Variant report

Variant	nsv1005183
Chromosome Location	chr1:77728990-77949309
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1548)
CpG islands
(count:1712)
Chromatin interactive
region (count:61)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1548 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:77813327-77813667	K562	blood:	n/a	n/a
2	ARID3A	chr1:77882857-77883087	K562	blood:	n/a	n/a
3	ATF1	chr1:77830671-77830692	K562	blood:	n/a	n/a
4	ATF2	chr1:77879101-77879603	GM12878	blood:	n/a	n/a
5	ATF3	chr1:77877807-77878020	K562	blood:	n/a	n/a
6	ATF3	chr1:77787754-77788305	A549	lung:	n/a	n/a
7	ATF3	chr1:77778145-77778418	K562	blood:	n/a	n/a
8	BACH1	chr1:77813415-77813800	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr1:77813423-77813744	K562	blood:	n/a	n/a
10	BACH1	chr1:77864226-77864264	K562	blood:	n/a	n/a
11	BACH1	chr1:77748549-77748670	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr1:77787997-77788456	K562	blood:	n/a	n/a
13	BACH1	chr1:77837156-77837175	K562	blood:	n/a	n/a
14	BACH1	chr1:77748108-77748232	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr1:77747342-77747539	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr1:77902445-77902509	K562	blood:	n/a	n/a
17	BACH1	chr1:77787933-77788535	H1-hESC	embryonic stem cell:	n/a	chr1:77787972-77787986
18	BATF	chr1:77879608-77879958	GM12878	blood:	n/a	n/a
19	BATF	chr1:77879612-77879986	GM12878	blood:	n/a	n/a
20	BCL3	chr1:77787565-77788341	A549	lung:	n/a	chr1:77788127-77788136
21	BCL3	chr1:77813213-77813839	A549	lung:	n/a	chr1:77813605-77813614
22	BHLHE40	chr1:77879247-77879501	GM12878	blood:	n/a	n/a
23	BHLHE40	chr1:77882767-77882967	K562	blood:	n/a	n/a
24	BHLHE40	chr1:77815799-77816266	K562	blood:	n/a	n/a
25	BHLHE40	chr1:77752204-77752272	K562	blood:	n/a	n/a
26	BHLHE40	chr1:77779315-77779411	K562	blood:	n/a	n/a
27	BRCA1	chr1:77935099-77935234	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr1:77813305-77813812	K562	blood:	n/a	n/a
29	CCNT2	chr1:77864936-77865301	K562	blood:	n/a	n/a
30	CEBPB	chr1:77811370-77811493	A549	lung:	n/a	n/a
31	CEBPB	chr1:77839430-77839705	K562	blood:	n/a	chr1:77839576-77839585 chr1:77839576-77839585 chr1:77839576-77839585 chr1:77839574-77839585
32	CEBPB	chr1:77753982-77754330	IMR90	lung:	n/a	n/a
33	CEBPB	chr1:77839393-77839749	HepG2	liver:	n/a	chr1:77839576-77839585 chr1:77839576-77839585 chr1:77839576-77839585 chr1:77839574-77839585
34	CEBPB	chr1:77763893-77764109	HepG2	liver:	n/a	chr1:77764019-77764032 chr1:77764020-77764031
35	CEBPB	chr1:77898338-77898655	IMR90	lung:	n/a	chr1:77898501-77898512
36	CEBPB	chr1:77839392-77839770	IMR90	lung:	n/a	chr1:77839576-77839585 chr1:77839576-77839585 chr1:77839576-77839585 chr1:77839574-77839585
37	CEBPB	chr1:77848039-77848324	A549	lung:	n/a	n/a
38	CEBPB	chr1:77877746-77878082	K562	blood:	n/a	chr1:77877923-77877934
39	CEBPB	chr1:77854372-77854695	IMR90	lung:	n/a	chr1:77854542-77854559
40	CEBPB	chr1:77787734-77788511	HCT-116	colon:	n/a	n/a
41	CEBPB	chr1:77787505-77788395	A549	lung:	n/a	n/a
42	CEBPB	chr1:77877783-77878124	MCF-7	breast:	n/a	chr1:77877923-77877934
43	CEBPB	chr1:77864115-77864182	K562	blood:	n/a	chr1:77864163-77864174
44	CEBPB	chr1:77739578-77739946	Hela-S3	cervix:	n/a	chr1:77739754-77739765
45	CEBPB	chr1:77739613-77739943	K562	blood:	n/a	chr1:77739754-77739765
46	CEBPB	chr1:77763940-77764057	IMR90	lung:	n/a	chr1:77764019-77764032 chr1:77764020-77764031
47	CEBPB	chr1:77896726-77897014	IMR90	lung:	n/a	n/a
48	CEBPB	chr1:77753228-77753428	K562	blood:	n/a	n/a
49	CEBPB	chr1:77877786-77878085	H1-hESC	embryonic stem cell:	n/a	chr1:77877923-77877934
50	CEBPB	chr1:77787675-77788246	IMR90	lung:	n/a	n/a

(count:1712 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:77912654-77912704	BE2_C	brain:	n/a
2	chr1:77748221-77748271	NHBE	bronchial:	n/a
3	chr1:77836400-77836450	HCM	heart:	n/a
4	chr1:77748391-77748441	GM12891	blood:	n/a
5	chr1:77912654-77912704	BE2_C	brain:	n/a
6	chr1:77748221-77748271	NHBE	bronchial:	n/a
7	chr1:77836400-77836450	HCM	heart:	n/a
8	chr1:77748391-77748441	GM12891	blood:	n/a
9	chr1:77747374-77747424	CMK	blood:	n/a
10	chr1:77747382-77747432	MCF10A-Er-Src	breast:	n/a
11	chr1:77747374-77747424	BE2_C	brain:	n/a
12	chr1:77933593-77933643	RPTEC	kidney:	n/a
13	chr1:77747875-77747925	K562	blood:	n/a
14	chr1:77747387-77747437	K562	blood:	n/a
15	chr1:77747374-77747424	AG04450	lung:	fetal
16	chr1:77748325-77748375	AoSMC	blood vessel:	n/a
17	chr1:77912654-77912704	NH-A	brain:	n/a
18	chr1:77836400-77836450	HEEpiC	esophagus:	n/a
19	chr1:77748221-77748271	HNPCEpiC	eye:	n/a
20	chr1:77788391-77788441	AG10803	skin:	n/a
21	chr1:77748728-77748778	Jurkat	blood:	n/a
22	chr1:77746571-77746621	HL-60	blood:	n/a
23	chr1:77747987-77748037	Hepatocyte	liver:	n/a
24	chr1:77747987-77748037	HepG2	liver:	n/a
25	chr1:77748480-77748530	HMEC	breast:	n/a
26	chr1:77746571-77746621	MCF-7	breast:	n/a
27	chr1:77904032-77904082	HRE	kidney:	n/a
28	chr1:77904032-77904082	HUVEC	blood vessel:	n/a
29	chr1:77730341-77730391	NHBE	bronchial:	n/a
30	chr1:77748325-77748375	HUVEC	blood vessel:	n/a
31	chr1:77748129-77748179	GM12878	blood:	n/a
32	chr1:77940194-77940244	HNPCEpiC	eye:	n/a
33	chr1:77912654-77912704	H1-hESC	embryonic stem cell:	embryo
34	chr1:77748190-77748240	HCPEpiC	choroid plexus:	n/a
35	chr1:77879031-77879081	ECC-1	luminal epithelium:	n/a
36	chr1:77747374-77747424	ECC-1	luminal epithelium:	n/a
37	chr1:77747987-77748037	AG04449	skin:	fetal
38	chr1:77940194-77940244	BJ	skin:	n/a
39	chr1:77768670-77768720	NB4	blood:	n/a
40	chr1:77912654-77912704	HAEpiC	amniotic membrane:	n/a
41	chr1:77933593-77933643	LNCaP	prostate:	n/a
42	chr1:77744527-77744577	GM19239	blood:	n/a
43	chr1:77748325-77748375	HRE	kidney:	n/a
44	chr1:77746571-77746621	SK-N-MC	brain:	n/a
45	chr1:77730341-77730391	Hela-S3	cervix:	n/a
46	chr1:77747875-77747925	SAEC	small airway:	n/a
47	chr1:77751443-77751493	A549	lung:	n/a
48	chr1:77744527-77744577	ovcar-3	ovarian:	n/a
49	chr1:77746028-77746078	AG09319	gingival:	n/a
50	chr1:77768670-77768720	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:77898654..77900844-chr1:77900858..77902632,2	K562	blood:
2	chr1:77773875..77776592-chr1:77778401..77780393,2	K562	blood:
3	chr1:77838249..77841580-chr1:77844120..77846924,3	K562	blood:
4	chr1:77922521..77925013-chr1:77930694..77933146,2	K562	blood:
5	chr1:77781240..77784199-chr1:77786063..77789429,3	K562	blood:
6	chr1:77813535..77817247-chr1:77819129..77821661,3	K562	blood:
7	chr1:77786657..77790465-chr1:77794165..77797983,5	K562	blood:
8	chr1:77922521..77925013-chr1:77930694..77933146,2	K562	blood:
9	chr1:77931036..77935396-chr1:77935652..77939462,4	K562	blood:
10	chr1:77808952..77811153-chr1:77811889..77814837,3	K562	blood:
11	chr1:77915846..77918627-chr1:77942564..77944973,2	K562	blood:
12	chr1:77840080..77842951-chr1:77843079..77845956,2	K562	blood:
13	chr1:77803574..77805696-chr1:77808373..77811184,2	K562	blood:
14	chr1:77734487..77736181-chr1:77737477..77740179,2	K562	blood:
15	chr1:77820213..77822574-chr1:77837980..77839971,2	K562	blood:
16	chr1:77781240..77784199-chr1:77786063..77789429,3	K562	blood:
17	chr1:77817387..77819700-chr1:77829412..77831526,2	K562	blood:
18	chr1:77948475..77951287-chr1:77952444..77954143,2	K562	blood:
19	chr1:77863743..77865980-chr1:77869588..77871346,2	MCF-7	breast:
20	chr1:77753173..77754991-chr1:77758287..77760412,2	K562	blood:
21	chr1:77684670..77686781-chr1:77746398..77749229,3	MCF-7	breast:
22	chr1:77931036..77935396-chr1:77935652..77939462,4	K562	blood:
23	chr1:77773875..77776592-chr1:77778401..77780393,2	K562	blood:
24	chr1:77884906..77887618-chr1:77887940..77890792,2	K562	blood:
25	chr1:77879822..77883300-chr1:77884323..77886627,3	K562	blood:
26	chr1:77817387..77819700-chr1:77829412..77831526,2	K562	blood:
27	chr1:77613856..77614476-chr1:77778903..77779788,3	MCF-7	breast:
28	chr1:77863743..77865980-chr1:77869588..77871346,2	MCF-7	breast:
29	chr1:77766400..77769347-chr1:77774174..77776470,2	K562	blood:
30	chr1:77800850..77802906-chr1:77808839..77811441,2	K562	blood:
31	chr1:77800850..77802906-chr1:77808839..77811441,2	K562	blood:
32	chr1:77921275..77923529-chr1:77924808..77927657,2	K562	blood:
33	chr1:77786657..77790465-chr1:77794165..77797983,5	K562	blood:
34	chr1:77930945..77932536-chr1:77935599..77937713,2	K562	blood:
35	chr1:77925586..77927133-chr1:77930650..77932408,2	K562	blood:
36	chr1:77930945..77932536-chr1:77935599..77937713,2	K562	blood:
37	chr1:77921085..77922775-chr1:77926149..77927657,2	K562	blood:
38	chr1:77734487..77736181-chr1:77737477..77740179,2	K562	blood:
39	chr1:77725962..77727892-chr1:77729929..77731695,2	K562	blood:
40	chr1:77808952..77811153-chr1:77811889..77814837,3	K562	blood:
41	chr1:77848625..77851388-chr1:77856046..77857878,2	K562	blood:
42	chr1:77820213..77822574-chr1:77837980..77839971,2	K562	blood:
43	chr1:77742540..77744145-chr1:77750069..77752259,2	K562	blood:
44	chr1:77838249..77841580-chr1:77844120..77846924,3	K562	blood:
45	chr1:77813619..77816574-chr1:78468319..78470340,2	K562	blood:
46	chr1:77744169..77746110-chr1:77748254..77750712,2	K562	blood:
47	chr1:77925586..77927133-chr1:77930650..77932408,2	K562	blood:
48	chr1:77915846..77918627-chr1:77942564..77944973,2	K562	blood:
49	chr1:77684347..77685329-chr1:77778972..77779827,3	MCF-7	breast:
50	chr1:77921275..77923529-chr1:77924808..77927657,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PIGK-1	chr1:77815115-77815270	ENSG00000233099.1
2	lnc-PIGK-1	chr1:77811731-77811951	ENSG00000233099.1

No data

Variant related genes	Relation type
ENSG00000221664	TF binding region
RNU7-8P	TF binding region
ENSG00000233099	TF binding region
AK5	TF binding region
ENSG00000221664	CpG island
RNU7-8P	CpG island
ENSG00000233099	CpG island
AK5	CpG island
ENSG00000221664	chromatin interactions
ENSG00000233099	chromatin interactions
ENSG00000142892	chromatin interactions
ENSG00000162616	chromatin interactions
ENSG00000273338	chromatin interactions
ENSG00000154027	chromatin interactions
ENSG00000251767	chromatin interactions
ENSG00000036549	chromatin interactions

Extended variants
information (count: 8013 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:8013 , 50 per page) page: 1 2 3 4 5 6 7 ... 161

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568400690	chr1:77729245-77729246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs148588550	chr1:77729293-77729294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547604668	chr1:77729315-77729316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs565915054	chr1:77729366-77729367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532808127	chr1:77729368-77729369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78246870	chr1:77729418-77729419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549761617	chr1:77729440-77729441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs185133719	chr1:77729444-77729445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs576812155	chr1:77729485-77729486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs569651865	chr1:77729507-77729508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs537308049	chr1:77729519-77729520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs12033176	chr1:77729544-77729545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556017439	chr1:77729571-77729572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573583944	chr1:77729572-77729573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs541004791	chr1:77729589-77729590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142959704	chr1:77729590-77729591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs146131362	chr1:77729595-77729596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559744664	chr1:77730615-77730616	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs571165303	chr1:77730765-77730766	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs146452194	chr1:77730812-77730813	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs539743564	chr1:77730816-77730817	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs551952221	chr1:77730819-77730820	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs543537291	chr1:77730839-77730840	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570147331	chr1:77730892-77730893	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs531026527	chr1:77730907-77730908	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs11576574	chr1:77730966-77730967	Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs567866778	chr1:77730984-77730985	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs535280101	chr1:77730992-77730993	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs376676312	chr1:77731001-77731002	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs553239680	chr1:77731009-77731010	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs570955370	chr1:77731010-77731011	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs115319930	chr1:77731019-77731020	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs371312695	chr1:77731030-77731031	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs57002064	chr1:77731031-77731032	Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs140750086	chr1:77731097-77731098	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs554703559	chr1:77731123-77731124	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573065300	chr1:77731151-77731152	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191288390	chr1:77731184-77731185	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs17100100	chr1:77731277-77731278	Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs1988302	chr1:77731287-77731288	Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs577181051	chr1:77732263-77732264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs187828163	chr1:77732270-77732271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs138146513	chr1:77732279-77732280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532466993	chr1:77732297-77732298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs142163788	chr1:77732315-77732316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs545764023	chr1:77732322-77732323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191136957	chr1:77732446-77732447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs373611150	chr1:77732477-77732478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs546757833	chr1:77732528-77732529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs1167221	chr1:77732565-77732566	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:2782 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77729200-77729600	Enhancers	Stomach Mucosa	stomach
2	chr1:77730600-77731200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
3	chr1:77730600-77731200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
4	chr1:77730600-77731400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
5	chr1:77730800-77731000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
6	chr1:77730800-77731200	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
7	chr1:77730800-77731200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr1:77730800-77731200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
9	chr1:77730800-77731200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr1:77730800-77731200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr1:77730800-77731400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
12	chr1:77730800-77731400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:77730800-77731400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr1:77730800-77731400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
15	chr1:77732200-77733600	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr1:77732200-77733800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr1:77732400-77733400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
18	chr1:77732600-77732800	Enhancers	Primary T helper naive cells from peripheral blood	blood
19	chr1:77732600-77733600	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr1:77732800-77733400	Enhancers	Primary T killer memory cells from peripheral blood	blood
21	chr1:77733000-77733400	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr1:77733000-77733400	Enhancers	Primary T cells from cord blood	blood
23	chr1:77733400-77733600	Enhancers	Primary T helper naive cells from peripheral blood	blood
24	chr1:77733400-77735600	Weak transcription	Primary T cells from cord blood	blood
25	chr1:77735400-77735600	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr1:77735600-77735800	Enhancers	Primary T cells from cord blood	blood
27	chr1:77736400-77740600	Enhancers	NHDF-Ad	bronchial
28	chr1:77736600-77738400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr1:77737000-77737200	Enhancers	Aorta	Aorta
30	chr1:77737000-77737400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr1:77737000-77738000	Enhancers	HSMMtube	muscle
32	chr1:77737000-77738200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr1:77737000-77738200	Enhancers	Osteobl	bone
34	chr1:77737000-77738400	Enhancers	Muscle Satellite Cultured Cells	--
35	chr1:77737000-77738400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr1:77737000-77738400	Enhancers	NHLF	lung
37	chr1:77737000-77738800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr1:77737200-77737800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr1:77737200-77738000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr1:77737200-77738400	Enhancers	HSMM	muscle
41	chr1:77737200-77747400	Weak transcription	Aorta	Aorta
42	chr1:77737400-77737800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
43	chr1:77737400-77737800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr1:77737400-77737800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
45	chr1:77737400-77738000	Enhancers	HUVEC	blood vessel
46	chr1:77737400-77738200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr1:77737400-77738400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr1:77737600-77737800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr1:77737800-77738400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr1:77738200-77739400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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