Variant report

Variant	nsv5881
Chromosome Location	chr7:102610488-102655699
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1112)
CpG islands
(count:244)
Chromatin interactive
region (count:44)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1112 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102615512-102615697	K562	blood:	n/a	n/a
2	ARID3A	chr7:102631977-102632469	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:102624128-102624420	K562	blood:	n/a	n/a
4	ARID3A	chr7:102628579-102628910	K562	blood:	n/a	n/a
5	ARID3A	chr7:102613385-102614106	K562	blood:	n/a	n/a
6	ARID3A	chr7:102622029-102622173	K562	blood:	n/a	n/a
7	ARID3A	chr7:102631471-102632633	K562	blood:	n/a	n/a
8	ARID3A	chr7:102618784-102618922	K562	blood:	n/a	n/a
9	ARID3A	chr7:102633170-102634240	K562	blood:	n/a	chr7:102633703-102633719
10	ARID3A	chr7:102623549-102623551	K562	blood:	n/a	n/a
11	ATF1	chr7:102632108-102632532	K562	blood:	n/a	n/a
12	ATF1	chr7:102615471-102615652	K562	blood:	n/a	n/a
13	ATF1	chr7:102613562-102614182	K562	blood:	n/a	n/a
14	ATF1	chr7:102618759-102618993	K562	blood:	n/a	n/a
15	ATF1	chr7:102633314-102633903	K562	blood:	n/a	n/a
16	ATF1	chr7:102624155-102624485	K562	blood:	n/a	n/a
17	ATF3	chr7:102631980-102632558	K562	blood:	n/a	n/a
18	ATF3	chr7:102631899-102632521	A549	lung:	n/a	n/a
19	ATF3	chr7:102613482-102614149	K562	blood:	n/a	n/a
20	ATF3	chr7:102632026-102632431	A549	lung:	n/a	n/a
21	ATF3	chr7:102632224-102632465	K562	blood:	n/a	n/a
22	ATF3	chr7:102633299-102634288	K562	blood:	n/a	n/a
23	BACH1	chr7:102633386-102633725	K562	blood:	n/a	n/a
24	BACH1	chr7:102613561-102613930	K562	blood:	n/a	n/a
25	BACH1	chr7:102613704-102613707	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr7:102632031-102632596	K562	blood:	n/a	chr7:102632279-102632293 chr7:102632306-102632320
27	BACH1	chr7:102619511-102619519	K562	blood:	n/a	n/a
28	BCLAF1	chr7:102613400-102614259	K562	blood:	n/a	n/a
29	BHLHE40	chr7:102622117-102622125	K562	blood:	n/a	n/a
30	BHLHE40	chr7:102631091-102631342	K562	blood:	n/a	n/a
31	BHLHE40	chr7:102633252-102633732	K562	blood:	n/a	n/a
32	BHLHE40	chr7:102622878-102622930	K562	blood:	n/a	n/a
33	BHLHE40	chr7:102613578-102614258	K562	blood:	n/a	n/a
34	BHLHE40	chr7:102615498-102615614	K562	blood:	n/a	n/a
35	BHLHE40	chr7:102624110-102624467	K562	blood:	n/a	n/a
36	BRCA1	chr7:102618851-102619385	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr7:102633359-102634284	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr7:102631647-102632684	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr7:102616016-102616744	K562	blood:	n/a	n/a
40	CBX3	chr7:102615174-102615822	K562	blood:	n/a	n/a
41	CBX3	chr7:102633296-102634159	K562	blood:	n/a	n/a
42	CBX3	chr7:102618539-102619152	K562	blood:	n/a	n/a
43	CBX3	chr7:102643449-102643794	HCT-116	colon:	n/a	n/a
44	CBX3	chr7:102643362-102643762	HCT-116	colon:	n/a	n/a
45	CBX3	chr7:102616799-102617613	K562	blood:	n/a	n/a
46	CBX3	chr7:102643394-102643836	K562	blood:	n/a	n/a
47	CBX3	chr7:102631953-102632801	K562	blood:	n/a	n/a
48	CBX3	chr7:102643432-102643742	K562	blood:	n/a	n/a
49	CBX3	chr7:102613423-102614555	K562	blood:	n/a	n/a
50	CBX3	chr7:102634847-102635567	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102614121-102614171	RPTEC	kidney:	n/a
2	chr7:102614121-102614171	PFSK-1	brain:	n/a
3	chr7:102614121-102614171	NT2-D1	testis:	n/a
4	chr7:102614121-102614171	MCF10A-Er-Src	breast:	n/a
5	chr7:102614121-102614171	NB4	blood:	n/a
6	chr7:102613596-102613646	NHDF-neo	bronchial:	n/a
7	chr7:102613596-102613646	HUVEC	blood vessel:	n/a
8	chr7:102613822-102613872	HPAEpiC	pulmonary alveolar:	n/a
9	chr7:102614121-102614171	SAEC	small airway:	n/a
10	chr7:102614121-102614171	T-47D	breast:	n/a
11	chr7:102614121-102614171	BJ	skin:	n/a
12	chr7:102614121-102614171	ECC-1	luminal epithelium:	n/a
13	chr7:102613822-102613872	HRCEpiC	kidney:	n/a
14	chr7:102632303-102632353	HRCEpiC	kidney:	n/a
15	chr7:102613596-102613646	HPAEpiC	pulmonary alveolar:	n/a
16	chr7:102614121-102614171	HPAEpiC	pulmonary alveolar:	n/a
17	chr7:102632303-102632353	AG09309	skin:	n/a
18	chr7:102632303-102632353	HRPEpiC	eye:	n/a
19	chr7:102613596-102613646	BJ	skin:	n/a
20	chr7:102613596-102613646	NB4	blood:	n/a
21	chr7:102613596-102613646	SK-N-MC	brain:	n/a
22	chr7:102632303-102632353	NB4	blood:	n/a
23	chr7:102614121-102614171	SK-N-SH	brain:	n/a
24	chr7:102632303-102632353	MCF-7	breast:	n/a
25	chr7:102632303-102632353	SKMC	muscle:	n/a
26	chr7:102613596-102613646	ECC-1	luminal epithelium:	n/a
27	chr7:102614121-102614171	AG09309	skin:	n/a
28	chr7:102613596-102613646	HEEpiC	esophagus:	n/a
29	chr7:102613596-102613646	Hela-S3	cervix:	n/a
30	chr7:102613822-102613872	Caco-2	colon:	n/a
31	chr7:102632303-102632353	HepG2	liver:	n/a
32	chr7:102614121-102614171	GM12891	blood:	n/a
33	chr7:102632303-102632353	ovcar-3	ovarian:	n/a
34	chr7:102613596-102613646	U87	brain:	n/a
35	chr7:102632303-102632353	IMR90	lung:	fetal
36	chr7:102614121-102614171	H1-hESC	embryonic stem cell:	embryo
37	chr7:102613596-102613646	Hepatocyte	liver:	n/a
38	chr7:102613822-102613872	HNPCEpiC	eye:	n/a
39	chr7:102614121-102614171	LNCaP	prostate:	n/a
40	chr7:102613596-102613646	H1-hESC	embryonic stem cell:	embryo
41	chr7:102613822-102613872	HRE	kidney:	n/a
42	chr7:102613596-102613646	PrEC	prostate:	n/a
43	chr7:102613822-102613872	HEEpiC	esophagus:	n/a
44	chr7:102613822-102613872	GM19239	blood:	n/a
45	chr7:102613596-102613646	HRE	kidney:	n/a
46	chr7:102614121-102614171	GM06990	blood:	n/a
47	chr7:102613822-102613872	NHDF-neo	bronchial:	n/a
48	chr7:102613822-102613872	A549	lung:	n/a
49	chr7:102613596-102613646	HIPEpiC	eye:	n/a
50	chr7:102632303-102632353	K562	blood:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:102537736..102539276-chr7:102622119..102624837,2	MCF-7	breast:
2	chr7:102629921..102632610-chr7:102634773..102637196,3	K562	blood:
3	chr7:102648277..102650266-chr7:102675319..102678268,2	K562	blood:
4	chr7:102573565..102575111-chr7:102627251..102629778,2	K562	blood:
5	chr7:102451931..102453738-chr7:102614138..102615717,2	K562	blood:
6	chr7:102608423..102610942-chr7:102700411..102702582,3	K562	blood:
7	chr7:102613006..102614516-chr7:102715583..102717366,2	K562	blood:
8	chr7:102618985..102623059-chr7:102696660..102699924,3	K562	blood:
9	chr7:102640940..102644654-chr7:102645333..102648344,5	K562	blood:
10	chr7:102635238..102638493-chr7:102639697..102643321,6	K562	blood:
11	chr7:102452440..102454909-chr7:102615064..102617723,2	K562	blood:
12	chr7:102644321..102646780-chr7:102650241..102652057,2	K562	blood:
13	chr7:102597576..102599200-chr7:102609739..102612061,2	K562	blood:
14	chr7:102635238..102638493-chr7:102639697..102643321,6	K562	blood:
15	chr7:102619656..102622103-chr7:102669784..102672550,2	K562	blood:
16	chr7:102616176..102618073-chr7:103034545..103036072,2	K562	blood:
17	chr7:102646044..102648834-chr7:102650144..102652467,2	MCF-7	breast:
18	chr7:102497060..102498758-chr7:102613043..102615053,2	K562	blood:
19	chr7:102640940..102642955-chr7:102645628..102648374,3	K562	blood:
20	chr7:102644321..102646780-chr7:102650241..102652057,2	K562	blood:
21	chr7:102635101..102637212-chr7:102643371..102644977,2	K562	blood:
22	chr7:102640940..102644654-chr7:102645333..102648344,5	K562	blood:
23	chr7:102616376..102618625-chr7:102696676..102699468,2	K562	blood:
24	chr7:102611388..102613212-chr7:102692044..102694457,2	K562	blood:
25	chr7:102628465..102631626-chr7:102631792..102634551,3	MCF-7	breast:
26	chr7:102627919..102629951-chr7:102630613..102632281,3	K562	blood:
27	chr7:102636271..102640995-chr7:102641350..102643321,4	K562	blood:
28	chr3:27525414..27526305-chr7:102633028..102633695,2	HCT-116	colon:
29	chr3:159480769..159481581-chr7:102631646..102632292,2	Hela-S3	cervix:
30	chr7:102620399..102622083-chr7:102705547..102707771,2	K562	blood:
31	chr7:102629638..102632111-chr7:102696219..102697817,2	K562	blood:
32	chr7:102636271..102640995-chr7:102641350..102643321,4	K562	blood:
33	chr7:102635365..102636884-chr7:102714071..102717009,2	K562	blood:
34	chr7:102628465..102631626-chr7:102631792..102634551,3	MCF-7	breast:
35	chr7:102586889..102588859-chr7:102610741..102612720,2	K562	blood:
36	chr7:102630195..102631725-chr7:102699498..102701582,2	K562	blood:
37	chr7:102646044..102648834-chr7:102650144..102652467,2	MCF-7	breast:
38	chr7:102629921..102632610-chr7:102634773..102637196,3	K562	blood:
39	chr7:102627919..102629951-chr7:102630613..102632281,3	K562	blood:
40	chr7:102632696..102634274-chr7:102635865..102637462,2	K562	blood:
41	chr7:102631511..102633980-chr7:102714406..102717077,3	K562	blood:
42	chr7:102635101..102637212-chr7:102643371..102644977,2	K562	blood:
43	chr7:102640940..102642955-chr7:102645628..102648374,3	K562	blood:
44	chr7:102632696..102634274-chr7:102635865..102637462,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC17-1	chr7:102618828-102618967	ENSG00000230257
2	lnc-LRRC17-1	chr7:102628480-102628679	ENSG00000230257
3	lnc-LRRC17-1	chr7:102628822-102629303	ENSG00000230257
4	lnc-LRRC17-1	chr7:102613969-102614218	ENSG00000230257

No data

Variant related genes	Relation type
FBXL13	TF binding region
ENSG00000264045	TF binding region
NFE4	TF binding region
FBXL13	CpG island
ENSG00000264045	CpG island
NFE4	CpG island
ENSG00000161040	chromatin interactions
ENSG00000236226	chromatin interactions
ENSG00000128606	chromatin interactions
ENSG00000238324	chromatin interactions
ENSG00000250588	chromatin interactions
ENSG00000170632	chromatin interactions
ENSG00000033867	chromatin interactions

Extended variants
information (count: 1513 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1513 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535527088	chr7:102610603-102610604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs569473527	chr7:102610687-102610688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs556741277	chr7:102610708-102610709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186776247	chr7:102610720-102610721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs545787484	chr7:102610728-102610729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114344784	chr7:102610738-102610739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs202075044	chr7:102610787-102610788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573158887	chr7:102610795-102610796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs2411060	chr7:102610796-102610797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs12671803	chr7:102610797-102610798	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs530174351	chr7:102610798-102610799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs183995378	chr7:102610807-102610808	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs566326894	chr7:102610813-102610814	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs73408272	chr7:102610842-102610843	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs552116441	chr7:102610903-102610904	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs149193255	chr7:102610906-102610907	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs553146529	chr7:102610938-102610939	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs78028208	chr7:102610944-102610945	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs186904261	chr7:102611002-102611003	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs560792554	chr7:102611055-102611056	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs191417812	chr7:102611085-102611086	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs146947273	chr7:102611086-102611087	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs375501624	chr7:102611146-102611147	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs535629222	chr7:102611236-102611237	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs182820989	chr7:102611259-102611260	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs187209547	chr7:102611275-102611276	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs58183016	chr7:102611282-102611283	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs573220320	chr7:102611320-102611321	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs540523471	chr7:102611379-102611380	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs561791456	chr7:102611421-102611422	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs192824686	chr7:102611424-102611425	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs558863035	chr7:102611443-102611444	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs116576850	chr7:102611462-102611463	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs563817127	chr7:102611508-102611509	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs530890447	chr7:102611523-102611524	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs545842550	chr7:102611531-102611532	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs564131395	chr7:102611602-102611603	Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs542181395	chr7:102611603-102611604	Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs138028994	chr7:102611663-102611664	Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs143390312	chr7:102611684-102611685	Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs185265476	chr7:102611685-102611686	Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs145798371	chr7:102611691-102611692	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs113579040	chr7:102611718-102611719	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs575509863	chr7:102611736-102611737	Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs550879557	chr7:102611759-102611760	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs138913156	chr7:102611813-102611814	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs563591520	chr7:102611823-102611824	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs141385907	chr7:102611838-102611839	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs34020421	chr7:102611859-102611860	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs566482465	chr7:102611868-102611869	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	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
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	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
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:350 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102591000-102619400	Weak transcription	HSMM	muscle
2	chr7:102607800-102611000	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr7:102608800-102618600	Weak transcription	Osteobl	bone
4	chr7:102609800-102613400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr7:102610000-102610800	Weak transcription	K562	blood
6	chr7:102610800-102611200	Flanking Active TSS	K562	blood
7	chr7:102611000-102611800	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr7:102611200-102611600	Active TSS	K562	blood
9	chr7:102611200-102612000	Enhancers	HUVEC	blood vessel
10	chr7:102611600-102611800	Transcr. at gene 5' and 3'	K562	blood
11	chr7:102611800-102612200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
12	chr7:102611800-102615000	Active TSS	K562	blood
13	chr7:102612000-102612400	Weak transcription	HUVEC	blood vessel
14	chr7:102612200-102613400	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr7:102612400-102612600	Enhancers	HUVEC	blood vessel
16	chr7:102612400-102613200	Active TSS	Primary hematopoietic stem cells	blood
17	chr7:102612400-102613600	Active TSS	Primary B cells from cord blood	blood
18	chr7:102612600-102613800	Flanking Active TSS	HUVEC	blood vessel
19	chr7:102613000-102625600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr7:102613200-102631200	Weak transcription	Primary hematopoietic stem cells	blood
21	chr7:102613400-102613600	Active TSS	Primary neutrophils fromperipheralblood	blood
22	chr7:102613400-102613800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr7:102613600-102614400	Enhancers	H1 Cell Line	embryonic stem cell
24	chr7:102613600-102615800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
25	chr7:102613800-102614000	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr7:102613800-102614200	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr7:102613800-102614200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr7:102613800-102614200	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr7:102613800-102615600	Enhancers	HUVEC	blood vessel
30	chr7:102613800-102617000	Weak transcription	Fetal Stomach	stomach
31	chr7:102613800-102618600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr7:102614200-102615200	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr7:102614200-102618600	Weak transcription	Primary monocytes fromperipheralblood	blood
34	chr7:102614200-102618800	Weak transcription	Monocytes-CD14+_RO01746	blood
35	chr7:102614400-102615200	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr7:102615000-102618000	Transcr. at gene 5' and 3'	K562	blood
37	chr7:102615200-102615400	Enhancers	H1 Cell Line	embryonic stem cell
38	chr7:102615200-102615600	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr7:102615600-102618600	Weak transcription	HUVEC	blood vessel
40	chr7:102615600-102619000	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr7:102615800-102616600	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr7:102616600-102617000	Active TSS	Primary neutrophils fromperipheralblood	blood
43	chr7:102616800-102617600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr7:102617000-102618000	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr7:102617600-102623600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr7:102618000-102620000	Genic enhancers	K562	blood
47	chr7:102618000-102620200	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr7:102618400-102630000	Weak transcription	Right Atrium	heart
49	chr7:102618600-102619200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr7:102618600-102619200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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