Variant report

Variant	esv3389454
Chromosome Location	chr7:150748469-150750967
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:112)
CpG islands
(count:122)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:112 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr7:150748195-150748506	GM12878	blood:	n/a	n/a
2	BHLHE40	chr7:150750134-150750183	K562	blood:	n/a	n/a
3	BHLHE40	chr7:150748136-150748501	HepG2	liver:	n/a	n/a
4	BRCA1	chr7:150748277-150748480	H1-hESC	embryonic stem cell:	n/a	n/a
5	CCNT2	chr7:150748316-150748487	K562	blood:	n/a	n/a
6	CEBPB	chr7:150748176-150748676	IMR90	lung:	n/a	n/a
7	CEBPB	chr7:150748171-150748609	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD1	chr7:150748020-150748657	IMR90	lung:	n/a	n/a
9	CHD2	chr7:150748131-150748541	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr7:150750156-150750373	K562	blood:	n/a	n/a
11	CREB1	chr7:150747965-150748603	H1-hESC	embryonic stem cell:	n/a	n/a
12	E2F6	chr7:150748010-150748603	H1-hESC	embryonic stem cell:	n/a	chr7:150748216-150748225
13	E2F6	chr7:150747835-150748619	H1-hESC	embryonic stem cell:	n/a	chr7:150748216-150748225
14	ELF1	chr7:150750169-150750569	K562	blood:	n/a	n/a
15	ELF1	chr7:150748090-150748573	GM12878	blood:	n/a	chr7:150748212-150748224
16	ELF1	chr7:150748172-150748495	K562	blood:	n/a	chr7:150748212-150748224
17	GABPA	chr7:150747986-150748565	H1-hESC	embryonic stem cell:	n/a	chr7:150748219-150748228 chr7:150748068-150748077
18	GABPA	chr7:150748058-150748591	H1-hESC	embryonic stem cell:	n/a	chr7:150748219-150748228 chr7:150748068-150748077
19	GTF2F1	chr7:150748277-150748477	H1-hESC	embryonic stem cell:	n/a	n/a
20	HMGN3	chr7:150748134-150748556	K562	blood:	n/a	n/a
21	JUND	chr7:150748245-150748473	H1-hESC	embryonic stem cell:	n/a	chr7:150748416-150748425 chr7:150748420-150748429
22	MAFF	chr7:150750010-150750175	K562	blood:	n/a	n/a
23	MAFK	chr7:150749991-150750170	HepG2	liver:	n/a	chr7:150750118-150750132 chr7:150750115-150750130 chr7:150750115-150750131 chr7:150750119-150750130 chr7:150750120-150750131 chr7:150750120-150750131
24	MAFK	chr7:150750005-150750182	HepG2	liver:	n/a	chr7:150750118-150750132 chr7:150750115-150750130 chr7:150750115-150750131 chr7:150750119-150750130 chr7:150750120-150750131 chr7:150750120-150750131
25	MAX	chr7:150748109-150748505	H1-hESC	embryonic stem cell:	n/a	n/a
26	MAX	chr7:150747933-150748569	H1-hESC	embryonic stem cell:	n/a	n/a
27	MAX	chr7:150747970-150748589	ECC-1	luminal epithelium:	n/a	n/a
28	MAX	chr7:150748123-150748556	HepG2	liver:	n/a	n/a
29	MAX	chr7:150748125-150748560	NB4	blood:	n/a	n/a
30	MAX	chr7:150747977-150748599	ECC-1	luminal epithelium:	n/a	n/a
31	MAX	chr7:150747885-150748585	H1-hESC	embryonic stem cell:	n/a	n/a
32	MAX	chr7:150748110-150748515	HUVEC	blood vessel:	n/a	n/a
33	MAZ	chr7:150750224-150750444	K562	blood:	n/a	n/a
34	MAZ	chr7:150748053-150748775	IMR90	lung:	n/a	n/a
35	MXI1	chr7:150747336-150748663	IMR90	lung:	n/a	n/a
36	MXI1	chr7:150748100-150748517	H1-hESC	embryonic stem cell:	n/a	n/a
37	MYC	chr7:150748132-150748542	NB4	blood:	n/a	n/a
38	MYC	chr7:150748148-150748470	MCF10A-Er-Src	breast:	n/a	n/a
39	MYC	chr7:150748112-150748523	H1-hESC	embryonic stem cell:	n/a	n/a
40	NFIC	chr7:150748052-150748557	ECC-1	luminal epithelium:	n/a	n/a
41	NRF1	chr7:150748255-150748477	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr7:150748313-150748866	K562	blood:	n/a	n/a
43	POLR2A	chr7:150750616-150750619	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr7:150748709-150748771	ProgFib	skin:	n/a	n/a
45	POLR2A	chr7:150750386-150750588	K562	blood:	n/a	n/a
46	POLR2A	chr7:150748100-150748631	H1-neurons	neurons:	n/a	n/a
47	POLR2A	chr7:150749085-150749102	K562	blood:	n/a	n/a
48	POLR2A	chr7:150749163-150749881	K562	blood:	n/a	n/a
49	POLR2A	chr7:150749897-150749905	K562	blood:	n/a	n/a
50	POLR2A	chr7:150748036-150748473	HUVEC	blood vessel:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150748518-150748568	PrEC	prostate:	n/a
2	chr7:150749758-150749808	AG10803	skin:	n/a
3	chr7:150748518-150748568	AG04450	lung:	fetal
4	chr7:150749758-150749808	AoSMC	blood vessel:	n/a
5	chr7:150749758-150749808	HRPEpiC	eye:	n/a
6	chr7:150748518-150748568	SK-N-SH_RA	brain:	n/a
7	chr7:150749758-150749808	BJ	skin:	n/a
8	chr7:150749758-150749808	LNCaP	prostate:	n/a
9	chr7:150748518-150748568	Hela-S3	cervix:	n/a
10	chr7:150749758-150749808	HCPEpiC	choroid plexus:	n/a
11	chr7:150749758-150749808	GM06990	blood:	n/a
12	chr7:150748518-150748568	BJ	skin:	n/a
13	chr7:150749758-150749808	GM12892	blood:	n/a
14	chr7:150748518-150748568	HPAEpiC	pulmonary alveolar:	n/a
15	chr7:150749758-150749808	Hela-S3	cervix:	n/a
16	chr7:150748518-150748568	AG04449	skin:	fetal
17	chr7:150748518-150748568	CMK	blood:	n/a
18	chr7:150749758-150749808	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:150748518-150748568	LNCaP	prostate:	n/a
20	chr7:150749758-150749808	HRCEpiC	kidney:	n/a
21	chr7:150749758-150749808	GM12878	blood:	n/a
22	chr7:150748518-150748568	HEEpiC	esophagus:	n/a
23	chr7:150748518-150748568	SK-N-SH	brain:	n/a
24	chr7:150749758-150749808	A549	lung:	n/a
25	chr7:150748518-150748568	HCT-116	colon:	n/a
26	chr7:150749758-150749808	GM12891	blood:	n/a
27	chr7:150749758-150749808	HMEC	breast:	n/a
28	chr7:150749758-150749808	ovcar-3	ovarian:	n/a
29	chr7:150748518-150748568	HMEC	breast:	n/a
30	chr7:150748518-150748568	U87	brain:	n/a
31	chr7:150748518-150748568	IMR90	lung:	fetal
32	chr7:150749758-150749808	NB4	blood:	n/a
33	chr7:150748518-150748568	ProgFib	skin:	n/a
34	chr7:150749758-150749808	NHBE	bronchial:	n/a
35	chr7:150749758-150749808	HepG2	liver:	n/a
36	chr7:150749758-150749808	HCF	heart:	n/a
37	chr7:150749758-150749808	HUVEC	blood vessel:	n/a
38	chr7:150749758-150749808	HEK293	kidney:	embryo
39	chr7:150748518-150748568	GM06990	blood:	n/a
40	chr7:150749758-150749808	IMR90	lung:	fetal
41	chr7:150749758-150749808	SK-N-MC	brain:	n/a
42	chr7:150748518-150748568	HAEpiC	amniotic membrane:	n/a
43	chr7:150749758-150749808	H1-hESC	embryonic stem cell:	embryo
44	chr7:150749758-150749808	GM19239	blood:	n/a
45	chr7:150748518-150748568	Caco-2	colon:	n/a
46	chr7:150748518-150748568	K562	blood:	n/a
47	chr7:150749758-150749808	Hepatocyte	liver:	n/a
48	chr7:150748518-150748568	HUVEC	blood vessel:	n/a
49	chr7:150748518-150748568	HRE	kidney:	n/a
50	chr7:150749758-150749808	MCF10A-Er-Src	breast:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:150064606..150067565-chr7:150746513..150748694,2	MCF-7	breast:

No data

Variant related genes	Relation type
SLC4A2	TF binding region
SLC4A2	CpG island
ENSG00000214022	chromatin interactions
ENSG00000196456	chromatin interactions

Extended variants
information (count: 120 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:120 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540130534	chr7:150748470-150748471	Bivalent/Poised TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs556245886	chr7:150748540-150748541	Bivalent/Poised TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs541056759	chr7:150748597-150748598	Bivalent/Poised TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs535528995	chr7:150748604-150748605	Bivalent Enhancer Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs555421912	chr7:150748656-150748657	Bivalent Enhancer Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs572220303	chr7:150748661-150748662	Bivalent Enhancer Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs540797382	chr7:150748680-150748681	Bivalent Enhancer Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs369106138	chr7:150748708-150748709	Bivalent Enhancer Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs559604506	chr7:150748725-150748726	Bivalent Enhancer Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs557531105	chr7:150748731-150748732	Bivalent Enhancer Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577819142	chr7:150748761-150748762	Bivalent Enhancer Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs58134191	chr7:150748771-150748772	Bivalent Enhancer Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs371256322	chr7:150748858-150748859	Bivalent Enhancer ZNF genes & repeats Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs200114588	chr7:150748859-150748860	Bivalent Enhancer ZNF genes & repeats Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs10255526	chr7:150748869-150748870	Bivalent Enhancer ZNF genes & repeats Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs202074862	chr7:150748892-150748893	Bivalent Enhancer ZNF genes & repeats Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs559456655	chr7:150748943-150748944	Bivalent Enhancer ZNF genes & repeats Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs150496362	chr7:150748949-150748950	Bivalent Enhancer ZNF genes & repeats Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs374603867	chr7:150748956-150748957	Bivalent Enhancer ZNF genes & repeats Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs115179904	chr7:150748960-150748961	Bivalent Enhancer ZNF genes & repeats Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs547966092	chr7:150748968-150748969	Bivalent Enhancer ZNF genes & repeats Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs371968452	chr7:150749007-150749008	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs375324927	chr7:150749012-150749013	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541273309	chr7:150749013-150749014	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs201230822	chr7:150749019-150749020	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs368220067	chr7:150749022-150749023	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs200298732	chr7:150749025-150749026	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs201843515	chr7:150749031-150749032	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs372505837	chr7:150749056-150749057	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs151249670	chr7:150749062-150749063	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535804340	chr7:150749071-150749072	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs199642384	chr7:150749076-150749077	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565809530	chr7:150749086-150749087	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs201063435	chr7:150749125-150749126	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs200524358	chr7:150749126-150749127	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs557865888	chr7:150749175-150749176	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs370096272	chr7:150749187-150749188	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs373184803	chr7:150749195-150749196	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75042382	chr7:150749199-150749200	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs6978641	chr7:150749211-150749212	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs373281304	chr7:150749230-150749231	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs192889290	chr7:150749234-150749235	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs370705676	chr7:150749259-150749260	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs114216747	chr7:150749260-150749261	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs145339468	chr7:150749289-150749290	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs373214644	chr7:150749334-150749335	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs376432727	chr7:150749348-150749349	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs528157488	chr7:150749374-150749375	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs545107973	chr7:150749380-150749381	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs564855436	chr7:150749393-150749394	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150736800-150753800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:150738600-150749600	Weak transcription	K562	blood
3	chr7:150739600-150750000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr7:150740200-150753800	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr7:150741400-150749400	Weak transcription	Brain Substantia Nigra	brain
6	chr7:150741600-150751200	Weak transcription	Primary B cells from cord blood	blood
7	chr7:150742600-150754400	Weak transcription	Aorta	Aorta
8	chr7:150742800-150750200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr7:150743200-150748800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr7:150743800-150749200	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr7:150743800-150753800	Weak transcription	Liver	Liver
12	chr7:150744000-150748800	Weak transcription	Primary T cells from cord blood	blood
13	chr7:150744200-150748800	Weak transcription	Brain Angular Gyrus	brain
14	chr7:150744400-150751200	Weak transcription	Brain Cingulate Gyrus	brain
15	chr7:150744400-150754000	Weak transcription	A549	lung
16	chr7:150744800-150754200	Weak transcription	Right Atrium	heart
17	chr7:150745200-150754000	Weak transcription	HSMMtube	muscle
18	chr7:150745200-150754200	Weak transcription	NHDF-Ad	bronchial
19	chr7:150746000-150754000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr7:150746600-150749200	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr7:150747200-150749600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
22	chr7:150747800-150748600	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr7:150747800-150748600	Enhancers	Primary T helper naive cells from peripheral blood	blood
24	chr7:150747800-150748600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
25	chr7:150747800-150748600	Bivalent/Poised TSS	Fetal Brain Female	brain
26	chr7:150747800-150748600	Enhancers	Lung	lung
27	chr7:150747800-150749000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr7:150747800-150749000	Bivalent Enhancer	Fetal Muscle Leg	muscle
29	chr7:150747800-150749200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr7:150747800-150749200	Bivalent Enhancer	Fetal Thymus	thymus
31	chr7:150747800-150749400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
32	chr7:150748000-150748600	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
33	chr7:150748000-150748600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr7:150748000-150748600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
35	chr7:150748000-150748600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr7:150748000-150748600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
37	chr7:150748000-150748600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
38	chr7:150748000-150748600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
39	chr7:150748000-150748600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr7:150748000-150748600	Enhancers	Primary T helper cells fromperipheralblood	blood
41	chr7:150748000-150748600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr7:150748000-150748600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr7:150748000-150748600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr7:150748000-150748600	Bivalent Enhancer	Fetal Stomach	stomach
45	chr7:150748000-150748600	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr7:150748000-150748600	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr7:150748000-150748600	Flanking Active TSS	Dnd41	blood
48	chr7:150748000-150748600	Active TSS	NHEK	skin
49	chr7:150748000-150748800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
50	chr7:150748000-150749000	Enhancers	Cortex derived primary cultured neurospheres	brain

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