Variant report

Variant	esv3422811
Chromosome Location	chr7:150496544-150499392
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:14)
CpG islands
(count:1038)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:14 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:150498034-150498213	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:150497592-150497763	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:150497243-150497269	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD1	chr7:150498405-150498529	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr7:150497373-150497466	Kidney_OC	kidney:	n/a	chr7:150497384-150497392
6	E2F6	chr7:150498361-150499098	H1-hESC	embryonic stem cell:	n/a	n/a
7	HMGN3	chr7:150498743-150498807	K562	blood:	n/a	n/a
8	JUND	chr7:150498334-150498566	H1-hESC	embryonic stem cell:	n/a	n/a
9	MAX	chr7:150498733-150499082	H1-hESC	embryonic stem cell:	n/a	n/a
10	POLR2A	chr7:150498801-150498906	ProgFib	skin:	n/a	n/a
11	REST	chr7:150496901-150497108	H1-hESC	embryonic stem cell:	n/a	chr7:150496941-150496961 chr7:150496947-150496956
12	SUZ12	chr7:150497149-150497686	H1-hESC	embryonic stem cell:	n/a	n/a
13	SUZ12	chr7:150498235-150499076	H1-hESC	embryonic stem cell:	n/a	n/a
14	UBTF	chr7:150498962-150499018	K562	blood:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150497740-150497790	GM12892	blood:	n/a
2	chr7:150497740-150497790	GM12892	blood:	n/a
3	chr7:150498594-150498644	HepG2	liver:	n/a
4	chr7:150497669-150497719	RPTEC	kidney:	n/a
5	chr7:150497760-150497810	T-47D	breast:	n/a
6	chr7:150497346-150497396	Hepatocyte	liver:	n/a
7	chr7:150498493-150498543	NB4	blood:	n/a
8	chr7:150498493-150498543	MCF-7	breast:	n/a
9	chr7:150497760-150497810	NT2-D1	testis:	n/a
10	chr7:150497065-150497115	ProgFib	skin:	n/a
11	chr7:150498594-150498644	AoSMC	blood vessel:	n/a
12	chr7:150498843-150498893	Caco-2	colon:	n/a
13	chr7:150497065-150497115	HUVEC	blood vessel:	n/a
14	chr7:150497157-150497207	BJ	skin:	n/a
15	chr7:150498843-150498893	SKMC	muscle:	n/a
16	chr7:150497760-150497810	ECC-1	luminal epithelium:	n/a
17	chr7:150498594-150498644	HCF	heart:	n/a
18	chr7:150498843-150498893	SK-N-SH_RA	brain:	n/a
19	chr7:150498493-150498543	Jurkat	blood:	n/a
20	chr7:150497663-150497713	BJ	skin:	n/a
21	chr7:150497077-150497127	HRPEpiC	eye:	n/a
22	chr7:150498493-150498543	HPAEpiC	pulmonary alveolar:	n/a
23	chr7:150497496-150497546	AoSMC	blood vessel:	n/a
24	chr7:150498493-150498543	K562	blood:	n/a
25	chr7:150497346-150497396	SK-N-SH_RA	brain:	n/a
26	chr7:150499276-150499326	SK-N-SH	brain:	n/a
27	chr7:150497496-150497546	HAEpiC	amniotic membrane:	n/a
28	chr7:150497669-150497719	HCF	heart:	n/a
29	chr7:150497346-150497396	GM12878	blood:	n/a
30	chr7:150497738-150497788	HCF	heart:	n/a
31	chr7:150497760-150497810	SAEC	small airway:	n/a
32	chr7:150498594-150498644	BE2_C	brain:	n/a
33	chr7:150498594-150498644	HAEpiC	amniotic membrane:	n/a
34	chr7:150497157-150497207	LNCaP	prostate:	n/a
35	chr7:150498493-150498543	HCM	heart:	n/a
36	chr7:150497760-150497810	ProgFib	skin:	n/a
37	chr7:150497738-150497788	HEEpiC	esophagus:	n/a
38	chr7:150497065-150497115	AG10803	skin:	n/a
39	chr7:150497760-150497810	HNPCEpiC	eye:	n/a
40	chr7:150498594-150498644	SAEC	small airway:	n/a
41	chr7:150498843-150498893	AG04449	skin:	fetal
42	chr7:150498493-150498543	HNPCEpiC	eye:	n/a
43	chr7:150497663-150497713	ProgFib	skin:	n/a
44	chr7:150497663-150497713	NB4	blood:	n/a
45	chr7:150499276-150499326	RPTEC	kidney:	n/a
46	chr7:150499362-150499412	BE2_C	brain:	n/a
47	chr7:150498843-150498893	T-47D	breast:	n/a
48	chr7:150497663-150497713	RPTEC	kidney:	n/a
49	chr7:150497703-150497753	Jurkat	blood:	n/a
50	chr7:150498493-150498543	HEK293	kidney:	embryo

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:150490163..150495069-chr7:150496481..150500897,6	K562	blood:
2	chr7:150418208..150420407-chr7:150499249..150501046,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABP1-3	chr7:150499144-150500920	NONHSAT124157

No data

Variant related genes	Relation type
TMEM176B	TF binding region
TMEM176A	TF binding region
TMEM176B	CpG island
TMEM176A	CpG island
ENSG00000196329	chromatin interactions
ENSG00000106565	chromatin interactions

Extended variants
information (count: 101 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:101 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563468500	chr7:150496656-150496657	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs11972506	chr7:150496668-150496669	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
3	rs548835524	chr7:150496748-150496749	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs559136407	chr7:150496868-150496869	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs184733297	chr7:150496938-150496939	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs547579093	chr7:150496969-150496970	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs189492884	chr7:150497008-150497009	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs539490650	chr7:150497036-150497037	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs550135899	chr7:150497086-150497087	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs372494606	chr7:150497127-150497128	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs115827753	chr7:150497136-150497137	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs11769511	chr7:150497147-150497148	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs191379180	chr7:150497182-150497183	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs184529068	chr7:150497271-150497272	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs535214341	chr7:150497317-150497318	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs557606720	chr7:150497405-150497406	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs11546674	chr7:150497420-150497421	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs376684831	chr7:150497461-150497462	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs542735420	chr7:150497473-150497474	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs115946508	chr7:150497496-150497497	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs563316535	chr7:150497525-150497526	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs17173776	chr7:150497534-150497535	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs573266036	chr7:150497538-150497539	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs140839266	chr7:150497658-150497659	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs571569817	chr7:150497797-150497798	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs559175220	chr7:150497908-150497909	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs55775933	chr7:150497927-150497928	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs149708830	chr7:150497945-150497946	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs13650	chr7:150498045-150498046	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs533054013	chr7:150498063-150498064	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs374685705	chr7:150498164-150498165	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs189750707	chr7:150498194-150498195	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs533445739	chr7:150498216-150498217	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs114949263	chr7:150498245-150498246	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs570084213	chr7:150498253-150498254	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs145628171	chr7:150498295-150498296	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs549741435	chr7:150498310-150498311	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs566364954	chr7:150498329-150498330	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs534938676	chr7:150498358-150498359	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs555037666	chr7:150498360-150498361	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs1108577	chr7:150498419-150498420	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs72602541	chr7:150498448-150498449	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs5888418	chr7:150498449-150498450	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs79002088	chr7:150498450-150498451	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs537164898	chr7:150498487-150498488	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs114485788	chr7:150498491-150498492	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs555506707	chr7:150498503-150498504	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs1108578	chr7:150498508-150498509	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs11767388	chr7:150498520-150498521	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs552890419	chr7:150498546-150498547	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

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

Chromatin state (count:321 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150486600-150496600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr7:150489800-150496600	Weak transcription	Gastric	stomach
3	chr7:150489800-150496800	Weak transcription	Left Ventricle	heart
4	chr7:150490400-150496600	Weak transcription	Right Atrium	heart
5	chr7:150490400-150496600	Weak transcription	Right Ventricle	heart
6	chr7:150494600-150498800	Active TSS	Rectal Mucosa Donor 29	rectum
7	chr7:150495000-150498000	Active TSS	Duodenum Mucosa	Duodenum
8	chr7:150495000-150499200	Active TSS	Liver	Liver
9	chr7:150495800-150497600	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
10	chr7:150495800-150499400	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
11	chr7:150496000-150496600	Flanking Active TSS	Fetal Intestine Small	intestine
12	chr7:150496000-150498000	Bivalent/Poised TSS	Fetal Stomach	stomach
13	chr7:150496000-150498000	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
14	chr7:150496200-150496600	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr7:150496200-150496600	Bivalent Enhancer	Primary hematopoietic stem cells	blood
16	chr7:150496200-150496600	Flanking Active TSS	Fetal Intestine Large	intestine
17	chr7:150496200-150496600	Bivalent Enhancer	Fetal Muscle Leg	muscle
18	chr7:150496200-150496600	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 31	rectum
19	chr7:150496200-150496600	Active TSS	Small Intestine	intestine
20	chr7:150496200-150497000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr7:150496200-150497000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr7:150496200-150497200	Bivalent/Poised TSS	Adipose Nuclei	Adipose
23	chr7:150496200-150497200	Active TSS	Colonic Mucosa	Colon
24	chr7:150496200-150497400	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
25	chr7:150496200-150497600	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
26	chr7:150496200-150498800	Active TSS	Brain Anterior Caudate	brain
27	chr7:150496200-150499000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
28	chr7:150496200-150499600	Active TSS	Rectal Smooth Muscle	rectum
29	chr7:150496400-150496600	Bivalent Enhancer	Brain Cingulate Gyrus	brain
30	chr7:150496400-150496600	Flanking Bivalent TSS/Enh	Fetal Heart	heart
31	chr7:150496400-150496800	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
32	chr7:150496400-150496800	Flanking Active TSS	Ovary	ovary
33	chr7:150496400-150497000	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
34	chr7:150496400-150497000	Active TSS	Sigmoid Colon	Sigmoid Colon
35	chr7:150496400-150497400	Bivalent/Poised TSS	Brain Angular Gyrus	brain
36	chr7:150496400-150497400	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
37	chr7:150496400-150498800	Bivalent/Poised TSS	Brain Substantia Nigra	brain
38	chr7:150496400-150498800	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
39	chr7:150496400-150498800	Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr7:150496400-150499000	Bivalent/Poised TSS	Fetal Kidney	kidney
41	chr7:150496600-150496800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr7:150496600-150496800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
43	chr7:150496600-150496800	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
44	chr7:150496600-150496800	Bivalent/Poised TSS	Fetal Heart	heart
45	chr7:150496600-150496800	Active TSS	Fetal Intestine Large	intestine
46	chr7:150496600-150497000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr7:150496600-150497000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
48	chr7:150496600-150497000	Bivalent/Poised TSS	Esophagus	oesophagus
49	chr7:150496600-150497000	Enhancers	Lung	lung
50	chr7:150496600-150497000	Active TSS	Right Ventricle	heart

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