Variant report

Variant	nsv546943
Chromosome Location	chr1:104067608-104069167
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:480)
CpG islands
(count:732)
Chromatin interactive
region (count:3)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:480 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:104068398-104069159	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:104068425-104069462	K562	blood:	n/a	n/a
3	ATF2	chr1:104068246-104068748	GM12878	blood:	n/a	n/a
4	ATF2	chr1:104068276-104068823	GM12878	blood:	n/a	n/a
5	BATF	chr1:104068947-104069203	GM12878	blood:	n/a	n/a
6	BCLAF1	chr1:104068286-104068884	GM12878	blood:	n/a	n/a
7	BHLHE40	chr1:104067893-104069179	K562	blood:	n/a	n/a
8	BHLHE40	chr1:104068347-104069164	GM12878	blood:	n/a	n/a
9	BRCA1	chr1:104068338-104068741	HepG2	liver:	n/a	chr1:104068541-104068550
10	BRCA1	chr1:104068332-104068755	H1-hESC	embryonic stem cell:	n/a	chr1:104068541-104068550
11	BRCA1	chr1:104068347-104068826	GM12878	blood:	n/a	chr1:104068541-104068550
12	BRCA1	chr1:104068257-104069233	Hela-S3	cervix:	n/a	chr1:104068541-104068550
13	CBX3	chr1:104068335-104068703	K562	blood:	n/a	n/a
14	CBX3	chr1:104068298-104068668	K562	blood:	n/a	n/a
15	CCNT2	chr1:104068442-104069153	K562	blood:	n/a	n/a
16	CEBPB	chr1:104067855-104068146	K562	blood:	n/a	n/a
17	CHD1	chr1:104068953-104069176	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD1	chr1:104068464-104069301	GM12878	blood:	n/a	chr1:104068541-104068550
19	CHD2	chr1:104068225-104069285	GM12878	blood:	n/a	chr1:104068541-104068550
20	CHD2	chr1:104067937-104068012	K562	blood:	n/a	n/a
21	CHD2	chr1:104068290-104068970	H1-hESC	embryonic stem cell:	n/a	chr1:104068541-104068550
22	CHD2	chr1:104067900-104069278	Hela-S3	cervix:	n/a	chr1:104068541-104068550
23	CHD2	chr1:104068272-104068999	HepG2	liver:	n/a	chr1:104068541-104068550
24	CHD2	chr1:104068248-104069181	K562	blood:	n/a	chr1:104068541-104068550
25	CREB1	chr1:104068282-104068752	A549	lung:	n/a	n/a
26	CREB1	chr1:104068364-104068701	A549	lung:	n/a	n/a
27	CTBP2	chr1:104068522-104069274	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr1:104068760-104068821	Fibrobl	skin:	n/a	n/a
29	CTCF	chr1:104068676-104068850	GM12891	blood:	n/a	n/a
30	CTCF	chr1:104068720-104068870	GM12871	blood:	n/a	n/a
31	CTCF	chr1:104068760-104068910	AG10803	skin:	n/a	n/a
32	CTCF	chr1:104068920-104069070	RPTEC	kidney:	n/a	n/a
33	CTCF	chr1:104068520-104068670	GM12873	blood:	n/a	n/a
34	CTCF	chr1:104068973-104069060	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr1:104068740-104068890	GM12864	blood:	n/a	n/a
36	CTCF	chr1:104068760-104068910	HPF	lung:	n/a	n/a
37	CTCF	chr1:104068680-104068830	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr1:104068820-104068970	AG09319	gingival:	n/a	n/a
39	CTCF	chr1:104068820-104068970	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr1:104068520-104068670	HRE	kidney:	n/a	n/a
41	CTCF	chr1:104068700-104068850	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr1:104068880-104069030	HRE	kidney:	n/a	n/a
43	CTCF	chr1:104068640-104068790	GM12872	blood:	n/a	n/a
44	CTCF	chr1:104068900-104069050	GM12874	blood:	n/a	n/a
45	CTCF	chr1:104068920-104069070	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr1:104068660-104068810	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr1:104068661-104068869	GM12892	blood:	n/a	n/a
48	CTCF	chr1:104068620-104068770	GM06990	blood:	n/a	n/a
49	CTCF	chr1:104068720-104068870	AG04449	skin:	n/a	n/a
50	CTCF	chr1:104068957-104069005	ProgFib	skin:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:104068301-104068351	HUVEC	blood vessel:	n/a
2	chr1:104068488-104068538	GM12891	blood:	n/a
3	chr1:104068704-104068754	HIPEpiC	eye:	n/a
4	chr1:104068567-104068617	H1-hESC	embryonic stem cell:	embryo
5	chr1:104068935-104068985	HUVEC	blood vessel:	n/a
6	chr1:104068704-104068754	HUVEC	blood vessel:	n/a
7	chr1:104068664-104068714	SK-N-SH	brain:	n/a
8	chr1:104068488-104068538	BJ	skin:	n/a
9	chr1:104068704-104068754	Jurkat	blood:	n/a
10	chr1:104068121-104068171	GM12878	blood:	n/a
11	chr1:104068121-104068171	NT2-D1	testis:	n/a
12	chr1:104068664-104068714	HIPEpiC	eye:	n/a
13	chr1:104068603-104068653	NHBE	bronchial:	n/a
14	chr1:104068567-104068617	GM12891	blood:	n/a
15	chr1:104068301-104068351	HMEC	breast:	n/a
16	chr1:104068490-104068540	PrEC	prostate:	n/a
17	chr1:104068121-104068171	HL-60	blood:	n/a
18	chr1:104068490-104068540	SK-N-SH	brain:	n/a
19	chr1:104068490-104068540	Jurkat	blood:	n/a
20	chr1:104068301-104068351	SK-N-SH	brain:	n/a
21	chr1:104068704-104068754	ProgFib	skin:	n/a
22	chr1:104068704-104068754	H1-hESC	embryonic stem cell:	embryo
23	chr1:104068118-104068168	SAEC	small airway:	n/a
24	chr1:104068603-104068653	HL-60	blood:	n/a
25	chr1:104068704-104068754	NH-A	brain:	n/a
26	chr1:104068488-104068538	U87	brain:	n/a
27	chr1:104068603-104068653	HEK293	kidney:	embryo
28	chr1:104068312-104068362	SAEC	small airway:	n/a
29	chr1:104068419-104068469	H1-hESC	embryonic stem cell:	embryo
30	chr1:104068121-104068171	T-47D	breast:	n/a
31	chr1:104068490-104068540	AoSMC	blood vessel:	n/a
32	chr1:104068419-104068469	T-47D	breast:	n/a
33	chr1:104068419-104068469	SAEC	small airway:	n/a
34	chr1:104068301-104068351	A549	lung:	n/a
35	chr1:104068935-104068985	HCF	heart:	n/a
36	chr1:104068603-104068653	SK-N-SH_RA	brain:	n/a
37	chr1:104068603-104068653	A549	lung:	n/a
38	chr1:104068490-104068540	BJ	skin:	n/a
39	chr1:104068312-104068362	NHBE	bronchial:	n/a
40	chr1:104068121-104068171	SK-N-SH_RA	brain:	n/a
41	chr1:104068488-104068538	ProgFib	skin:	n/a
42	chr1:104068419-104068469	HEK293	kidney:	embryo
43	chr1:104068118-104068168	H1-hESC	embryonic stem cell:	embryo
44	chr1:104068704-104068754	PrEC	prostate:	n/a
45	chr1:104068419-104068469	GM19239	blood:	n/a
46	chr1:104068301-104068351	NHDF-neo	bronchial:	n/a
47	chr1:104068301-104068351	Hela-S3	cervix:	n/a
48	chr1:104068488-104068538	ovcar-3	ovarian:	n/a
49	chr1:104068490-104068540	HMEC	breast:	n/a
50	chr1:104068419-104068469	BJ	skin:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:104068373..104071907-chr1:104081557..104086760,7	K562	blood:
2	chr1:104068563..104070409-chr1:104091369..104094625,4	MCF-7	breast:
3	chr1:104067956..104068800-chr18:9474823..9475445,2	Hela-S3	cervix:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMY1B-1	chr1:104068018-104068083	ENSG00000224613.2
2	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
3	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
4	lnc-AMY1B-1	chr1:104068018-104068115	XLOC_000945
5	lnc-AMY1B-1	chr1:104068018-104068105	XLOC_000945
6	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945

No data

Variant related genes	Relation type
ENSG00000224613	TF binding region
RNPC3	TF binding region
ENSG00000224613	CpG island
RNPC3	CpG island
ENSG00000185946	chromatin interactions
ENSG00000017797	chromatin interactions
TOMM34	miRNA target sites

Extended variants
information (count: 49 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:49 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28558115	chr1:104067608-104067609	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs538656276	chr1:104067722-104067723	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs200968943	chr1:104067737-104067738	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs368947863	chr1:104067738-104067739	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs202090325	chr1:104067739-104067740	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs201687120	chr1:104067750-104067751	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs542601987	chr1:104067758-104067759	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs533017819	chr1:104067767-104067768	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs536643962	chr1:104067789-104067790	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs116635881	chr1:104067864-104067865	Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs370747438	chr1:104067865-104067866	Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs76324549	chr1:104067877-104067878	Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs185133672	chr1:104067891-104067892	Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs571421240	chr1:104067917-104067918	Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs538502990	chr1:104067964-104067965	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs78290040	chr1:104068029-104068030	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs557008491	chr1:104068038-104068039	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs575278223	chr1:104068097-104068098	Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
19	rs542191804	chr1:104068276-104068277	Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs554163440	chr1:104068337-104068338	Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs368107151	chr1:104068379-104068380	Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs573163787	chr1:104068425-104068426	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs570077425	chr1:104068459-104068460	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs565291953	chr1:104068504-104068505	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs532738647	chr1:104068590-104068591	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs188456106	chr1:104068651-104068652	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs41299553	chr1:104068680-104068681	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs530164593	chr1:104068715-104068716	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs374597633	chr1:104068755-104068756	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs548979249	chr1:104068762-104068763	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs566889438	chr1:104068763-104068764	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs559208129	chr1:104068783-104068784	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs546911680	chr1:104068869-104068870	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs192837663	chr1:104068872-104068873	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs184721860	chr1:104068903-104068904	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs370688696	chr1:104068909-104068910	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs568903493	chr1:104068923-104068924	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs188871587	chr1:104068935-104068936	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs554102169	chr1:104068937-104068938	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs191349787	chr1:104068939-104068940	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs539890341	chr1:104068941-104068942	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs143297421	chr1:104068951-104068952	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs146220056	chr1:104068974-104068975	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs578116721	chr1:104068976-104068977	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs139161435	chr1:104068979-104068980	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs530184777	chr1:104068996-104068997	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs116692365	chr1:104069035-104069036	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs560614774	chr1:104069086-104069087	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs183922260	chr1:104069144-104069145	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
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
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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Cancer	22429812	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Multiple myeloma	17550852	CNVD
Schizophrenia	20967226	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	19287141	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:230 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:104065200-104067800	Enhancers	Fetal Intestine Large	intestine
2	chr1:104065800-104067800	Weak transcription	Fetal Stomach	stomach
3	chr1:104067200-104067800	Enhancers	Fetal Intestine Small	intestine
4	chr1:104067200-104067800	Enhancers	Placenta	Placenta
5	chr1:104067200-104071400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
6	chr1:104067400-104067800	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr1:104067400-104067800	Enhancers	Primary T cells fromperipheralblood	blood
8	chr1:104067400-104067800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr1:104067400-104067800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr1:104067400-104067800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr1:104067400-104067800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr1:104067400-104067800	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chr1:104067400-104067800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr1:104067400-104067800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr1:104067400-104067800	Enhancers	Colonic Mucosa	Colon
16	chr1:104067400-104067800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr1:104067400-104067800	Enhancers	Fetal Brain Male	brain
18	chr1:104067400-104067800	Enhancers	Pancreas	Pancrea
19	chr1:104067400-104067800	Flanking Active TSS	Psoas Muscle	Psoas
20	chr1:104067400-104067800	Enhancers	Sigmoid Colon	Sigmoid Colon
21	chr1:104067400-104067800	Flanking Active TSS	K562	blood
22	chr1:104067400-104068000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr1:104067400-104068000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr1:104067400-104068000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr1:104067400-104068000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
26	chr1:104067400-104068000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
27	chr1:104067400-104068000	Flanking Active TSS	Dnd41	blood
28	chr1:104067400-104068000	Flanking Active TSS	Hela-S3	cervix
29	chr1:104067400-104068000	Flanking Active TSS	HMEC	breast
30	chr1:104067400-104068000	Flanking Active TSS	NHEK	skin
31	chr1:104067400-104069400	Active TSS	HSMM	muscle
32	chr1:104067400-104069600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr1:104067400-104069600	Active TSS	Aorta	Aorta
34	chr1:104067400-104069600	Active TSS	Duodenum Smooth Muscle	Duodenum
35	chr1:104067400-104069800	Active TSS	Muscle Satellite Cultured Cells	--
36	chr1:104067400-104070000	Active TSS	A549	lung
37	chr1:104067400-104070600	Active TSS	Brain Inferior Temporal Lobe	brain
38	chr1:104067400-104070800	Active TSS	Right Ventricle	heart
39	chr1:104067400-104070800	Active TSS	Stomach Smooth Muscle	stomach
40	chr1:104067400-104071600	Active TSS	Right Atrium	heart
41	chr1:104067600-104067800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
42	chr1:104067600-104067800	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
43	chr1:104067600-104067800	Flanking Active TSS	Brain Angular Gyrus	brain
44	chr1:104067600-104067800	Enhancers	Fetal Thymus	thymus
45	chr1:104067600-104067800	Enhancers	Stomach Mucosa	stomach
46	chr1:104067600-104067800	Flanking Active TSS	NH-A	brain
47	chr1:104067600-104068000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr1:104067600-104068000	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr1:104067600-104068000	Flanking Active TSS	Primary B cells from cord blood	blood
50	chr1:104067600-104068000	Flanking Active TSS	Primary B cells from peripheral blood	blood

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