Variant report

Variant	esv1845627
Chromosome Location	chr7:97851109-97860507
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:96)
CpG islands
(count:489)
Chromatin interactive
region (count:16)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:96 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:97855510-97855782	HepG2	liver:	n/a	n/a
2	CCNT2	chr7:97857856-97857921	K562	blood:	n/a	n/a
3	CEBPB	chr7:97857481-97857783	IMR90	lung:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
4	CEBPB	chr7:97857468-97857755	K562	blood:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
5	CEBPB	chr7:97857458-97857785	A549	lung:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
6	CEBPB	chr7:97857410-97857839	MCF-7	breast:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
7	CEBPB	chr7:97857468-97857829	K562	blood:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
8	CEBPB	chr7:97857460-97857814	HepG2	liver:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
9	CEBPB	chr7:97857556-97857798	Hela-S3	cervix:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
10	CEBPB	chr7:97857541-97857759	H1-hESC	embryonic stem cell:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
11	CEBPB	chr7:97857558-97857722	K562	blood:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
12	CTCF	chr7:97859615-97859627	MCF-7	breast:	n/a	n/a
13	CTCF	chr7:97859562-97859687	K562	blood:	n/a	n/a
14	CTCF	chr7:97859476-97859741	K562	blood:	n/a	n/a
15	CTCF	chr7:97859505-97859705	GM12878	blood:	n/a	n/a
16	CTCF	chr7:97859564-97859690	GM19238	blood:	n/a	n/a
17	CTCF	chr7:97859540-97859690	WERI-Rb-1	eye:	n/a	n/a
18	CTCF	chr7:97859586-97859663	MCF-7	breast:	n/a	n/a
19	CTCF	chr7:97859500-97859650	GM12873	blood:	n/a	n/a
20	CTCF	chr7:97854030-97854041	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr7:97859600-97859750	GM12864	blood:	n/a	n/a
22	CTCF	chr7:97859554-97859689	GM12891	blood:	n/a	n/a
23	CTCF	chr7:97859612-97859668	GM19240	blood:	n/a	n/a
24	CTCF	chr7:97859566-97859694	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr7:97859611-97859660	K562	blood:	n/a	n/a
26	CTCF	chr7:97859560-97859710	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr7:97859593-97859672	MCF-7	breast:	n/a	n/a
28	CTCF	chr7:97859600-97859750	HepG2	liver:	n/a	n/a
29	CTCF	chr7:97859483-97859700	K562	blood:	n/a	n/a
30	CTCF	chr7:97859598-97859710	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr7:97859579-97859690	GM12878	blood:	n/a	n/a
32	CTCF	chr7:97859540-97859690	GM12871	blood:	n/a	n/a
33	CTCF	chr7:97858895-97858946	GM20000	blood:	n/a	n/a
34	CTCF	chr7:97859531-97859712	HepG2	liver:	n/a	n/a
35	CTCF	chr7:97859588-97859689	MCF-7	breast:	n/a	n/a
36	CTCF	chr7:97859560-97859710	A549	lung:	n/a	n/a
37	CTCF	chr7:97859540-97859690	GM12873	blood:	n/a	n/a
38	CTCF	chr7:97859633-97859670	GM19239	blood:	n/a	n/a
39	CTCF	chr7:97859540-97859690	GM12868	blood:	n/a	n/a
40	CTCF	chr7:97859547-97859690	GM12892	blood:	n/a	n/a
41	CTCF	chr7:97859595-97859662	HepG2	liver:	n/a	n/a
42	CTCF	chr7:97859560-97859710	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr7:97859559-97859657	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr7:97859520-97859670	GM12873	blood:	n/a	n/a
45	CTCF	chr7:97853955-97854015	H1-hESC	embryonic stem cell:	n/a	chr7:97853977-97853986
46	CTCF	chr7:97859560-97859710	GM12870	blood:	n/a	n/a
47	CTCFL	chr7:97859554-97859652	K562	blood:	n/a	n/a
48	FOXA1	chr7:97855433-97855816	HepG2	liver:	n/a	n/a
49	FOXA1	chr7:97852988-97853225	T-47D	breast:	n/a	n/a
50	FOXA1	chr7:97855385-97855831	HepG2	liver:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:97857971-97858021	HRCEpiC	kidney:	n/a
2	chr7:97857971-97858021	HRCEpiC	kidney:	n/a
3	chr7:97857647-97857697	GM12892	blood:	n/a
4	chr7:97857492-97857542	HRE	kidney:	n/a
5	chr7:97857989-97858039	A549	lung:	n/a
6	chr7:97857938-97857988	NH-A	brain:	n/a
7	chr7:97857971-97858021	NB4	blood:	n/a
8	chr7:97857971-97858021	PANC-1	pancreas:	n/a
9	chr7:97857492-97857542	HNPCEpiC	eye:	n/a
10	chr7:97851854-97851904	SKMC	muscle:	n/a
11	chr7:97851854-97851904	MCF-7	breast:	n/a
12	chr7:97857938-97857988	PrEC	prostate:	n/a
13	chr7:97857938-97857988	HepG2	liver:	n/a
14	chr7:97852022-97852072	HMEC	breast:	n/a
15	chr7:97852022-97852072	HPAEpiC	pulmonary alveolar:	n/a
16	chr7:97857492-97857542	HRPEpiC	eye:	n/a
17	chr7:97857938-97857988	SAEC	small airway:	n/a
18	chr7:97852022-97852072	ovcar-3	ovarian:	n/a
19	chr7:97857938-97857988	Hela-S3	cervix:	n/a
20	chr7:97857356-97857406	GM12891	blood:	n/a
21	chr7:97857938-97857988	Hepatocyte	liver:	n/a
22	chr7:97857938-97857988	A549	lung:	n/a
23	chr7:97857971-97858021	T-47D	breast:	n/a
24	chr7:97857356-97857406	HEEpiC	esophagus:	n/a
25	chr7:97852022-97852072	CMK	blood:	n/a
26	chr7:97857647-97857697	NB4	blood:	n/a
27	chr7:97851854-97851904	HL-60	blood:	n/a
28	chr7:97857492-97857542	SKMC	muscle:	n/a
29	chr7:97857647-97857697	AG10803	skin:	n/a
30	chr7:97857647-97857697	NHDF-neo	bronchial:	n/a
31	chr7:97857356-97857406	HCT-116	colon:	n/a
32	chr7:97852022-97852072	GM12878	blood:	n/a
33	chr7:97852022-97852072	GM19239	blood:	n/a
34	chr7:97857356-97857406	SAEC	small airway:	n/a
35	chr7:97857989-97858039	PANC-1	pancreas:	n/a
36	chr7:97857647-97857697	HEEpiC	esophagus:	n/a
37	chr7:97857971-97858021	SK-N-MC	brain:	n/a
38	chr7:97857938-97857988	SKMC	muscle:	n/a
39	chr7:97857938-97857988	RPTEC	kidney:	n/a
40	chr7:97852022-97852072	AG09319	gingival:	n/a
41	chr7:97857356-97857406	SKMC	muscle:	n/a
42	chr7:97857938-97857988	HEEpiC	esophagus:	n/a
43	chr7:97857492-97857542	GM12892	blood:	n/a
44	chr7:97857938-97857988	HRE	kidney:	n/a
45	chr7:97852022-97852072	NHDF-neo	bronchial:	n/a
46	chr7:97857356-97857406	HCPEpiC	choroid plexus:	n/a
47	chr7:97857492-97857542	SAEC	small airway:	n/a
48	chr7:97857971-97858021	AG04450	lung:	fetal
49	chr7:97857492-97857542	HepG2	liver:	n/a
50	chr7:97851854-97851904	GM12892	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:97841230..97842751-chr7:97851743..97853660,2	K562	blood:
2	chr7:97852333..97858295-chr7:97859641..97865309,7	MCF-7	breast:
3	chr7:97736018..97736542-chr7:97859141..97859647,2	K562	blood:
4	chr7:97855900..97859430-chr7:97859536..97863597,5	K562	blood:
5	chr7:97843013..97845825-chr7:97853837..97855430,2	MCF-7	breast:
6	chr7:97849669..97852515-chr7:97854128..97855997,2	MCF-7	breast:
7	chr7:97850503..97852580-chr7:97856044..97857561,2	MCF-7	breast:
8	chr7:97845652..97847962-chr7:97851352..97854034,2	MCF-7	breast:
9	chr7:97840601..97843525-chr7:97854047..97856792,2	MCF-7	breast:
10	chr7:97854372..97856436-chr7:97905266..97907266,2	MCF-7	breast:
11	chr7:97851992..97854043-chr7:98027877..98030619,2	K562	blood:
12	chr7:97852038..97854221-chr7:97858720..97861626,2	K562	blood:
13	chr7:97852038..97854221-chr7:97858720..97861626,2	K562	blood:
14	chr7:97855900..97859430-chr7:97859536..97863597,5	K562	blood:
15	chr7:97846624..97850033-chr7:97850682..97852457,3	MCF-7	breast:
16	chr7:97852333..97858295-chr7:97859641..97865309,7	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BAIAP2L1.1-1	chr7:97855904-97856081	NONHSAT122183

No data

Variant related genes	Relation type
TECPR1	TF binding region
TECPR1	CpG island
ENSG00000164715	chromatin interactions
ENSG00000180535	chromatin interactions
ENSG00000205356	chromatin interactions
ENSG00000006453	chromatin interactions

Extended variants
information (count: 440 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:440 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4729416	chr7:97851109-97851110	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs527873459	chr7:97851191-97851192	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs575568728	chr7:97851251-97851252	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs58265945	chr7:97851252-97851253	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs372330104	chr7:97851278-97851279	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs371378969	chr7:97851372-97851373	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs564590862	chr7:97851496-97851497	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs528638123	chr7:97851503-97851504	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs540826607	chr7:97851541-97851542	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs375388965	chr7:97851549-97851550	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs562216147	chr7:97851551-97851552	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs34385473	chr7:97851594-97851595	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs576824184	chr7:97851619-97851620	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs551221055	chr7:97851656-97851657	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs369834776	chr7:97851686-97851687	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs569470700	chr7:97851694-97851695	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs530502380	chr7:97851715-97851716	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs113469464	chr7:97851720-97851721	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs570515591	chr7:97851728-97851729	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs534455397	chr7:97851738-97851739	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs376799220	chr7:97851755-97851756	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs369865845	chr7:97851780-97851781	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs570872157	chr7:97851789-97851790	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs546302230	chr7:97851794-97851795	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs373441649	chr7:97851815-97851816	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs567882496	chr7:97851847-97851848	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs535291214	chr7:97851891-97851892	Strong transcription Weak transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs368053881	chr7:97851923-97851924	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs557201127	chr7:97851972-97851973	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs375924002	chr7:97851983-97851984	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs58063358	chr7:97851987-97851988	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs76067965	chr7:97852006-97852007	Strong transcription Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs539813017	chr7:97852023-97852024	Strong transcription Weak transcription Enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs557913387	chr7:97852036-97852037	Strong transcription Weak transcription Enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs573277629	chr7:97852047-97852048	Strong transcription Weak transcription Enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs74786155	chr7:97852048-97852049	Strong transcription Weak transcription Enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs374728600	chr7:97852062-97852063	Strong transcription Weak transcription Enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs562179058	chr7:97852066-97852067	Strong transcription Weak transcription Enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs531790061	chr7:97852098-97852099	Strong transcription Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs544506589	chr7:97852099-97852100	Strong transcription Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs563179614	chr7:97852103-97852104	Strong transcription Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs371930160	chr7:97852246-97852247	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs184028270	chr7:97852256-97852257	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs368677869	chr7:97852279-97852280	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs10231290	chr7:97852281-97852282	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs549909468	chr7:97852314-97852315	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs79438349	chr7:97852317-97852318	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs376386211	chr7:97852322-97852323	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs200796145	chr7:97852323-97852324	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs374207921	chr7:97852324-97852325	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myoclonus-dystonia	17898012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164920	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Chronic myeloid leukemia	21384125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:339 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97836800-97857200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr7:97840400-97852800	Weak transcription	Brain Angular Gyrus	brain
3	chr7:97841000-97858600	Weak transcription	Psoas Muscle	Psoas
4	chr7:97841200-97852200	Weak transcription	A549	lung
5	chr7:97841200-97867800	Weak transcription	HUVEC	blood vessel
6	chr7:97841200-97880200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr7:97841400-97858600	Weak transcription	NH-A	brain
8	chr7:97841400-97866200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr7:97841400-97879400	Weak transcription	Fetal Brain Male	brain
10	chr7:97841400-97880200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr7:97841600-97853800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr7:97841800-97867400	Weak transcription	Rectal Smooth Muscle	rectum
13	chr7:97842200-97868400	Weak transcription	Colon Smooth Muscle	Colon
14	chr7:97843400-97855000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr7:97843800-97857000	Weak transcription	Right Atrium	heart
16	chr7:97845200-97877400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr7:97846800-97856400	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr7:97847000-97851200	Weak transcription	Small Intestine	intestine
19	chr7:97848000-97852800	Weak transcription	HepG2	liver
20	chr7:97848000-97857600	Weak transcription	Stomach Mucosa	stomach
21	chr7:97848000-97877600	Weak transcription	Primary hematopoietic stem cells	blood
22	chr7:97848000-97880600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr7:97848600-97873200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr7:97848800-97855200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr7:97849000-97864600	Strong transcription	Primary T helper cells fromperipheralblood	blood
26	chr7:97849200-97857800	Strong transcription	Fetal Muscle Leg	muscle
27	chr7:97849400-97863400	Strong transcription	Primary T helper cells PMA-I stimulated	--
28	chr7:97849800-97858000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr7:97850000-97871800	Strong transcription	Primary neutrophils fromperipheralblood	blood
30	chr7:97850000-97878000	Strong transcription	Fetal Stomach	stomach
31	chr7:97850200-97851800	Strong transcription	Primary T cells from cord blood	blood
32	chr7:97850200-97858200	Strong transcription	Liver	Liver
33	chr7:97850200-97874400	Strong transcription	Monocytes-CD14+_RO01746	blood
34	chr7:97850200-97875400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr7:97850400-97872800	Strong transcription	Primary T cells fromperipheralblood	blood
36	chr7:97850400-97878600	Weak transcription	GM12878-XiMat	blood
37	chr7:97850600-97851200	Genic enhancers	Primary B cells from peripheral blood	blood
38	chr7:97850600-97851600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr7:97850600-97851800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr7:97850600-97851800	Strong transcription	Muscle Satellite Cultured Cells	--
41	chr7:97850600-97851800	Strong transcription	Duodenum Smooth Muscle	Duodenum
42	chr7:97850600-97852200	Strong transcription	Primary T helper naive cells from peripheral blood	blood
43	chr7:97850600-97852200	Strong transcription	Cortex derived primary cultured neurospheres	brain
44	chr7:97850600-97852600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr7:97850600-97853200	Strong transcription	Stomach Smooth Muscle	stomach
46	chr7:97850600-97855400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr7:97850600-97855600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr7:97850600-97856200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr7:97850600-97856200	Strong transcription	Brain Germinal Matrix	brain
50	chr7:97850600-97864200	Strong transcription	Primary monocytes fromperipheralblood	blood

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