Variant report

Variant	nsv832119
Chromosome Location	chr11:34815528-35009370
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3058)
CpG islands
(count:1894)
Chromatin interactive
region (count:182)
LncRNA
region (count:6)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:3058 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:34838367-34838413	K562	blood:	n/a	n/a
2	ARID3A	chr11:34830689-34831538	K562	blood:	n/a	n/a
3	ARID3A	chr11:34912499-34912747	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:34938026-34938300	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:34947622-34948038	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:34874465-34874468	K562	blood:	n/a	n/a
7	ARID3A	chr11:34951031-34952265	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:34847583-34848216	K562	blood:	n/a	n/a
9	ARID3A	chr11:34949977-34949978	K562	blood:	n/a	n/a
10	ARID3A	chr11:34831953-34831998	K562	blood:	n/a	n/a
11	ARID3A	chr11:34947668-34948079	K562	blood:	n/a	n/a
12	ARID3A	chr11:34911682-34911835	HepG2	liver:	n/a	n/a
13	ARID3A	chr11:34912409-34912729	K562	blood:	n/a	n/a
14	ARID3A	chr11:34937595-34937654	HepG2	liver:	n/a	n/a
15	ARID3A	chr11:34847164-34847909	HepG2	liver:	n/a	n/a
16	ARID3A	chr11:34827457-34827921	K562	blood:	n/a	n/a
17	ARID3A	chr11:34828529-34828710	K562	blood:	n/a	n/a
18	ATF1	chr11:34893244-34893280	K562	blood:	n/a	n/a
19	ATF1	chr11:34868139-34868315	K562	blood:	n/a	n/a
20	ATF1	chr11:34938972-34939307	K562	blood:	n/a	n/a
21	ATF1	chr11:34871920-34872197	K562	blood:	n/a	n/a
22	ATF1	chr11:34875490-34875687	K562	blood:	n/a	n/a
23	ATF1	chr11:34885484-34885496	K562	blood:	n/a	n/a
24	ATF1	chr11:34851600-34851979	K562	blood:	n/a	n/a
25	ATF1	chr11:34831188-34831517	K562	blood:	n/a	n/a
26	ATF1	chr11:34841693-34841966	K562	blood:	n/a	n/a
27	ATF1	chr11:34827473-34827813	K562	blood:	n/a	n/a
28	ATF1	chr11:34961726-34961907	K562	blood:	n/a	n/a
29	ATF1	chr11:34847507-34847873	K562	blood:	n/a	n/a
30	ATF2	chr11:34937331-34938461	GM12878	blood:	n/a	n/a
31	ATF2	chr11:34842422-34842939	GM12878	blood:	n/a	n/a
32	ATF3	chr11:34937943-34938123	K562	blood:	n/a	chr11:34938069-34938078
33	ATF3	chr11:34929799-34930110	K562	blood:	n/a	n/a
34	ATF3	chr11:34830633-34831620	K562	blood:	n/a	n/a
35	BACH1	chr11:34816276-34816610	K562	blood:	n/a	n/a
36	BACH1	chr11:34929538-34930075	H1-hESC	embryonic stem cell:	n/a	chr11:34929943-34929957
37	BACH1	chr11:34816262-34816669	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr11:34817624-34817766	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr11:34929700-34929782	K562	blood:	n/a	n/a
40	BATF	chr11:34929853-34930086	GM12878	blood:	n/a	chr11:34929946-34929957
41	BATF	chr11:34842574-34842804	GM12878	blood:	n/a	n/a
42	BATF	chr11:34842550-34842835	GM12878	blood:	n/a	n/a
43	BCL3	chr11:34937631-34938491	A549	lung:	n/a	chr11:34937662-34937675 chr11:34937706-34937719 chr11:34938167-34938180 chr11:34938070-34938079
44	BCLAF1	chr11:34937505-34938414	GM12878	blood:	n/a	chr11:34937662-34937675 chr11:34937706-34937719 chr11:34938167-34938180 chr11:34938070-34938079
45	BCLAF1	chr11:34842490-34842936	GM12878	blood:	n/a	n/a
46	BHLHE40	chr11:34951357-34951887	HepG2	liver:	n/a	n/a
47	BHLHE40	chr11:34908226-34908557	HepG2	liver:	n/a	n/a
48	BHLHE40	chr11:34951426-34951824	HepG2	liver:	n/a	n/a
49	BHLHE40	chr11:34859156-34859342	HepG2	liver:	n/a	n/a
50	BHLHE40	chr11:34828445-34828785	K562	blood:	n/a	chr11:34828586-34828599

(count:1894 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:34881685-34881735	BE2_C	brain:	n/a
2	chr11:34876740-34876790	HepG2	liver:	n/a
3	chr11:34937484-34937534	GM19239	blood:	n/a
4	chr11:34881685-34881735	BE2_C	brain:	n/a
5	chr11:34876740-34876790	HepG2	liver:	n/a
6	chr11:34937484-34937534	GM19239	blood:	n/a
7	chr11:34934680-34934730	AG09319	gingival:	n/a
8	chr11:34936781-34936831	NB4	blood:	n/a
9	chr11:34938014-34938064	BJ	skin:	n/a
10	chr11:34847603-34847653	Jurkat	blood:	n/a
11	chr11:34936862-34936912	MCF10A-Er-Src	breast:	n/a
12	chr11:34937564-34937614	NHDF-neo	bronchial:	n/a
13	chr11:34937341-34937391	BE2_C	brain:	n/a
14	chr11:34881685-34881735	HAEpiC	amniotic membrane:	n/a
15	chr11:34938014-34938064	GM12891	blood:	n/a
16	chr11:34937665-34937715	HEK293	kidney:	embryo
17	chr11:34940794-34940844	U87	brain:	n/a
18	chr11:34940794-34940844	AG09319	gingival:	n/a
19	chr11:34937647-34937697	NHDF-neo	bronchial:	n/a
20	chr11:34929792-34929842	SKMC	muscle:	n/a
21	chr11:34937341-34937391	AoSMC	blood vessel:	n/a
22	chr11:34936781-34936831	A549	lung:	n/a
23	chr11:34937564-34937614	HUVEC	blood vessel:	n/a
24	chr11:34951024-34951074	BE2_C	brain:	n/a
25	chr11:34938234-34938284	GM06990	blood:	n/a
26	chr11:34858035-34858085	Caco-2	colon:	n/a
27	chr11:34937559-34937609	T-47D	breast:	n/a
28	chr11:34938143-34938193	BJ	skin:	n/a
29	chr11:34949324-34949374	HRCEpiC	kidney:	n/a
30	chr11:34876740-34876790	HEK293	kidney:	embryo
31	chr11:34938234-34938284	ovcar-3	ovarian:	n/a
32	chr11:34937559-34937609	HepG2	liver:	n/a
33	chr11:34881685-34881735	HCM	heart:	n/a
34	chr11:34936781-34936831	LNCaP	prostate:	n/a
35	chr11:34936781-34936831	HCM	heart:	n/a
36	chr11:34937992-34938042	GM06990	blood:	n/a
37	chr11:34937665-34937715	Jurkat	blood:	n/a
38	chr11:34881685-34881735	GM12878	blood:	n/a
39	chr11:34938507-34938557	MCF-7	breast:	n/a
40	chr11:34940794-34940844	NH-A	brain:	n/a
41	chr11:34937992-34938042	HCT-116	colon:	n/a
42	chr11:34938507-34938557	ProgFib	skin:	n/a
43	chr11:34937933-34937983	HCM	heart:	n/a
44	chr11:34937958-34938008	AG04449	skin:	fetal
45	chr11:34937992-34938042	SK-N-SH	brain:	n/a
46	chr11:34937484-34937534	BJ	skin:	n/a
47	chr11:34937573-34937623	A549	lung:	n/a
48	chr11:34945827-34945877	GM19239	blood:	n/a
49	chr11:34938507-34938557	HL-60	blood:	n/a
50	chr11:34938348-34938398	HCF	heart:	n/a

(count:182 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr11:34928718..34934554-chr11:34935181..34939232,15	MCF-7	breast:
2	chr11:34905872..34908385-chr11:34915875..34918496,2	K562	blood:
3	chr11:34938030..34938538-chr11:82996860..82997460,2	Hela-S3	cervix:
4	chr11:34947747..34948295-chr11:35506935..35507466,2	K562	blood:
5	chr11:34830057..34832042-chr11:34848126..34850634,2	K562	blood:
6	chr11:34846502..34848843-chr11:34871445..34873663,2	K562	blood:
7	chr11:34686698..34687242-chr11:34844773..34845279,2	MCF-7	breast:
8	chr11:34956035..34958785-chr11:35004705..35006336,2	MCF-7	breast:
9	chr11:34828810..34832933-chr11:34843194..34845330,4	K562	blood:
10	chr11:34870702..34872577-chr11:34878120..34880872,2	K562	blood:
11	chr11:34923966..34926335-chr11:34931824..34933676,2	K562	blood:
12	chr11:34631109..34633523-chr11:34830130..34832941,2	K562	blood:
13	chr11:34827577..34829280-chr11:34846794..34848443,2	K562	blood:
14	chr11:34919773..34921558-chr11:34929230..34931688,2	K562	blood:
15	chr11:34775760..34778139-chr11:34861633..34864027,2	K562	blood:
16	chr11:34989938..34992204-chr11:35000945..35002458,2	K562	blood:
17	chr11:34534104..34535140-chr11:34920268..34920796,4	K562	blood:
18	chr11:34947697..34948269-chr11:35163627..35164578,3	K562	blood:
19	chr11:34960896..34963192-chr11:34963561..34965150,2	K562	blood:
20	chr11:34868671..34870522-chr11:34876282..34878999,2	MCF-7	breast:
21	chr11:34891295..34892870-chr11:34893606..34896164,2	K562	blood:
22	chr11:34890239..34892870-chr11:34894138..34896164,2	K562	blood:
23	chr11:34947799..34948300-chr11:35326589..35327576,2	K562	blood:
24	chr11:34865938..34868708-chr11:34870452..34873276,2	K562	blood:
25	chr11:34591227..34593757-chr11:34936738..34938685,2	MCF-7	breast:
26	chr11:34938207..34939863-chr11:35260000..35262264,2	K562	blood:
27	chr11:34831422..34835034-chr11:34838233..34841793,4	K562	blood:
28	chr11:34954386..34956581-chr11:34957357..34959864,2	MCF-7	breast:
29	chr11:34846388..34848890-chr11:34858178..34860592,2	MCF-7	breast:
30	chr11:34937866..34938405-chr16:87425618..87426289,2	HCT-116	colon:
31	chr11:34840398..34841965-chr11:34845264..34846905,2	K562	blood:
32	chr11:34875503..34877981-chr11:34878649..34881731,3	K562	blood:
33	chr11:34863977..34866462-chr11:34870377..34873238,2	MCF-7	breast:
34	chr11:34865938..34868708-chr11:34870452..34873276,2	K562	blood:
35	chr11:34936821..34938525-chr17:38476825..38479359,2	MCF-7	breast:
36	chr11:34936076..34941004-chr11:34952159..34955870,7	K562	blood:
37	chr11:34768738..34771170-chr11:34853652..34856105,2	K562	blood:
38	chr11:34944920..34946901-chr11:34953844..34956335,2	K562	blood:
39	chr11:34937322..34938942-chr11:35639938..35642002,2	MCF-7	breast:
40	chr11:34954216..34955992-chr11:34958074..34960760,2	MCF-7	breast:
41	chr11:34944920..34946901-chr11:34953844..34956335,2	K562	blood:
42	chr11:34831422..34835034-chr11:34838233..34841793,4	K562	blood:
43	chr11:34868671..34870522-chr11:34876282..34878999,2	MCF-7	breast:
44	chr11:34937272..34938502-chr11:118134559..118135201,3	Hela-S3	cervix:
45	chr11:34937811..34940525-chr11:34962659..34964952,2	MCF-7	breast:
46	chr11:34954216..34955992-chr11:34958074..34960760,2	MCF-7	breast:
47	chr11:34921303..34922935-chr11:34924601..34927346,2	MCF-7	breast:
48	chr11:34891295..34892870-chr11:34893606..34896164,2	K562	blood:
49	chr11:34899153..34900913-chr11:34902618..34905230,2	K562	blood:
50	chr11:34878119..34880348-chr11:34884856..34886591,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ELF5-3	chr11:34880399-34880602	XLOC_009414
2	lnc-ELF5-3	chr11:34843144-34843177	NONHSAT018762
3	lnc-ELF5-3	chr11:34843184-34843319	NONHSAT018762
4	lnc-ELF5-3	chr11:34877836-34878189	NONHSAT018762
5	lnc-ELF5-3	chr11:34876859-34878189	XLOC_009414
6	lnc-ELF5-3	chr11:34876500-34876870	NONHSAT018762

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1343-5p	chr11:34963398-34963419	MIMAT0027038
hsa-miR-1343-3p	chr11:34963435-34963456	MIMAT0019776

No data

Variant related genes	Relation type
MIR1343	TF binding region
PDHX	TF binding region
APIP	TF binding region
MIR1343	CpG island
PDHX	CpG island
APIP	CpG island
ENSG00000131759	chromatin interactions
ENSG00000137500	chromatin interactions
ENSG00000251862	chromatin interactions
ENSG00000149573	chromatin interactions
ENSG00000110435	chromatin interactions
ENSG00000228649	chromatin interactions
ENSG00000179431	chromatin interactions
ENSG00000149089	chromatin interactions
ENSG00000140941	chromatin interactions
ENSG00000255234	chromatin interactions
ENSG00000099860	chromatin interactions
ENSG00000103264	chromatin interactions
ENSG00000255427	chromatin interactions

Extended variants
information (count: 7620 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:7620 , 50 per page) page: 1 2 3 4 5 6 7 ... 153

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375178853	chr11:34815537-34815538	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs367681292	chr11:34815572-34815573	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs572623465	chr11:34815640-34815641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs374823984	chr11:34815680-34815681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541754195	chr11:34815690-34815691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs371929089	chr11:34815704-34815705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs72920723	chr11:34815711-34815712	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs543776745	chr11:34815766-34815767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563673585	chr11:34815779-34815780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs532636182	chr11:34815790-34815791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs143794776	chr11:34815849-34815850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11032878	chr11:34815886-34815887	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs183915674	chr11:34815941-34815942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189374540	chr11:34816020-34816021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs12363271	chr11:34816046-34816047	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs567204000	chr11:34816047-34816048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs7130756	chr11:34816058-34816059	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs549738342	chr11:34816075-34816076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs569694054	chr11:34816076-34816077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs148170523	chr11:34816097-34816098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs558642664	chr11:34816098-34816099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs555210890	chr11:34816101-34816102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs836457	chr11:34816131-34816132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535202341	chr11:34816160-34816161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs113587163	chr11:34816207-34816208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs555328835	chr11:34816215-34816216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs145948735	chr11:34816219-34816220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs74896017	chr11:34816221-34816222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565660386	chr11:34816268-34816269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182583026	chr11:34816273-34816274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs546295935	chr11:34816312-34816313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139858373	chr11:34816325-34816326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs186700079	chr11:34816335-34816336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191655388	chr11:34816358-34816359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181816572	chr11:34816359-34816360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs552651157	chr11:34816379-34816380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs12287607	chr11:34816380-34816381	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs1858168	chr11:34816449-34816450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs577707723	chr11:34816480-34816481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs569641192	chr11:34816516-34816517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs75145230	chr11:34816523-34816524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs1858167	chr11:34816531-34816532	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs558099753	chr11:34816615-34816616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs114395926	chr11:34816618-34816619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs113669301	chr11:34816622-34816623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs58907934	chr11:34816653-34816654	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs535266772	chr11:34816668-34816669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs185340875	chr11:34816683-34816684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs568514237	chr11:34816697-34816698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576554453	chr11:34816698-34816699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:3830 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34811400-34816000	Weak transcription	Esophagus	oesophagus
2	chr11:34811800-34818800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:34812800-34815600	Enhancers	Brain Substantia Nigra	brain
4	chr11:34812800-34817800	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr11:34813200-34815600	Enhancers	Brain Anterior Caudate	brain
6	chr11:34813200-34815600	Enhancers	Brain Cingulate Gyrus	brain
7	chr11:34813200-34815600	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr11:34813800-34818000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr11:34814000-34815600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr11:34814000-34815600	Enhancers	Brain Angular Gyrus	brain
11	chr11:34814200-34815600	Enhancers	Fetal Lung	lung
12	chr11:34814200-34820400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr11:34814600-34816000	Weak transcription	Right Atrium	heart
14	chr11:34814600-34816600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr11:34814600-34817600	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr11:34814800-34817000	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr11:34814800-34817200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr11:34815000-34816000	Enhancers	Adipose Nuclei	Adipose
19	chr11:34815000-34816200	Weak transcription	Stomach Mucosa	stomach
20	chr11:34815000-34817600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr11:34815000-34821200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr11:34815000-34833600	Weak transcription	HepG2	liver
23	chr11:34815200-34815800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr11:34815400-34815600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr11:34815400-34815600	Enhancers	Pancreas	Pancrea
26	chr11:34816000-34816200	Enhancers	Esophagus	oesophagus
27	chr11:34816000-34816200	Enhancers	Right Atrium	heart
28	chr11:34816600-34816800	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr11:34816800-34817200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr11:34817000-34817800	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr11:34817200-34817400	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr11:34817200-34817800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr11:34817200-34817800	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr11:34817400-34817600	Enhancers	H1 Cell Line	embryonic stem cell
35	chr11:34817400-34817600	Enhancers	H9 Cell Line	embryonic stem cell
36	chr11:34817400-34817800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr11:34817600-34819000	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr11:34817600-34819800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr11:34817600-34819800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
40	chr11:34817800-34818400	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr11:34819000-34819200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
42	chr11:34819000-34819400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr11:34819000-34819600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr11:34819400-34820600	Weak transcription	Stomach Mucosa	stomach
45	chr11:34819600-34821800	Enhancers	Liver	Liver
46	chr11:34819800-34827000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr11:34820200-34820800	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr11:34820600-34821400	Enhancers	Stomach Mucosa	stomach
49	chr11:34820800-34822600	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr11:34822600-34823000	Enhancers	Pancreatic Islets	Pancreatic Islet

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