39	chr1:176126003-176126053	HCPEpiC	choroid plexus:	n/a
40	chr1:176126003-176126053	NB4	blood:	n/a
41	chr1:176126003-176126053	HNPCEpiC	eye:	n/a
42	chr1:176126003-176126053	HPAEpiC	pulmonary alveolar:	n/a
43	chr1:176126003-176126053	AG09309	skin:	n/a
44	chr1:176126003-176126053	MCF-7	breast:	n/a
45	chr1:176126003-176126053	AoSMC	blood vessel:	n/a
46	chr1:176126003-176126053	HCM	heart:	n/a
47	chr1:176126003-176126053	U87	brain:	n/a
48	chr1:176126003-176126053	NT2-D1	testis:	n/a
49	chr1:176126003-176126053	PANC-1	pancreas:	n/a
50	chr1:176126003-176126053	A549	lung:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:176118719..176121398-chr1:176126586..176128691,2	MCF-7	breast:
2	chr1:176092493..176094007-chr1:176098723..176101277,2	MCF-7	breast:
3	chr1:176119104..176121443-chr1:176123713..176126655,2	K562	blood:
4	chr1:176077424..176078957-chr1:176081376..176083249,2	MCF-7	breast:
5	chr1:176087488..176090030-chr1:176090768..176093080,2	K562	blood:
6	chr1:176088496..176089144-chr1:176849852..176850606,2	MCF-7	breast:
7	chr1:176077424..176078957-chr1:176081376..176083249,2	MCF-7	breast:
8	chr1:176098829..176100605-chr1:176104369..176106767,2	MCF-7	breast:
9	chr1:176112849..176115015-chr1:176116534..176118613,2	K562	blood:
10	chr1:176117831..176119910-chr1:176126935..176128982,2	K562	blood:
11	chr1:176090227..176092854-chr1:176094408..176097358,3	MCF-7	breast:
12	chr1:176117831..176119910-chr1:176126935..176128982,2	K562	blood:
13	chr1:176059320..176060876-chr1:176061797..176063897,2	K562	blood:
14	chr1:176071649..176074006-chr1:176077683..176079750,2	K562	blood:
15	chr1:176118719..176121398-chr1:176126586..176128691,2	MCF-7	breast:
16	chr1:176105661..176107653-chr1:176109994..176112277,2	K562	blood:
17	chr1:176132100..176134204-chr1:176136004..176138442,2	MCF-7	breast:
18	chr1:176042309..176045520-chr1:176046203..176049197,3	K562	blood:
19	chr1:176071649..176074006-chr1:176077683..176079750,2	K562	blood:
20	chr1:176118538..176120169-chr1:176174472..176176395,2	MCF-7	breast:
21	chr1:176088244..176089817-chr1:176091101..176092975,2	MCF-7	breast:
22	chr1:176097773..176100235-chr1:176108786..176111266,2	K562	blood:
23	chr1:176082187..176085004-chr1:176089013..176091231,2	K562	blood:
24	chr1:176064570..176066315-chr5:178976272..178977861,2	MCF-7	breast:
25	chr1:176074166..176076778-chr1:176077523..176081005,3	K562	blood:
26	chr1:176059320..176060876-chr1:176061797..176063897,2	K562	blood:
27	chr1:176048905..176051359-chr1:176053995..176056465,2	K562	blood:
28	chr1:176097773..176100235-chr1:176108786..176111266,2	K562	blood:
29	chr1:176074166..176076778-chr1:176077523..176081005,3	K562	blood:
30	chr1:176108785..176110612-chr1:176115277..176116874,2	MCF-7	breast:
31	chr1:176091534..176094018-chr1:176098699..176100256,2	K562	blood:
32	chr1:176088244..176089817-chr1:176091101..176092975,2	MCF-7	breast:
33	chr1:176042309..176045520-chr1:176046203..176049197,3	K562	blood:
34	chr1:176112849..176115015-chr1:176116534..176118613,2	K562	blood:
35	chr1:176105661..176107653-chr1:176109994..176112277,2	K562	blood:
36	chr1:176132100..176134204-chr1:176136004..176138442,2	MCF-7	breast:
37	chr1:176103466..176105125-chr1:176110395..176112776,2	K562	blood:
38	chr1:176117419..176119853-chr1:176175222..176177852,2	MCF-7	breast:
39	chr1:176090227..176092854-chr1:176094408..176097358,3	MCF-7	breast:
40	chr1:176092493..176094007-chr1:176098723..176101277,2	MCF-7	breast:
41	chr1:176108785..176110612-chr1:176115277..176116874,2	MCF-7	breast:
42	chr1:176103163..176105549-chr1:176174911..176176507,2	MCF-7	breast:
43	chr1:176130858..176132751-chr1:176134916..176136520,2	K562	blood:
44	chr1:176109806..176112763-chr1:176116214..176119123,3	K562	blood:
45	chr1:176116758..176118552-chr1:176143991..176146342,2	MCF-7	breast:
46	chr1:176098829..176100605-chr1:176104369..176106767,2	MCF-7	breast:
47	chr1:176124657..176126215-chr1:176175102..176177140,2	K562	blood:
48	chr1:176130858..176132751-chr1:176134916..176136520,2	K562	blood:
49	chr1:176109806..176112763-chr1:176116214..176119123,3	K562	blood:
50	chr1:176119104..176121443-chr1:176123713..176126655,2	K562	blood:

No data

Variant related genes	Relation type
RFWD2	TF binding region
RFWD2	CpG island
ENSG00000176783	chromatin interactions
ENSG00000143207	chromatin interactions
ENSG00000236021	chromatin interactions

Extended variants
information (count: 3465 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:3465 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2502826	chr1:176043797-176043798	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs10753118	chr1:176043802-176043803	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs550643755	chr1:176043848-176043849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs139826959	chr1:176043888-176043889	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs180873548	chr1:176043905-176043906	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs79480972	chr1:176043928-176043929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs202046609	chr1:176043943-176043944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553260567	chr1:176043946-176043947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370317710	chr1:176043955-176043956	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs2481653	chr1:176044121-176044122	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs145351193	chr1:176044193-176044194	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs147271542	chr1:176044199-176044200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552671928	chr1:176044215-176044216	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2502827	chr1:176044217-176044218	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs558215071	chr1:176044219-176044220	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184931506	chr1:176044254-176044255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545995558	chr1:176044256-176044257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559242585	chr1:176044270-176044271	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528373641	chr1:176044295-176044296	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537824741	chr1:176044326-176044327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561388354	chr1:176044341-176044342	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536871265	chr1:176044381-176044382	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140859242	chr1:176044424-176044425	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574415491	chr1:176044449-176044450	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189301660	chr1:176044467-176044468	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs144801445	chr1:176044472-176044473	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547178798	chr1:176044556-176044557	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554289589	chr1:176044557-176044558	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs114405700	chr1:176044613-176044614	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536199445	chr1:176044622-176044623	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552453562	chr1:176044646-176044647	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182038080	chr1:176044699-176044700	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536556843	chr1:176044728-176044729	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553104667	chr1:176044761-176044762	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs151293159	chr1:176044779-176044780	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368648300	chr1:176044814-176044815	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557838380	chr1:176044826-176044827	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs578056813	chr1:176044837-176044838	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540323037	chr1:176044868-176044869	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372818735	chr1:176044869-176044870	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535195502	chr1:176044905-176044906	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs140559719	chr1:176044907-176044908	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561629718	chr1:176044937-176044938	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150051508	chr1:176044948-176044949	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544207834	chr1:176044959-176044960	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563883367	chr1:176045002-176045003	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533052933	chr1:176045026-176045027	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs145409927	chr1:176045054-176045055	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560709185	chr1:176045070-176045071	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545307117	chr1:176045101-176045102	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Mental retardation	17847001	CNVD
Schizophrenia	19805367	CNVD

Chromatin state (count:2162 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:175976800-176046000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr1:175978200-176050600	Weak transcription	Aorta	Aorta
3	chr1:175978400-176069000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr1:175979600-176045400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr1:175994200-176065200	Weak transcription	Psoas Muscle	Psoas
6	chr1:176006000-176045200	Weak transcription	GM12878-XiMat	blood
7	chr1:176006200-176049000	Weak transcription	HSMM	muscle
8	chr1:176007800-176066400	Weak transcription	Fetal Brain Male	brain
9	chr1:176010200-176048000	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr1:176010400-176066000	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr1:176012200-176044800	Weak transcription	Fetal Stomach	stomach
12	chr1:176012200-176045200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr1:176012200-176045200	Weak transcription	Esophagus	oesophagus
14	chr1:176012200-176045200	Weak transcription	Fetal Lung	lung
15	chr1:176012400-176045400	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr1:176012400-176045800	Weak transcription	Brain Hippocampus Middle	brain
17	chr1:176012400-176048200	Weak transcription	Ovary	ovary
18	chr1:176012400-176048200	Weak transcription	Thymus	Thymus
19	chr1:176012400-176062800	Weak transcription	Lung	lung
20	chr1:176012400-176065800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr1:176012800-176047000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr1:176013000-176045000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr1:176014400-176045200	Weak transcription	Primary T cells fromperipheralblood	blood
24	chr1:176021600-176045000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr1:176028000-176045400	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr1:176028200-176045400	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr1:176028200-176048200	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr1:176028200-176079200	Weak transcription	HSMMtube	muscle
29	chr1:176028400-176047200	Weak transcription	A549	lung
30	chr1:176028400-176047800	Weak transcription	Hela-S3	cervix
31	chr1:176028400-176049600	Weak transcription	K562	blood
32	chr1:176028800-176047200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr1:176029600-176048000	Weak transcription	HepG2	liver
34	chr1:176030000-176047400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr1:176030600-176045600	Weak transcription	Primary hematopoietic stem cells	blood
36	chr1:176030800-176048200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr1:176031000-176054000	Weak transcription	NH-A	brain
38	chr1:176032000-176048200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr1:176034600-176045200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr1:176035000-176069800	Weak transcription	NHEK	skin
41	chr1:176035200-176067600	Weak transcription	Colonic Mucosa	Colon
42	chr1:176035400-176066400	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr1:176035400-176067200	Weak transcription	HUVEC	blood vessel
44	chr1:176035600-176046800	Weak transcription	Fetal Thymus	thymus
45	chr1:176036000-176053800	Weak transcription	Placenta	Placenta
46	chr1:176036400-176045200	Weak transcription	Colon Smooth Muscle	Colon
47	chr1:176036600-176049000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr1:176036800-176045800	Weak transcription	Fetal Muscle Trunk	muscle
49	chr1:176037000-176045600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr1:176037000-176048000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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