Variant report

Variant	esv3327487
Chromosome Location	chr7:84901505-85320690
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1581)
CpG islands
(count:489)
Chromatin interactive
region (count:37)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1581 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:85183644-85184017	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:85104858-85105209	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:85044798-85045544	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:85055557-85056303	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:85046963-85047244	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:85194316-85194431	HepG2	liver:	n/a	n/a
7	ATF1	chr7:85100263-85100337	K562	blood:	n/a	n/a
8	ATF1	chr7:85183590-85183761	K562	blood:	n/a	n/a
9	ATF1	chr7:84946020-84946102	K562	blood:	n/a	n/a
10	ATF1	chr7:85210707-85210842	K562	blood:	n/a	n/a
11	ATF1	chr7:85142385-85142483	K562	blood:	n/a	n/a
12	ATF2	chr7:85103479-85103831	GM12878	blood:	n/a	n/a
13	BACH1	chr7:85077761-85077773	K562	blood:	n/a	n/a
14	BACH1	chr7:85229703-85230012	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr7:85103539-85103766	GM12878	blood:	n/a	n/a
16	BATF	chr7:84972886-84973042	GM12878	blood:	n/a	n/a
17	BATF	chr7:85101094-85101354	GM12878	blood:	n/a	n/a
18	BATF	chr7:85103571-85103842	GM12878	blood:	n/a	chr7:85103811-85103820
19	BCL3	chr7:85221189-85221679	A549	lung:	n/a	n/a
20	BHLHE40	chr7:85183697-85183834	K562	blood:	n/a	n/a
21	BHLHE40	chr7:85045189-85045320	HepG2	liver:	n/a	n/a
22	BHLHE40	chr7:84922251-84922904	GM12878	blood:	n/a	n/a
23	BHLHE40	chr7:85055776-85056346	HepG2	liver:	n/a	n/a
24	BHLHE40	chr7:84918375-84918822	HepG2	liver:	n/a	n/a
25	BHLHE40	chr7:85221305-85221476	HepG2	liver:	n/a	n/a
26	BRCA1	chr7:85056041-85056112	HepG2	liver:	n/a	n/a
27	CCNT2	chr7:85016458-85016593	K562	blood:	n/a	n/a
28	CCNT2	chr7:85231581-85231835	K562	blood:	n/a	n/a
29	CEBPB	chr7:85097511-85097798	HepG2	liver:	n/a	chr7:85097670-85097681
30	CEBPB	chr7:85277952-85278313	HepG2	liver:	n/a	chr7:85278124-85278135
31	CEBPB	chr7:85184148-85184492	HepG2	liver:	n/a	chr7:85184415-85184426 chr7:85184308-85184321 chr7:85184309-85184320 chr7:85184415-85184428 chr7:85184415-85184426
32	CEBPB	chr7:85112580-85112982	IMR90	lung:	n/a	chr7:85112763-85112774 chr7:85112762-85112775
33	CEBPB	chr7:85260254-85260658	A549	lung:	n/a	n/a
34	CEBPB	chr7:85158610-85158946	IMR90	lung:	n/a	n/a
35	CEBPB	chr7:85067006-85067267	IMR90	lung:	n/a	chr7:85067120-85067131 chr7:85067122-85067133 chr7:85067120-85067133 chr7:85067122-85067131
36	CEBPB	chr7:85277974-85278295	IMR90	lung:	n/a	chr7:85278124-85278135
37	CEBPB	chr7:85018669-85018940	Hela-S3	cervix:	n/a	chr7:85018791-85018802 chr7:85018793-85018802
38	CEBPB	chr7:85183600-85183934	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr7:85097504-85097820	IMR90	lung:	n/a	chr7:85097670-85097681
40	CEBPB	chr7:84901231-84901542	HepG2	liver:	n/a	chr7:84901362-84901373 chr7:84901361-84901374 chr7:84901361-84901374
41	CEBPB	chr7:85184159-85184489	IMR90	lung:	n/a	chr7:85184415-85184426 chr7:85184308-85184321 chr7:85184309-85184320 chr7:85184415-85184428 chr7:85184415-85184426
42	CEBPB	chr7:85158711-85158903	HepG2	liver:	n/a	n/a
43	CEBPB	chr7:85112607-85112957	HepG2	liver:	n/a	chr7:85112763-85112774 chr7:85112762-85112775
44	CEBPB	chr7:85144481-85144935	IMR90	lung:	n/a	chr7:85144775-85144786
45	CEBPB	chr7:85087413-85087769	IMR90	lung:	n/a	chr7:85087596-85087605 chr7:85087594-85087607 chr7:85087596-85087605 chr7:85087596-85087605 chr7:85087594-85087605 chr7:85087596-85087607 chr7:85087596-85087605 chr7:85087594-85087607 chr7:85087596-85087607 chr7:85087594-85087607
46	CEBPB	chr7:85260085-85260722	A549	lung:	n/a	n/a
47	CEBPB	chr7:85270505-85271102	Hela-S3	cervix:	n/a	chr7:85270598-85270609
48	CEBPB	chr7:85055704-85056676	HepG2	liver:	n/a	chr7:85056185-85056196
49	CEBPB	chr7:85056069-85056256	HepG2	liver:	n/a	chr7:85056185-85056196
50	CEBPB	chr7:85055686-85056382	HepG2	liver:	n/a	chr7:85056185-85056196

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:85010741-85010791	HL-60	blood:	n/a
2	chr7:85010741-85010791	HL-60	blood:	n/a
3	chr7:84904903-84904953	GM12891	blood:	n/a
4	chr7:85157964-85158014	ECC-1	luminal epithelium:	n/a
5	chr7:85010741-85010791	H1-hESC	embryonic stem cell:	embryo
6	chr7:85138606-85138656	Hela-S3	cervix:	n/a
7	chr7:84964803-84964853	HRE	kidney:	n/a
8	chr7:85138606-85138656	BE2_C	brain:	n/a
9	chr7:85157964-85158014	HMEC	breast:	n/a
10	chr7:84904903-84904953	SK-N-SH_RA	brain:	n/a
11	chr7:85010774-85010824	HL-60	blood:	n/a
12	chr7:85010676-85010726	HL-60	blood:	n/a
13	chr7:85151454-85151504	GM19239	blood:	n/a
14	chr7:85157964-85158014	AG04450	lung:	fetal
15	chr7:85010774-85010824	AG09309	skin:	n/a
16	chr7:84904903-84904953	NHBE	bronchial:	n/a
17	chr7:85010741-85010791	BJ	skin:	n/a
18	chr7:84964803-84964853	AG09319	gingival:	n/a
19	chr7:85010676-85010726	HepG2	liver:	n/a
20	chr7:85157964-85158014	SKMC	muscle:	n/a
21	chr7:84904903-84904953	HL-60	blood:	n/a
22	chr7:85010676-85010726	MCF-7	breast:	n/a
23	chr7:84904903-84904953	GM12892	blood:	n/a
24	chr7:85157964-85158014	IMR90	lung:	fetal
25	chr7:84964803-84964853	HepG2	liver:	n/a
26	chr7:84964803-84964853	Hela-S3	cervix:	n/a
27	chr7:84964803-84964853	PFSK-1	brain:	n/a
28	chr7:84964803-84964853	NH-A	brain:	n/a
29	chr7:85010774-85010824	GM12892	blood:	n/a
30	chr7:85010676-85010726	HEEpiC	esophagus:	n/a
31	chr7:84904903-84904953	AG09309	skin:	n/a
32	chr7:84964803-84964853	SKMC	muscle:	n/a
33	chr7:85010741-85010791	U87	brain:	n/a
34	chr7:85010741-85010791	ProgFib	skin:	n/a
35	chr7:84904903-84904953	HPAEpiC	pulmonary alveolar:	n/a
36	chr7:85010676-85010726	SKMC	muscle:	n/a
37	chr7:85010741-85010791	GM12891	blood:	n/a
38	chr7:84904903-84904953	Hepatocyte	liver:	n/a
39	chr7:85010774-85010824	BJ	skin:	n/a
40	chr7:85010676-85010726	NT2-D1	testis:	n/a
41	chr7:85010741-85010791	HCPEpiC	choroid plexus:	n/a
42	chr7:85151454-85151504	HCPEpiC	choroid plexus:	n/a
43	chr7:85010774-85010824	PrEC	prostate:	n/a
44	chr7:85010774-85010824	AG04450	lung:	fetal
45	chr7:85138606-85138656	AG09309	skin:	n/a
46	chr7:85138606-85138656	BJ	skin:	n/a
47	chr7:85138606-85138656	SK-N-SH_RA	brain:	n/a
48	chr7:85010676-85010726	HNPCEpiC	eye:	n/a
49	chr7:85157964-85158014	SK-N-SH_RA	brain:	n/a
50	chr7:85138606-85138656	HMEC	breast:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:85283178..85285409-chr7:85295868..85298479,2	K562	blood:
2	chr7:85109548..85112253-chr7:85116384..85119002,2	K562	blood:
3	chr7:84973626..84975407-chr7:84976832..84979639,2	K562	blood:
4	chr7:85253799..85255323-chr7:85392933..85394931,2	K562	blood:
5	chr7:85134714..85136666-chr7:85145066..85147658,2	K562	blood:
6	chr7:84659480..84660360-chr7:85183314..85184162,2	MCF-7	breast:
7	chr7:85183273..85184394-chr7:85379037..85380205,4	MCF-7	breast:
8	chr7:85153959..85156643-chr7:85186340..85188558,2	K562	blood:
9	chr7:84914222..84917543-chr7:84917652..84920035,3	K562	blood:
10	chr7:85144834..85146430-chr7:85147566..85149706,2	K562	blood:
11	chr7:85224212..85226454-chr7:85229348..85230972,2	MCF-7	breast:
12	chr7:84670622..84671190-chr7:85183449..85184130,2	MCF-7	breast:
13	chr7:84671065..84671572-chr7:85183760..85184324,2	MCF-7	breast:
14	chr7:84973626..84975407-chr7:84976832..84979639,2	K562	blood:
15	chr7:84976573..84978423-chr7:84984780..84986370,2	K562	blood:
16	chr7:84921780..84923883-chr7:84923986..84925555,2	MCF-7	breast:
17	chr7:85153959..85156643-chr7:85186340..85188558,2	K562	blood:
18	chr12:7024083..7024583-chr7:85192420..85193063,2	MCF-7	breast:
19	chr7:85283178..85285409-chr7:85295868..85298479,2	K562	blood:
20	chr7:85005716..85007479-chr7:85012871..85015681,2	K562	blood:
21	chr7:85111683..85113494-chr7:85114215..85116329,2	MCF-7	breast:
22	chr7:85134714..85136666-chr7:85145066..85147658,2	K562	blood:
23	chr7:85308217..85310976-chr7:85319163..85322845,3	K562	blood:
24	chr7:84914222..84917543-chr7:84917652..84920035,3	K562	blood:
25	chr7:85315775..85319352-chr7:85321463..85324593,3	K562	blood:
26	chr7:84976573..84978423-chr7:84984780..84986370,2	K562	blood:
27	chr7:85144834..85146430-chr7:85147566..85149706,2	K562	blood:
28	chr7:85056336..85059058-chr7:85072984..85075218,2	K562	blood:
29	chr7:85111683..85113494-chr7:85114215..85116329,2	MCF-7	breast:
30	chr7:85005716..85007479-chr7:85012871..85015681,2	K562	blood:
31	chr7:85224212..85226454-chr7:85229348..85230972,2	MCF-7	breast:
32	chr7:85308217..85310976-chr7:85319163..85322845,3	K562	blood:
33	chr7:84922126..84922846-chr8:107469062..107469738,2	HCT-116	colon:
34	chr7:84921780..84923883-chr7:84923986..84925555,2	MCF-7	breast:
35	chr7:85109548..85112253-chr7:85116384..85119002,2	K562	blood:
36	chr7:85056336..85059058-chr7:85072984..85075218,2	K562	blood:
37	chr12:21268556..21269333-chr7:84915114..84915941,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEMA3D-4	chr7:85265329-85265660	NONHSAT121800
2	lnc-GRM3-1	chr7:85079176-85079305	XLOC_006160
3	lnc-GRM3-1	chr7:85050438-85050574	XLOC_006160
4	lnc-GRM3-1	chr7:85104568-85104676	XLOC_006160
5	lnc-GRM3-1	chr7:85118198-85118548	XLOC_006160
6	lnc-GRM3-1	chr7:85104543-85104676	XLOC_006160
7	lnc-GRM3-1	chr7:85118198-85118609	XLOC_006160

No data

Variant related genes	Relation type
ENSG00000227785	TF binding region
LINC00972	TF binding region
ENSG00000230614	TF binding region
ENSG00000227785	CpG island
LINC00972	CpG island
ENSG00000230614	CpG island
ENSG00000111674	chromatin interactions
ENSG00000153993	chromatin interactions
FAM135A	miRNA target sites

Extended variants
information (count: 8177 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:8177 , 50 per page) page: 1 2 3 4 5 6 7 ... 164

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188516211	chr7:84901505-84901506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs373850110	chr7:84901507-84901508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554154868	chr7:84901571-84901572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs79904061	chr7:84901575-84901576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539725565	chr7:84901585-84901586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539597632	chr7:84901594-84901595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558238533	chr7:84901617-84901618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576493989	chr7:84901646-84901647	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543825905	chr7:84901651-84901652	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562529356	chr7:84901652-84901653	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574334641	chr7:84901665-84901666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542145732	chr7:84901712-84901713	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148448148	chr7:84901713-84901714	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs202128153	chr7:84901722-84901723	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200544547	chr7:84901728-84901729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs527487005	chr7:84901744-84901745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552362469	chr7:84901748-84901749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547212824	chr7:84901770-84901771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73199719	chr7:84901828-84901829	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs193068071	chr7:84901869-84901870	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568477347	chr7:84901870-84901871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535473028	chr7:84901881-84901882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548072774	chr7:84901882-84901883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566200877	chr7:84901915-84901916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544332869	chr7:84902048-84902049	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372403512	chr7:84902051-84902052	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs77789223	chr7:84902058-84902059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184072553	chr7:84902068-84902069	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142618728	chr7:84902078-84902079	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576205826	chr7:84902087-84902088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537582141	chr7:84902165-84902166	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555974075	chr7:84902171-84902172	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574417728	chr7:84902205-84902206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201990629	chr7:84902212-84902213	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566949121	chr7:84902327-84902328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536005458	chr7:84902339-84902340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572338311	chr7:84902340-84902341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546044275	chr7:84902352-84902353	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555905982	chr7:84902353-84902354	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188381574	chr7:84902357-84902358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs180848331	chr7:84902405-84902406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs113648822	chr7:84902430-84902431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10238707	chr7:84902456-84902457	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs377560442	chr7:84902467-84902468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183791698	chr7:84902488-84902489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs547439817	chr7:84902496-84902497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs7779419	chr7:84902510-84902511	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs140654660	chr7:84902512-84902513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs551641243	chr7:84902532-84902533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs573461861	chr7:84902534-84902535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Williams-beuren syndrome	16826523	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Williams Syndrome	20824207	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:609 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:84892600-84902200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:84899400-84902400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr7:84901400-84902400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr7:84902200-84902400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr7:84902400-84904000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:84902400-84904600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr7:84902400-84906400	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr7:84902600-84904400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr7:84902600-84906400	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr7:84902600-84906400	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr7:84902800-84903200	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr7:84902800-84904400	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr7:84902800-84906400	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr7:84903200-84905000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr7:84903800-84904000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr7:84903800-84904200	Enhancers	H1 Cell Line	embryonic stem cell
17	chr7:84903800-84905200	Enhancers	H9 Cell Line	embryonic stem cell
18	chr7:84904000-84904800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr7:84904000-84905000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr7:84904000-84905000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr7:84904200-84905400	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr7:84904400-84904600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr7:84904400-84905200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr7:84904600-84906400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr7:84904600-84906400	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr7:84904800-84905200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr7:84905000-84905400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr7:84905000-84906000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
29	chr7:84905000-84906200	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr7:84905200-84905600	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr7:84905200-84906200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr7:84905200-84906400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr7:84905400-84906000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr7:84905400-84907000	Enhancers	H1 Cell Line	embryonic stem cell
35	chr7:84905600-84906200	Enhancers	H9 Cell Line	embryonic stem cell
36	chr7:84906200-84916000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr7:84909400-84910200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr7:84909800-84910200	Enhancers	Fetal Heart	heart
39	chr7:84910200-84911200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr7:84911200-84912000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr7:84912000-84916000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr7:84914600-84916400	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr7:84914600-84916800	Enhancers	Brain Substantia Nigra	brain
44	chr7:84914800-84915200	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr7:84914800-84916000	Enhancers	Brain Cingulate Gyrus	brain
46	chr7:84915000-84915200	Enhancers	Brain Hippocampus Middle	brain
47	chr7:84915000-84915200	Enhancers	Fetal Muscle Leg	muscle
48	chr7:84915000-84915400	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr7:84915200-84918200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr7:84915400-84916400	Weak transcription	Fetal Muscle Leg	muscle

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