Variant report

Variant	nsv482758
Chromosome Location	chr7:101231458-101395219
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2743)
CpG islands
(count:1831)
Chromatin interactive
region (count:203)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2743 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:101372583-101373061	K562	blood:	n/a	n/a
2	ARID3A	chr7:101386542-101387010	K562	blood:	n/a	n/a
3	ARID3A	chr7:101386678-101386965	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:101245724-101245971	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:101337005-101337230	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:101331702-101331804	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:101377188-101377388	K562	blood:	n/a	n/a
8	ARID3A	chr7:101361030-101361265	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:101345677-101345966	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:101372660-101372980	HepG2	liver:	n/a	n/a
11	ATF1	chr7:101238094-101238243	K562	blood:	n/a	n/a
12	ATF1	chr7:101372567-101373075	K562	blood:	n/a	n/a
13	ATF2	chr7:101384128-101384640	GM12878	blood:	n/a	n/a
14	ATF3	chr7:101331375-101331865	K562	blood:	n/a	chr7:101331769-101331789
15	ATF3	chr7:101331357-101331877	K562	blood:	n/a	chr7:101331769-101331789
16	BACH1	chr7:101386578-101386843	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr7:101331570-101331859	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr7:101386557-101386766	K562	blood:	n/a	n/a
19	BATF	chr7:101306513-101306738	GM12878	blood:	n/a	n/a
20	BATF	chr7:101383102-101383413	GM12878	blood:	n/a	chr7:101383245-101383255
21	BCL3	chr7:101330460-101330767	GM12878	blood:	n/a	n/a
22	BCL3	chr7:101330491-101330901	GM12878	blood:	n/a	chr7:101330871-101330880
23	BCLAF1	chr7:101390338-101390733	GM12878	blood:	n/a	n/a
24	BCLAF1	chr7:101331518-101332013	GM12878	blood:	n/a	n/a
25	BHLHE40	chr7:101387326-101387494	K562	blood:	n/a	n/a
26	BHLHE40	chr7:101389694-101389888	GM12878	blood:	n/a	n/a
27	BHLHE40	chr7:101331586-101331991	HepG2	liver:	n/a	n/a
28	BHLHE40	chr7:101383150-101383255	K562	blood:	n/a	n/a
29	BHLHE40	chr7:101345701-101346003	K562	blood:	n/a	n/a
30	BHLHE40	chr7:101336841-101337430	HepG2	liver:	n/a	n/a
31	BHLHE40	chr7:101386556-101387082	K562	blood:	n/a	chr7:101386909-101386925 chr7:101386951-101386967
32	BHLHE40	chr7:101335283-101335408	GM12878	blood:	n/a	chr7:101335374-101335390
33	BHLHE40	chr7:101386503-101387000	GM12878	blood:	n/a	chr7:101386909-101386925 chr7:101386951-101386967
34	BHLHE40	chr7:101331415-101331958	K562	blood:	n/a	n/a
35	BHLHE40	chr7:101345629-101346079	HepG2	liver:	n/a	n/a
36	BHLHE40	chr7:101360992-101361665	HepG2	liver:	n/a	n/a
37	BHLHE40	chr7:101245701-101246022	GM12878	blood:	n/a	n/a
38	BHLHE40	chr7:101381274-101381486	K562	blood:	n/a	n/a
39	BHLHE40	chr7:101372586-101373272	K562	blood:	n/a	n/a
40	BHLHE40	chr7:101361569-101361698	GM12878	blood:	n/a	n/a
41	BHLHE40	chr7:101376973-101377338	K562	blood:	n/a	chr7:101377263-101377279
42	BHLHE40	chr7:101352437-101352579	K562	blood:	n/a	n/a
43	BHLHE40	chr7:101387657-101387690	GM12878	blood:	n/a	n/a
44	BHLHE40	chr7:101245709-101246072	K562	blood:	n/a	n/a
45	BHLHE40	chr7:101367311-101367398	K562	blood:	n/a	n/a
46	BHLHE40	chr7:101333452-101333663	HepG2	liver:	n/a	n/a
47	BHLHE40	chr7:101331544-101331946	GM12878	blood:	n/a	n/a
48	BHLHE40	chr7:101384304-101384641	GM12878	blood:	n/a	n/a
49	BRCA1	chr7:101361630-101361638	HepG2	liver:	n/a	n/a
50	BRCA1	chr7:101372545-101373221	Hela-S3	cervix:	n/a	n/a

(count:1831 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:101272515-101272565	PANC-1	pancreas:	n/a
2	chr7:101272515-101272565	PANC-1	pancreas:	n/a
3	chr7:101328918-101328968	HPAEpiC	pulmonary alveolar:	n/a
4	chr7:101384349-101384399	BE2_C	brain:	n/a
5	chr7:101364176-101364226	A549	lung:	n/a
6	chr7:101274027-101274077	HRE	kidney:	n/a
7	chr7:101273741-101273791	U87	brain:	n/a
8	chr7:101274027-101274077	U87	brain:	n/a
9	chr7:101361745-101361795	BJ	skin:	n/a
10	chr7:101364176-101364226	HIPEpiC	eye:	n/a
11	chr7:101331866-101331916	GM19239	blood:	n/a
12	chr7:101272582-101272632	AG04449	skin:	fetal
13	chr7:101385620-101385670	HCT-116	colon:	n/a
14	chr7:101274037-101274087	HEK293	kidney:	embryo
15	chr7:101335435-101335485	SAEC	small airway:	n/a
16	chr7:101257675-101257725	AG10803	skin:	n/a
17	chr7:101330867-101330917	AG04449	skin:	fetal
18	chr7:101386679-101386729	H1-hESC	embryonic stem cell:	embryo
19	chr7:101361745-101361795	NT2-D1	testis:	n/a
20	chr7:101257675-101257725	HCF	heart:	n/a
21	chr7:101274027-101274077	PANC-1	pancreas:	n/a
22	chr7:101331643-101331693	NH-A	brain:	n/a
23	chr7:101386951-101387001	AG04450	lung:	fetal
24	chr7:101384349-101384399	U87	brain:	n/a
25	chr7:101384349-101384399	SKMC	muscle:	n/a
26	chr7:101361745-101361795	MCF-7	breast:	n/a
27	chr7:101361527-101361577	SK-N-MC	brain:	n/a
28	chr7:101331866-101331916	SK-N-SH_RA	brain:	n/a
29	chr7:101375112-101375162	HCPEpiC	choroid plexus:	n/a
30	chr7:101273741-101273791	RPTEC	kidney:	n/a
31	chr7:101273741-101273791	NHBE	bronchial:	n/a
32	chr7:101272096-101272146	HPAEpiC	pulmonary alveolar:	n/a
33	chr7:101386951-101387001	SK-N-SH_RA	brain:	n/a
34	chr7:101331643-101331693	HAEpiC	amniotic membrane:	n/a
35	chr7:101335435-101335485	SKMC	muscle:	n/a
36	chr7:101272515-101272565	HCPEpiC	choroid plexus:	n/a
37	chr7:101331866-101331916	HRE	kidney:	n/a
38	chr7:101272582-101272632	HRE	kidney:	n/a
39	chr7:101361395-101361445	HIPEpiC	eye:	n/a
40	chr7:101390377-101390427	AG10803	skin:	n/a
41	chr7:101375112-101375162	Jurkat	blood:	n/a
42	chr7:101361395-101361445	NHBE	bronchial:	n/a
43	chr7:101386679-101386729	ProgFib	skin:	n/a
44	chr7:101330867-101330917	HNPCEpiC	eye:	n/a
45	chr7:101272484-101272534	PFSK-1	brain:	n/a
46	chr7:101328918-101328968	HRE	kidney:	n/a
47	chr7:101273741-101273791	AG09309	skin:	n/a
48	chr7:101386951-101387001	MCF10A-Er-Src	breast:	n/a
49	chr7:101387242-101387292	AoSMC	blood vessel:	n/a
50	chr7:101274037-101274087	T-47D	breast:	n/a

(count:203 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr7:101332498..101335096-chr7:101338388..101341217,2	MCF-7	breast:
2	chr7:101374945..101377506-chr7:101385778..101388397,3	K562	blood:
3	chr7:101240345..101242548-chr7:101441803..101443372,2	MCF-7	breast:
4	chr7:101232884..101235194-chr7:101237010..101238742,3	K562	blood:
5	chr7:101355519..101357844-chr7:101458933..101461181,2	MCF-7	breast:
6	chr7:101346607..101348692-chr7:101371323..101373114,2	MCF-7	breast:
7	chr7:101342424..101345349-chr7:101371267..101374522,4	MCF-7	breast:
8	chr7:101245631..101247804-chr7:101249820..101253085,4	MCF-7	breast:
9	chr7:101364262..101367929-chr7:101368962..101372975,5	MCF-7	breast:
10	chr7:101360472..101364691-chr7:101369638..101374194,4	K562	blood:
11	chr7:101386120..101387098-chr7:101458652..101459478,4	MCF-7	breast:
12	chr7:101345813..101348514-chr7:101359172..101361201,2	MCF-7	breast:
13	chr7:101245574..101246182-chr7:101331380..101332228,3	MCF-7	breast:
14	chr7:101330663..101332938-chr7:101456021..101458863,3	K562	blood:
15	chr7:101245559..101246104-chr7:101916727..101917460,2	K562	blood:
16	chr7:101363858..101366308-chr7:101375999..101378907,2	K562	blood:
17	chr7:101245451..101246297-chr7:101914933..101915725,2	MCF-7	breast:
18	chr7:101369100..101373067-chr7:101374919..101378261,3	K562	blood:
19	chr7:101343414..101344257-chr7:101647212..101647964,4	MCF-7	breast:
20	chr7:101360823..101364160-chr7:101364363..101367581,3	K562	blood:
21	chr7:101244039..101255564-chr7:101454524..101463981,21	MCF-7	breast:
22	chr7:101280631..101282500-chr7:101282807..101285513,2	MCF-7	breast:
23	chr7:101365806..101367484-chr7:101370262..101372822,3	K562	blood:
24	chr7:101230659..101232950-chr7:101241327..101243345,2	K562	blood:
25	chr7:101371362..101372936-chr7:101382706..101384319,2	MCF-7	breast:
26	chr7:101331189..101332041-chr7:101458655..101459223,2	NB4	blood:
27	chr7:101245468..101246352-chr7:101915597..101916163,4	K562	blood:
28	chr7:101363569..101367486-chr7:101367567..101371455,4	MCF-7	breast:
29	chr7:101386587..101387369-chr7:101458812..101459637,3	MCF-7	breast:
30	chr7:101272795..101275451-chr7:101277536..101279709,2	MCF-7	breast:
31	chr7:101232884..101235194-chr7:101237010..101238742,3	K562	blood:
32	chr7:101344423..101347351-chr7:101356075..101358287,2	MCF-7	breast:
33	chr7:101339021..101339937-chr7:101386563..101387082,2	MCF-7	breast:
34	chr7:101344423..101347351-chr7:101356075..101358287,2	MCF-7	breast:
35	chr7:101342279..101347280-chr7:101371204..101374879,9	MCF-7	breast:
36	chr7:101245091..101246357-chr7:101457101..101458459,9	MCF-7	breast:
37	chr7:101365013..101367690-chr7:101372321..101375439,3	MCF-7	breast:
38	chr7:101353778..101358971-chr7:101359540..101363864,5	MCF-7	breast:
39	chr7:101360823..101364160-chr7:101364363..101367581,3	K562	blood:
40	chr7:101371362..101372936-chr7:101382706..101384319,2	MCF-7	breast:
41	chr7:101392445..101394259-chr7:101445144..101446903,2	MCF-7	breast:
42	chr7:101342072..101344254-chr7:101386656..101389051,3	MCF-7	breast:
43	chr7:101331101..101332335-chr7:101879641..101880410,8	K562	blood:
44	chr7:101369491..101371079-chr7:101371516..101374342,2	MCF-7	breast:
45	chr7:101237649..101239948-chr7:101241103..101242929,2	MCF-7	breast:
46	chr7:101248988..101252731-chr7:101456839..101459495,3	MCF-7	breast:
47	chr7:101331022..101333643-chr7:101341514..101343495,2	MCF-7	breast:
48	chr7:101361844..101362344-chr9:111758752..111759253,2	NB4	blood:
49	chr7:101341881..101343718-chr7:101375300..101377318,2	MCF-7	breast:
50	chr7:101353340..101356209-chr7:101367178..101370003,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CUX1-1	chr7:101382637-101382867	FPKM1_group_30082_transcript_1
2	lnc-CUX1-1	chr7:101383141-101383371	NONHSAT122472
3	lnc-CUX1-1	chr7:101382581-101382711	FPKM1_group_30082_transcript_1
4	lnc-CUX1-1	chr7:101382581-101382711	NONHSAT122472

No data

Variant related genes	Relation type
MYL10	TF binding region
MYL10	CpG island
ENSG00000236778	chromatin interactions
ENSG00000257923	chromatin interactions
ENSG00000102786	chromatin interactions
ENSG00000106436	chromatin interactions
ENSG00000214078	chromatin interactions
ENSG00000244462	chromatin interactions

Extended variants
information (count: 5186 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:5186 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184212637	chr7:101231462-101231463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs74902037	chr7:101231467-101231468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs115173022	chr7:101231549-101231550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs13226495	chr7:101231555-101231556	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs550026053	chr7:101231631-101231632	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs55995100	chr7:101231632-101231633	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs549513884	chr7:101231734-101231735	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs188620273	chr7:101231812-101231813	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs10276555	chr7:101231849-101231850	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs192721395	chr7:101231903-101231904	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs77580251	chr7:101231923-101231924	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs551852098	chr7:101231931-101231932	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs569074684	chr7:101231944-101231945	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs182115563	chr7:101231974-101231975	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs543409886	chr7:101231999-101232000	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs558379249	chr7:101232011-101232012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576826154	chr7:101232026-101232027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs372691855	chr7:101232067-101232068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs7790294	chr7:101232159-101232160	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs145795102	chr7:101232219-101232220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs537656689	chr7:101232253-101232254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs10247942	chr7:101232299-101232300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs187078969	chr7:101232319-101232320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs563213037	chr7:101232351-101232352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs531610136	chr7:101232426-101232427	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs550105307	chr7:101232431-101232432	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs560929721	chr7:101232460-101232461	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs144172555	chr7:101232464-101232465	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs532684267	chr7:101232469-101232470	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs554705684	chr7:101232488-101232489	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs528286117	chr7:101232525-101232526	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs536816671	chr7:101232537-101232538	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs548917297	chr7:101232549-101232550	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs574667414	chr7:101232575-101232576	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs146485093	chr7:101232577-101232578	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs536646821	chr7:101232629-101232630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs149086633	chr7:101232642-101232643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs576752846	chr7:101232643-101232644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs534749455	chr7:101232649-101232650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs13233231	chr7:101232674-101232675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs551745635	chr7:101232675-101232676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs58154986	chr7:101232701-101232702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs375420065	chr7:101232702-101232703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs368627278	chr7:101232710-101232711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs13245903	chr7:101232714-101232715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs546620171	chr7:101232754-101232755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs372013668	chr7:101232762-101232763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs71559417	chr7:101232852-101232853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs4729738	chr7:101232882-101232883	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs10251552	chr7:101232909-101232910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Cancer	19907438	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2308 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101227400-101235200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:101227600-101233400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr7:101227800-101231600	Enhancers	Fetal Intestine Small	intestine
4	chr7:101230000-101232400	Weak transcription	Placenta	Placenta
5	chr7:101230200-101231600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr7:101230400-101232600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr7:101231400-101232200	Enhancers	HepG2	liver
8	chr7:101231600-101231800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr7:101231600-101232200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr7:101231600-101232200	Enhancers	NHDF-Ad	bronchial
11	chr7:101231600-101232600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr7:101231800-101232000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr7:101232400-101232600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr7:101232400-101232600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr7:101232400-101234400	Enhancers	Placenta	Placenta
16	chr7:101232600-101232800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr7:101232600-101234000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr7:101233400-101233800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr7:101233400-101234200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr7:101233400-101234400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr7:101233600-101234200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr7:101233600-101234200	Enhancers	HMEC	breast
23	chr7:101233600-101234400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr7:101233600-101234800	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr7:101234000-101234200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr7:101234000-101234400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:101234000-101234600	Enhancers	Esophagus	oesophagus
28	chr7:101234200-101238000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr7:101234400-101235800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr7:101234400-101237000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr7:101235800-101236000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr7:101236000-101241600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr7:101238000-101238400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr7:101238200-101238400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr7:101239600-101241600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr7:101240400-101241200	Enhancers	HepG2	liver
37	chr7:101241200-101241400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr7:101241200-101242200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
39	chr7:101241200-101242200	Flanking Active TSS	HepG2	liver
40	chr7:101241200-101242400	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr7:101241200-101242400	Enhancers	HMEC	breast
42	chr7:101241200-101242600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr7:101241200-101242600	Enhancers	Fetal Intestine Small	intestine
44	chr7:101241200-101242600	Enhancers	Fetal Lung	lung
45	chr7:101241200-101242600	Enhancers	Pancreas	Pancrea
46	chr7:101241200-101242800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr7:101241200-101242800	Enhancers	Placenta Amnion	Placenta Amnion
48	chr7:101241200-101242800	Enhancers	Stomach Mucosa	stomach
49	chr7:101241200-101243200	Enhancers	Fetal Muscle Leg	muscle
50	chr7:101241400-101241800	Enhancers	Duodenum Mucosa	Duodenum

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