Variant report

Variant	nsv593695
Chromosome Location	chr4:10138470-10345548
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2432)
CpG islands
(count:671)
Chromatin interactive
region (count:286)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2432 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:10286746-10287065	K562	blood:	n/a	n/a
2	ARID3A	chr4:10171356-10172376	K562	blood:	n/a	n/a
3	ARID3A	chr4:10258670-10258802	K562	blood:	n/a	n/a
4	ARID3A	chr4:10206912-10207070	K562	blood:	n/a	n/a
5	ARID3A	chr4:10242016-10242400	K562	blood:	n/a	n/a
6	ARID3A	chr4:10175936-10176225	K562	blood:	n/a	n/a
7	ARID3A	chr4:10206944-10207053	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:10186847-10188023	K562	blood:	n/a	n/a
9	ARID3A	chr4:10159442-10159716	K562	blood:	n/a	n/a
10	ARID3A	chr4:10182036-10184108	K562	blood:	n/a	n/a
11	ARID3A	chr4:10202441-10202778	K562	blood:	n/a	n/a
12	ARID3A	chr4:10188308-10188961	K562	blood:	n/a	n/a
13	ARID3A	chr4:10327415-10328296	K562	blood:	n/a	n/a
14	ARID3A	chr4:10174858-10175646	K562	blood:	n/a	n/a
15	ARID3A	chr4:10185222-10185607	K562	blood:	n/a	chr4:10185454-10185470
16	ARID3A	chr4:10172580-10173201	K562	blood:	n/a	n/a
17	ARID3A	chr4:10241023-10241142	K562	blood:	n/a	n/a
18	ATF1	chr4:10174911-10175439	K562	blood:	n/a	n/a
19	ATF1	chr4:10159418-10159720	K562	blood:	n/a	n/a
20	ATF1	chr4:10187244-10187892	K562	blood:	n/a	n/a
21	ATF1	chr4:10184693-10185042	K562	blood:	n/a	n/a
22	ATF1	chr4:10171263-10171804	K562	blood:	n/a	n/a
23	ATF1	chr4:10199601-10200004	K562	blood:	n/a	n/a
24	ATF1	chr4:10188186-10188661	K562	blood:	n/a	n/a
25	ATF1	chr4:10327430-10328176	K562	blood:	n/a	n/a
26	ATF1	chr4:10241521-10242349	K562	blood:	n/a	n/a
27	ATF1	chr4:10172681-10173016	K562	blood:	n/a	n/a
28	ATF1	chr4:10182216-10183403	K562	blood:	n/a	n/a
29	ATF2	chr4:10152775-10153075	GM12878	blood:	n/a	n/a
30	ATF2	chr4:10159305-10159743	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr4:10159321-10159751	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF3	chr4:10159392-10159666	K562	blood:	n/a	chr4:10159502-10159515
33	ATF3	chr4:10286691-10286995	K562	blood:	n/a	n/a
34	ATF3	chr4:10174879-10175394	K562	blood:	n/a	n/a
35	ATF3	chr4:10187352-10187768	K562	blood:	n/a	n/a
36	ATF3	chr4:10241484-10241931	K562	blood:	n/a	chr4:10241683-10241696
37	ATF3	chr4:10182376-10183375	K562	blood:	n/a	n/a
38	BACH1	chr4:10258150-10258286	K562	blood:	n/a	n/a
39	BACH1	chr4:10236419-10236458	K562	blood:	n/a	n/a
40	BACH1	chr4:10277398-10277423	K562	blood:	n/a	n/a
41	BACH1	chr4:10159277-10159771	K562	blood:	n/a	n/a
42	BACH1	chr4:10306752-10306755	K562	blood:	n/a	n/a
43	BACH1	chr4:10203548-10203807	K562	blood:	n/a	n/a
44	BACH1	chr4:10296613-10296622	K562	blood:	n/a	n/a
45	BACH1	chr4:10291449-10291596	K562	blood:	n/a	n/a
46	BACH1	chr4:10182278-10183266	K562	blood:	n/a	n/a
47	BACH1	chr4:10174959-10175395	K562	blood:	n/a	n/a
48	BACH1	chr4:10185169-10185293	K562	blood:	n/a	n/a
49	BACH1	chr4:10166286-10166294	K562	blood:	n/a	n/a
50	BACH1	chr4:10187292-10187596	K562	blood:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10299145-10299195	SKMC	muscle:	n/a
2	chr4:10147038-10147088	GM19239	blood:	n/a
3	chr4:10147038-10147088	GM12878	blood:	n/a
4	chr4:10160060-10160110	HCF	heart:	n/a
5	chr4:10143053-10143103	AG04450	lung:	fetal
6	chr4:10143053-10143103	NHDF-neo	bronchial:	n/a
7	chr4:10147038-10147088	RPTEC	kidney:	n/a
8	chr4:10160060-10160110	BE2_C	brain:	n/a
9	chr4:10147038-10147088	SAEC	small airway:	n/a
10	chr4:10160060-10160110	ovcar-3	ovarian:	n/a
11	chr4:10145483-10145533	GM19239	blood:	n/a
12	chr4:10145483-10145533	GM06990	blood:	n/a
13	chr4:10147100-10147150	Hela-S3	cervix:	n/a
14	chr4:10147100-10147150	NHBE	bronchial:	n/a
15	chr4:10147100-10147150	HUVEC	blood vessel:	n/a
16	chr4:10147330-10147380	AG04450	lung:	fetal
17	chr4:10143053-10143103	PrEC	prostate:	n/a
18	chr4:10147330-10147380	AG09309	skin:	n/a
19	chr4:10147606-10147656	AG04449	skin:	fetal
20	chr4:10335492-10335542	AG09309	skin:	n/a
21	chr4:10147302-10147352	CMK	blood:	n/a
22	chr4:10147606-10147656	HepG2	liver:	n/a
23	chr4:10143053-10143103	SKMC	muscle:	n/a
24	chr4:10143053-10143103	HepG2	liver:	n/a
25	chr4:10145483-10145533	HCM	heart:	n/a
26	chr4:10147100-10147150	HL-60	blood:	n/a
27	chr4:10147606-10147656	HAEpiC	amniotic membrane:	n/a
28	chr4:10147038-10147088	AG09319	gingival:	n/a
29	chr4:10147330-10147380	HMEC	breast:	n/a
30	chr4:10147606-10147656	K562	blood:	n/a
31	chr4:10335492-10335542	Jurkat	blood:	n/a
32	chr4:10149849-10149899	AG10803	skin:	n/a
33	chr4:10145483-10145533	ProgFib	skin:	n/a
34	chr4:10147606-10147656	Caco-2	colon:	n/a
35	chr4:10147100-10147150	U87	brain:	n/a
36	chr4:10147330-10147380	SK-N-MC	brain:	n/a
37	chr4:10147606-10147656	A549	lung:	n/a
38	chr4:10143053-10143103	MCF-7	breast:	n/a
39	chr4:10147100-10147150	A549	lung:	n/a
40	chr4:10147606-10147656	T-47D	breast:	n/a
41	chr4:10145483-10145533	CMK	blood:	n/a
42	chr4:10145483-10145533	T-47D	breast:	n/a
43	chr4:10147606-10147656	CMK	blood:	n/a
44	chr4:10147606-10147656	LNCaP	prostate:	n/a
45	chr4:10147330-10147380	HRPEpiC	eye:	n/a
46	chr4:10147330-10147380	CMK	blood:	n/a
47	chr4:10335492-10335542	Hela-S3	cervix:	n/a
48	chr4:10147330-10147380	NB4	blood:	n/a
49	chr4:10147606-10147656	HIPEpiC	eye:	n/a
50	chr4:10147038-10147088	H1-hESC	embryonic stem cell:	embryo

(count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr4:10187220..10189194-chr4:10403510..10406450,3	K562	blood:
2	chr4:10242448..10244811-chr4:10340269..10342798,2	K562	blood:
3	chr4:10249783..10252189-chr4:10254326..10257178,3	K562	blood:
4	chr4:10271663..10274322-chr4:10278537..10280895,2	K562	blood:
5	chr4:10254361..10256671-chr4:10262474..10264248,2	K562	blood:
6	chr4:10118560..10120526-chr4:10203986..10206288,3	K562	blood:
7	chr4:10326481..10328401-chr4:10338341..10340263,2	K562	blood:
8	chr4:10158010..10160333-chr4:10437817..10440737,2	K562	blood:
9	chr4:10147623..10149514-chr4:10156130..10157999,2	K562	blood:
10	chr4:10160529..10162216-chr4:10164137..10166713,2	K562	blood:
11	chr4:10181069..10182933-chr4:10345413..10347984,3	K562	blood:
12	chr4:10182491..10184302-chr4:10237283..10239761,2	K562	blood:
13	chr4:10181502..10184182-chr4:38665329..38667544,2	K562	blood:
14	chr4:10117458..10122489-chr4:10158161..10162241,5	MCF-7	breast:
15	chr4:10182494..10184635-chr4:10284696..10287291,2	K562	blood:
16	chr4:10329017..10330933-chr4:10334130..10336518,2	K562	blood:
17	chr4:10171114..10171975-chr4:10185300..10186046,2	K562	blood:
18	chr4:10151902..10153544-chr4:10159740..10162552,2	K562	blood:
19	chr4:10142468..10145387-chr4:10146611..10148310,2	MCF-7	breast:
20	chr4:10288926..10293598-chr4:10293770..10299284,5	K562	blood:
21	chr4:10147647..10149912-chr4:10150747..10153139,2	K562	blood:
22	chr4:10114665..10116599-chr4:10227448..10229354,2	K562	blood:
23	chr4:10173721..10176602-chr4:10326116..10328946,2	K562	blood:
24	chr4:10329017..10330933-chr4:10334130..10336518,2	K562	blood:
25	chr4:10185102..10187379-chr4:10256972..10258730,2	K562	blood:
26	chr4:10278587..10280479-chr4:10297418..10299087,2	K562	blood:
27	chr4:10182435..10184114-chr4:10441654..10444481,2	K562	blood:
28	chr4:10335054..10336642-chr4:10451338..10453609,2	K562	blood:
29	chr4:10186685..10189037-chr4:10459555..10461188,2	K562	blood:
30	chr4:10140012..10142690-chr4:10152544..10154199,2	K562	blood:
31	chr4:10166189..10167113-chr4:10551000..10552086,3	MCF-7	breast:
32	chr4:10321044..10322655-chr4:10326498..10328725,2	K562	blood:
33	chr4:10140012..10142690-chr4:10152544..10154199,2	K562	blood:
34	chr4:10200377..10202730-chr4:10225143..10227711,2	K562	blood:
35	chr19:17416908..17417590-chr4:10322243..10323174,2	Hela-S3	cervix:
36	chr4:10141623..10144820-chr4:10145857..10148531,3	K562	blood:
37	chr4:10240628..10243680-chr4:10247596..10249776,3	K562	blood:
38	chr4:10118040..10120090-chr4:10149414..10151081,2	K562	blood:
39	chr4:10300976..10303713-chr4:10304138..10305960,3	K562	blood:
40	chr4:10204306..10206166-chr4:10241229..10242983,2	K562	blood:
41	chr4:10159186..10164011-chr4:10164137..10169302,8	K562	blood:
42	chr4:10301025..10303713-chr4:10304138..10305960,2	K562	blood:
43	chr4:10298581..10300458-chr4:10305111..10307586,2	K562	blood:
44	chr4:10326554..10329109-chr4:10347770..10349654,2	K562	blood:
45	chr4:10181799..10184639-chr4:10262185..10264664,2	K562	blood:
46	chr4:10119978..10123045-chr4:10320529..10323793,3	K562	blood:
47	chr4:10173721..10176602-chr4:10326116..10328946,2	K562	blood:
48	chr4:10117542..10119864-chr4:10151862..10154716,2	MCF-7	breast:
49	chr4:10156172..10158401-chr4:10178392..10179954,2	K562	blood:
50	chr4:10146309..10149123-chr4:10156130..10158993,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR1-9	chr4:10256550-10258245	NONHSAT095490
2	lnc-WDR1-4	chr4:10151989-10152058	NONHSAT095472
3	lnc-WDR1-7	chr4:10201447-10202296	NONHSAT095488
4	lnc-WDR1-6	chr4:10168783-10169389	NONHSAT095487
5	lnc-WDR1-10	chr4:10261069-10261762	NONHSAT095491
6	lnc-WDR1-2	chr4:10144991-10145279	NONHSAT095429
7	lnc-ZNF518B-3	chr4:10286585-10287332	NONHSAT095493
8	lnc-ZNF518B-2	chr4:10293819-10294332	NONHSAT095494
9	lnc-WDR1-11	chr4:10269519-10269855	NONHSAT095492
10	lnc-WDR1-4	chr4:10159007-10159491	NONHSAT095472

No data

Variant related genes	Relation type
ENSG00000248777	TF binding region
ENSG00000251338	TF binding region
ENSG00000271544	TF binding region
ENSG00000250040	TF binding region
ENSG00000251296	TF binding region
ENSG00000250074	TF binding region
ENSG00000251278	TF binding region
ENSG00000250573	TF binding region
ENSG00000250505	TF binding region
ENSG00000250393	TF binding region
ENSG00000248777	CpG island
ENSG00000251338	CpG island
ENSG00000271544	CpG island
ENSG00000250040	CpG island
ENSG00000251296	CpG island
ENSG00000250074	CpG island
ENSG00000251278	CpG island
ENSG00000250573	CpG island
ENSG00000250505	CpG island
ENSG00000250393	CpG island
ENSG00000251296	chromatin interactions
ENSG00000248777	chromatin interactions
ENSG00000196355	chromatin interactions
ENSG00000109787	chromatin interactions
ENSG00000251278	chromatin interactions
ENSG00000250573	chromatin interactions
ENSG00000271544	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000250393	chromatin interactions
ENSG00000251338	chromatin interactions
ENSG00000178163	chromatin interactions
ENSG00000223086	chromatin interactions
ENSG00000250040	chromatin interactions
ENSG00000231160	chromatin interactions

Extended variants
information (count: 13989 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:13989 , 50 per page) page: 1 2 3 4 5 6 7 ... 280

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17198113	chr4:10138470-10138471	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs192787533	chr4:10138481-10138482	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs111950017	chr4:10138494-10138495	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs553467868	chr4:10138496-10138497	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs55696151	chr4:10138510-10138511	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs79841358	chr4:10138511-10138512	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs566013141	chr4:10138514-10138515	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs536541445	chr4:10138518-10138519	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs372198966	chr4:10138529-10138530	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs183594965	chr4:10138540-10138541	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs576261599	chr4:10138561-10138562	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs189513412	chr4:10138563-10138564	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs556588697	chr4:10138570-10138571	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs192310561	chr4:10138575-10138576	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs549848415	chr4:10138581-10138582	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs112695895	chr4:10138601-10138602	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs560275124	chr4:10138608-10138609	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs527984195	chr4:10138621-10138622	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs542866402	chr4:10138698-10138699	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs138469361	chr4:10138704-10138705	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs531754868	chr4:10138707-10138708	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs550089454	chr4:10138721-10138722	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs11732828	chr4:10138746-10138747	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs532105519	chr4:10138747-10138748	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs547410313	chr4:10138758-10138759	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs565499149	chr4:10138762-10138763	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs536557366	chr4:10138768-10138769	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs554878529	chr4:10138769-10138770	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs374452404	chr4:10138775-10138776	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs569883153	chr4:10138779-10138780	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs184371249	chr4:10138784-10138785	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs113067629	chr4:10138798-10138799	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs113903254	chr4:10138801-10138802	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs74603183	chr4:10138811-10138812	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs190129750	chr4:10138813-10138814	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs572079831	chr4:10138815-10138816	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs115259380	chr4:10138825-10138826	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs11726982	chr4:10138848-10138849	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs561279015	chr4:10138857-10138858	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs75194906	chr4:10138863-10138864	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs186704005	chr4:10138872-10138873	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs138813204	chr4:10138883-10138884	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs529451163	chr4:10138884-10138885	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs565329014	chr4:10138893-10138894	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs62287521	chr4:10138894-10138895	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs547131169	chr4:10138902-10138903	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs111302286	chr4:10138916-10138917	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs529682618	chr4:10138919-10138920	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs62287522	chr4:10138920-10138921	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs570010661	chr4:10138926-10138927	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1125 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10142400-10142800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr4:10142600-10142800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr4:10142600-10143000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:10142600-10143200	Enhancers	Fetal Thymus	thymus
5	chr4:10142800-10143000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
6	chr4:10142800-10143200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr4:10142800-10143200	Enhancers	H1 Cell Line	embryonic stem cell
8	chr4:10142800-10143200	Enhancers	H9 Cell Line	embryonic stem cell
9	chr4:10142800-10143200	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr4:10142800-10143200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
11	chr4:10142800-10151800	Weak transcription	Spleen	Spleen
12	chr4:10143000-10143200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr4:10143000-10143200	Active TSS	HUES48 Cell Line	embryonic stem cell
14	chr4:10143000-10143200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr4:10143000-10143200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr4:10143200-10143600	Enhancers	Rectal Mucosa Donor 29	rectum
17	chr4:10143200-10149800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr4:10146200-10147000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr4:10146400-10146800	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr4:10146400-10147000	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr4:10146400-10147000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr4:10146400-10147600	Enhancers	Primary B cells from peripheral blood	blood
23	chr4:10146600-10147200	Bivalent Enhancer	Primary B cells from cord blood	blood
24	chr4:10149800-10150000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr4:10151000-10151200	Enhancers	Fetal Stomach	stomach
26	chr4:10151200-10164400	Weak transcription	Right Atrium	heart
27	chr4:10151400-10152400	Weak transcription	Fetal Stomach	stomach
28	chr4:10151800-10152000	Enhancers	Spleen	Spleen
29	chr4:10151800-10153000	Enhancers	Fetal Muscle Leg	muscle
30	chr4:10152000-10152200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
31	chr4:10152000-10153600	Enhancers	Primary B cells from cord blood	blood
32	chr4:10152200-10153800	Enhancers	Primary B cells from peripheral blood	blood
33	chr4:10152400-10152800	Enhancers	Fetal Stomach	stomach
34	chr4:10152600-10152800	Flanking Active TSS	GM12878-XiMat	blood
35	chr4:10152800-10153400	Enhancers	GM12878-XiMat	blood
36	chr4:10156800-10157000	Bivalent Enhancer	HSMMtube	muscle
37	chr4:10157600-10157800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
38	chr4:10157600-10160800	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr4:10158000-10160800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr4:10158600-10160000	Enhancers	Thymus	Thymus
41	chr4:10158600-10165600	Enhancers	Fetal Thymus	thymus
42	chr4:10158800-10159800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr4:10158800-10161000	Enhancers	Fetal Stomach	stomach
44	chr4:10158800-10161200	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr4:10159000-10160200	Enhancers	Brain Angular Gyrus	brain
46	chr4:10159000-10160800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
47	chr4:10159000-10160800	Enhancers	Brain Hippocampus Middle	brain
48	chr4:10159000-10160800	Enhancers	Brain Substantia Nigra	brain
49	chr4:10159200-10159400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr4:10159200-10159400	Enhancers	Brain Inferior Temporal Lobe	brain

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