Variant report

Variant	nsv550813
Chromosome Location	chr10:49669142-49735563
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1958)
CpG islands
(count:1833)
Chromatin interactive
region (count:132)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1958 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:49678782-49678981	K562	blood:	n/a	n/a
2	ARID3A	chr10:49732473-49732510	K562	blood:	n/a	n/a
3	ARID3A	chr10:49714573-49714848	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:49688764-49689166	K562	blood:	n/a	n/a
5	ARID3A	chr10:49713702-49713754	K562	blood:	n/a	n/a
6	ARID3A	chr10:49690130-49690749	K562	blood:	n/a	n/a
7	ARID3A	chr10:49692988-49693267	HepG2	liver:	n/a	n/a
8	ARID3A	chr10:49675990-49676555	K562	blood:	n/a	n/a
9	ARID3A	chr10:49678058-49678575	K562	blood:	n/a	n/a
10	ARID3A	chr10:49715145-49715390	HepG2	liver:	n/a	n/a
11	ARID3A	chr10:49693314-49694070	K562	blood:	n/a	n/a
12	ARID3A	chr10:49695333-49695513	K562	blood:	n/a	n/a
13	ARID3A	chr10:49714503-49714913	K562	blood:	n/a	n/a
14	ARID3A	chr10:49694926-49694938	K562	blood:	n/a	n/a
15	ARID3A	chr10:49691525-49691700	K562	blood:	n/a	n/a
16	ARID3A	chr10:49696119-49696245	K562	blood:	n/a	n/a
17	ATF1	chr10:49678117-49678704	K562	blood:	n/a	n/a
18	ATF1	chr10:49676060-49676637	K562	blood:	n/a	n/a
19	ATF3	chr10:49731160-49731399	K562	blood:	n/a	n/a
20	ATF3	chr10:49678060-49678521	K562	blood:	n/a	n/a
21	BACH1	chr10:49732288-49732597	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr10:49714441-49714585	K562	blood:	n/a	n/a
23	BACH1	chr10:49716040-49716159	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr10:49678049-49678348	K562	blood:	n/a	n/a
25	BACH1	chr10:49731254-49732056	H1-hESC	embryonic stem cell:	n/a	n/a
26	BCLAF1	chr10:49678066-49678625	K562	blood:	n/a	n/a
27	BCLAF1	chr10:49678021-49678701	K562	blood:	n/a	n/a
28	BHLHE40	chr10:49712840-49712973	K562	blood:	n/a	n/a
29	BHLHE40	chr10:49713518-49714275	K562	blood:	n/a	chr10:49714139-49714155
30	BHLHE40	chr10:49688905-49689423	K562	blood:	n/a	chr10:49689144-49689160
31	BHLHE40	chr10:49679261-49679734	K562	blood:	n/a	n/a
32	BHLHE40	chr10:49731803-49732672	K562	blood:	n/a	chr10:49732501-49732517
33	BHLHE40	chr10:49687839-49687843	K562	blood:	n/a	n/a
34	BHLHE40	chr10:49716230-49716334	K562	blood:	n/a	n/a
35	BHLHE40	chr10:49671706-49672073	K562	blood:	n/a	n/a
36	BHLHE40	chr10:49676985-49677380	K562	blood:	n/a	n/a
37	BHLHE40	chr10:49731901-49732129	HepG2	liver:	n/a	n/a
38	BHLHE40	chr10:49731989-49732177	GM12878	blood:	n/a	n/a
39	BHLHE40	chr10:49684621-49684929	K562	blood:	n/a	n/a
40	BHLHE40	chr10:49677764-49679018	K562	blood:	n/a	n/a
41	BHLHE40	chr10:49714483-49715086	K562	blood:	n/a	n/a
42	BHLHE40	chr10:49676218-49676569	K562	blood:	n/a	n/a
43	BHLHE40	chr10:49701167-49701229	K562	blood:	n/a	n/a
44	BHLHE40	chr10:49687235-49687354	K562	blood:	n/a	n/a
45	BHLHE40	chr10:49732047-49732051	A549	lung:	n/a	n/a
46	BHLHE40	chr10:49726095-49726324	GM12878	blood:	n/a	n/a
47	BHLHE40	chr10:49669772-49669965	K562	blood:	n/a	n/a
48	BRCA1	chr10:49714693-49714870	HepG2	liver:	n/a	n/a
49	CBX3	chr10:49721057-49721457	K562	blood:	n/a	n/a
50	CBX3	chr10:49722290-49722710	K562	blood:	n/a	n/a

(count:1833 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:49710976-49711026	PANC-1	pancreas:	n/a
2	chr10:49673534-49673584	PFSK-1	brain:	n/a
3	chr10:49687669-49687719	Hepatocyte	liver:	n/a
4	chr10:49710976-49711026	PANC-1	pancreas:	n/a
5	chr10:49673534-49673584	PFSK-1	brain:	n/a
6	chr10:49687669-49687719	Hepatocyte	liver:	n/a
7	chr10:49699321-49699371	GM12892	blood:	n/a
8	chr10:49730753-49730803	BE2_C	brain:	n/a
9	chr10:49731375-49731425	ovcar-3	ovarian:	n/a
10	chr10:49732637-49732687	BJ	skin:	n/a
11	chr10:49732315-49732365	AG04450	lung:	fetal
12	chr10:49674348-49674398	GM12892	blood:	n/a
13	chr10:49674883-49674933	MCF-7	breast:	n/a
14	chr10:49732003-49732053	HMEC	breast:	n/a
15	chr10:49687869-49687919	PrEC	prostate:	n/a
16	chr10:49674458-49674508	CMK	blood:	n/a
17	chr10:49691166-49691216	HL-60	blood:	n/a
18	chr10:49687869-49687919	RPTEC	kidney:	n/a
19	chr10:49674251-49674301	HMEC	breast:	n/a
20	chr10:49733339-49733389	AoSMC	blood vessel:	n/a
21	chr10:49732315-49732365	NH-A	brain:	n/a
22	chr10:49671665-49671715	HEEpiC	esophagus:	n/a
23	chr10:49730753-49730803	CMK	blood:	n/a
24	chr10:49732637-49732687	MCF-7	breast:	n/a
25	chr10:49732003-49732053	LNCaP	prostate:	n/a
26	chr10:49710976-49711026	BJ	skin:	n/a
27	chr10:49688893-49688943	SK-N-MC	brain:	n/a
28	chr10:49684658-49684708	SK-N-SH_RA	brain:	n/a
29	chr10:49716328-49716378	HepG2	liver:	n/a
30	chr10:49732315-49732365	PANC-1	pancreas:	n/a
31	chr10:49687669-49687719	A549	lung:	n/a
32	chr10:49673534-49673584	HRE	kidney:	n/a
33	chr10:49705591-49705641	K562	blood:	n/a
34	chr10:49734874-49734924	SK-N-MC	brain:	n/a
35	chr10:49674530-49674580	HCT-116	colon:	n/a
36	chr10:49730753-49730803	PFSK-1	brain:	n/a
37	chr10:49705591-49705641	GM12891	blood:	n/a
38	chr10:49684658-49684708	HUVEC	blood vessel:	n/a
39	chr10:49705591-49705641	MCF10A-Er-Src	breast:	n/a
40	chr10:49678358-49678408	HMEC	breast:	n/a
41	chr10:49728916-49728966	HRCEpiC	kidney:	n/a
42	chr10:49671665-49671715	BJ	skin:	n/a
43	chr10:49674458-49674508	HUVEC	blood vessel:	n/a
44	chr10:49674530-49674580	AoSMC	blood vessel:	n/a
45	chr10:49730753-49730803	HIPEpiC	eye:	n/a
46	chr10:49716328-49716378	ECC-1	luminal epithelium:	n/a
47	chr10:49674251-49674301	GM06990	blood:	n/a
48	chr10:49674458-49674508	RPTEC	kidney:	n/a
49	chr10:49688893-49688943	IMR90	lung:	fetal
50	chr10:49674348-49674398	K562	blood:	n/a

(count:132 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr10:49735319..49737955-chr10:49741189..49744071,3	K562	blood:
2	chr10:49692340..49695073-chr10:49708069..49710836,2	K562	blood:
3	chr10:49676784..49678693-chr10:49717036..49719541,2	K562	blood:
4	chr10:49571458..49572711-chr10:49713545..49714151,3	MCF-7	breast:
5	chr10:49571896..49573651-chr10:49713045..49714727,3	K562	blood:
6	chr10:49723375..49726156-chr10:49734098..49735696,2	K562	blood:
7	chr10:49711695..49713826-chr10:49717716..49719906,2	K562	blood:
8	chr10:49725693..49727830-chr10:49743883..49745489,2	K562	blood:
9	chr10:49715021..49718761-chr10:49720982..49725227,3	K562	blood:
10	chr10:49714336..49715131-chr17:58308612..58309289,2	MCF-7	breast:
11	chr10:49698265..49700401-chr10:49714707..49717015,2	K562	blood:
12	chr10:49653089..49653710-chr10:49671711..49672225,2	MCF-7	breast:
13	chr10:49714456..49715089-chr10:49863805..49864755,3	K562	blood:
14	chr10:49571375..49572211-chr10:49714319..49715238,7	MCF-7	breast:
15	chr10:49700642..49703834-chr10:49704395..49707390,3	K562	blood:
16	chr10:49655464..49657774-chr10:49727812..49730499,2	K562	blood:
17	chr10:49714562..49719396-chr10:49719920..49724610,6	K562	blood:
18	chr10:49516068..49518164-chr10:49716922..49719391,2	K562	blood:
19	chr10:49652128..49653347-chr10:49713187..49714230,4	MCF-7	breast:
20	chr10:49698967..49701120-chr10:49704411..49706305,2	K562	blood:
21	chr10:49729429..49732074-chr10:49751131..49754040,2	K562	blood:
22	chr10:49713648..49715470-chr10:49724741..49727947,3	K562	blood:
23	chr10:49579606..49581410-chr10:49715776..49718367,2	K562	blood:
24	chr10:49727015..49729249-chr10:49730487..49733103,2	MCF-7	breast:
25	chr10:49513508..49515174-chr10:49713887..49715575,2	K562	blood:
26	chr10:49714746..49717330-chr10:49717821..49719600,2	MCF-7	breast:
27	chr10:49561490..49563240-chr10:49725537..49727058,2	K562	blood:
28	chr10:49571889..49574086-chr10:49706276..49707792,2	K562	blood:
29	chr10:49723375..49726156-chr10:49734098..49735696,2	K562	blood:
30	chr10:49707073..49711100-chr10:49713490..49716250,3	K562	blood:
31	chr10:49698335..49701028-chr10:49818067..49819689,2	K562	blood:
32	chr10:49639661..49642619-chr10:49674798..49676427,2	K562	blood:
33	chr10:49718293..49721279-chr10:50504590..50507564,3	K562	blood:
34	chr10:49602827..49604920-chr10:49676681..49679745,3	K562	blood:
35	chr10:49660046..49662024-chr10:49725429..49726985,2	K562	blood:
36	chr10:49676784..49678693-chr10:49717036..49719541,2	K562	blood:
37	chr10:49731838..49732358-chr16:2014319..2015199,3	HCT-116	colon:
38	chr10:49728278..49730506-chr10:49735038..49737361,2	K562	blood:
39	chr10:49640741..49644596-chr10:49677175..49679458,3	K562	blood:
40	chr10:49423588..49424151-chr10:49714065..49715162,3	MCF-7	breast:
41	chr10:49686198..49686718-chr11:62608979..62609573,2	NB4	blood:
42	chr10:49692340..49695073-chr10:49708069..49710836,2	K562	blood:
43	chr10:49730645..49732196-chr10:49747881..49750168,2	K562	blood:
44	chr10:49714293..49714934-chr10:49863931..49864890,2	MCF-7	breast:
45	chr10:49701131..49703834-chr10:49704395..49706982,4	K562	blood:
46	chr10:49571219..49572252-chr10:49713441..49714210,3	MCF-7	breast:
47	chr10:49517657..49518610-chr10:49713350..49714126,2	MCF-7	breast:
48	chr10:49514209..49515853-chr10:49729935..49731994,2	K562	blood:
49	chr10:49659900..49662821-chr10:49704182..49706648,2	K562	blood:
50	chr10:49714827..49719872-chr10:49861427..49864767,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRMPD2-1	chr10:49719578-49719720	NONHSAT013274
2	lnc-FRMPD2-3	chr10:49676050-49677859	NONHSAT013272
3	lnc-FRMPD2-1	chr10:49718035-49718982	NONHSAT013274
4	lnc-FRMPD2-1	chr10:49717904-49719721	NONHSAT013273
5	lnc-FRMPD2-3	chr10:49687086-49687239	NONHSAT013272
6	lnc-FRMPD2-1	chr10:49719578-49719632	ENSG00000248682.1
7	lnc-FRMPD2-1	chr10:49718568-49718982	ENSG00000248682.1

No data

Variant related genes	Relation type
ARHGAP22-IT1	TF binding region
ARHGAP22	TF binding region
ARHGAP22-IT1	CpG island
ARHGAP22	CpG island
ENSG00000248682	chromatin interactions
ENSG00000107643	chromatin interactions
ENSG00000252577	chromatin interactions
ENSG00000140988	chromatin interactions
ENSG00000128805	chromatin interactions
ENSG00000177354	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000239653	chromatin interactions
ENSG00000236208	chromatin interactions
ENSG00000103043	chromatin interactions
ENSG00000255198	chromatin interactions

Extended variants
information (count: 2533 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:2533 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4838594	chr10:49669142-49669143	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs183722938	chr10:49669175-49669176	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs200010270	chr10:49669221-49669222	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs539166036	chr10:49669222-49669223	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs373441672	chr10:49669228-49669229	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs542201375	chr10:49669270-49669271	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs566507795	chr10:49669314-49669315	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs139511279	chr10:49669327-49669328	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs562113615	chr10:49669395-49669396	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575801245	chr10:49669397-49669398	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs186177242	chr10:49669450-49669451	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2034199	chr10:49669477-49669478	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs554848796	chr10:49669588-49669589	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573100161	chr10:49669652-49669653	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs558338938	chr10:49669669-49669670	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs145052071	chr10:49669710-49669711	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564285323	chr10:49669713-49669714	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs570188201	chr10:49669747-49669748	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs61838728	chr10:49669767-49669768	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs371658029	chr10:49669835-49669836	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs11814611	chr10:49669854-49669855	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190338468	chr10:49669988-49669989	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs367785248	chr10:49670026-49670027	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs575735761	chr10:49670090-49670091	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs546783031	chr10:49670111-49670112	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563504828	chr10:49670112-49670113	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs370546291	chr10:49670161-49670162	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs529195684	chr10:49670162-49670163	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs567940310	chr10:49670170-49670171	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs147553569	chr10:49670227-49670228	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs112266820	chr10:49670233-49670234	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs1867578	chr10:49670234-49670235	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs537523337	chr10:49670242-49670243	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149757439	chr10:49670272-49670273	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536441054	chr10:49670290-49670291	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs371262539	chr10:49670292-49670293	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs115811528	chr10:49670299-49670300	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs369169539	chr10:49670300-49670301	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs35916329	chr10:49670301-49670302	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs372552471	chr10:49670324-49670325	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573075390	chr10:49670366-49670367	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551159287	chr10:49670383-49670384	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs145613607	chr10:49670395-49670396	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs74130283	chr10:49670399-49670400	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs75077422	chr10:49670402-49670403	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs7914373	chr10:49670418-49670419	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs539607811	chr10:49670457-49670458	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562241383	chr10:49670469-49670470	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs574490097	chr10:49670487-49670488	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs148879007	chr10:49670492-49670493	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Schizophrenia	23813976	CNVD
Acute myeloid leukemia	19651601	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Rett syndrome	21593744	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	21948486	CNVD
cleft palate	21948486	CNVD
Encephalopathy	21948486	CNVD
Lung cancer	18438408	CNVD
T-cell primary immunodeficiency	21948486	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
speech delay	21948486	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1850 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49652000-49673000	Weak transcription	HMEC	breast
2	chr10:49653000-49673600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr10:49655200-49677800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr10:49657800-49677600	Weak transcription	HSMMtube	muscle
5	chr10:49661200-49669200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr10:49662200-49671800	Weak transcription	Aorta	Aorta
7	chr10:49662400-49672400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr10:49662600-49671800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr10:49664800-49669600	Weak transcription	Osteobl	bone
10	chr10:49664800-49671200	Weak transcription	Right Ventricle	heart
11	chr10:49664800-49671400	Weak transcription	Adipose Nuclei	Adipose
12	chr10:49664800-49671400	Weak transcription	NHDF-Ad	bronchial
13	chr10:49665200-49671600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr10:49665200-49673400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr10:49665400-49670800	Weak transcription	Ovary	ovary
16	chr10:49665400-49671200	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr10:49665400-49671200	Weak transcription	Brain Angular Gyrus	brain
18	chr10:49665400-49672200	Weak transcription	Spleen	Spleen
19	chr10:49665400-49675000	Weak transcription	HUVEC	blood vessel
20	chr10:49665800-49671200	Weak transcription	Brain Hippocampus Middle	brain
21	chr10:49665800-49671200	Weak transcription	Fetal Heart	heart
22	chr10:49665800-49671400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr10:49665800-49671400	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr10:49665800-49671600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr10:49665800-49672400	Weak transcription	Brain Substantia Nigra	brain
26	chr10:49666400-49671400	Weak transcription	Brain Cingulate Gyrus	brain
27	chr10:49666600-49671400	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr10:49667200-49671000	Weak transcription	Fetal Stomach	stomach
29	chr10:49667600-49670800	Strong transcription	HSMM	muscle
30	chr10:49668000-49669200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr10:49668200-49670600	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr10:49668200-49670800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr10:49668200-49671400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr10:49668200-49671400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr10:49668200-49674400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr10:49668400-49669200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr10:49668400-49669800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
38	chr10:49668400-49671000	Weak transcription	Primary hematopoietic stem cells	blood
39	chr10:49668400-49671800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr10:49668400-49676200	Weak transcription	NHLF	lung
41	chr10:49668600-49670800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr10:49668800-49673200	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr10:49668800-49674200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr10:49669000-49674000	Enhancers	K562	blood
45	chr10:49669200-49672000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr10:49669200-49674800	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr10:49669600-49670200	Strong transcription	Osteobl	bone
48	chr10:49669800-49672000	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr10:49670200-49675200	Weak transcription	Osteobl	bone
50	chr10:49670600-49673600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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