Variant report

Variant	esv3372246
Chromosome Location	chr11:71223101-71435819
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2855)
CpG islands
(count:6297)
Chromatin interactive
region (count:36)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2855 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:71291147-71291237	K562	blood:	n/a	n/a
2	ARID3A	chr11:71410234-71410262	K562	blood:	n/a	n/a
3	ARID3A	chr11:71417122-71417426	K562	blood:	n/a	n/a
4	ARID3A	chr11:71423994-71424313	K562	blood:	n/a	n/a
5	ARID3A	chr11:71416385-71416810	K562	blood:	n/a	n/a
6	ARID3A	chr11:71423449-71423649	K562	blood:	n/a	n/a
7	ARID3A	chr11:71237205-71237575	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:71246189-71246536	HepG2	liver:	n/a	n/a
9	ATF1	chr11:71430611-71430715	K562	blood:	n/a	n/a
10	ATF1	chr11:71417251-71417305	K562	blood:	n/a	n/a
11	ATF1	chr11:71274374-71274763	K562	blood:	n/a	n/a
12	ATF1	chr11:71328834-71328851	K562	blood:	n/a	n/a
13	ATF2	chr11:71262610-71263131	GM12878	blood:	n/a	n/a
14	ATF2	chr11:71251016-71252199	GM12878	blood:	n/a	n/a
15	ATF2	chr11:71254252-71254755	GM12878	blood:	n/a	n/a
16	ATF2	chr11:71251483-71252131	GM12878	blood:	n/a	n/a
17	ATF2	chr11:71251026-71251407	GM12878	blood:	n/a	n/a
18	ATF2	chr11:71254369-71254678	GM12878	blood:	n/a	n/a
19	ATF2	chr11:71241553-71242059	GM12878	blood:	n/a	n/a
20	ATF3	chr11:71390992-71391254	K562	blood:	n/a	n/a
21	ATF3	chr11:71300244-71300497	K562	blood:	n/a	n/a
22	ATF3	chr11:71416472-71416725	K562	blood:	n/a	n/a
23	BACH1	chr11:71291175-71291514	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr11:71262748-71263014	K562	blood:	n/a	n/a
25	BACH1	chr11:71262761-71263011	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr11:71421452-71421711	H1-hESC	embryonic stem cell:	n/a	n/a
27	BATF	chr11:71364018-71364247	GM12878	blood:	n/a	chr11:71364110-71364121
28	BATF	chr11:71262648-71263064	GM12878	blood:	n/a	chr11:71262880-71262891
29	BATF	chr11:71426864-71427152	GM12878	blood:	n/a	n/a
30	BATF	chr11:71407057-71407555	GM12878	blood:	n/a	n/a
31	BATF	chr11:71421930-71422331	GM12878	blood:	n/a	n/a
32	BATF	chr11:71300267-71300512	GM12878	blood:	n/a	n/a
33	BATF	chr11:71325819-71326075	GM12878	blood:	n/a	n/a
34	BATF	chr11:71315927-71316371	GM12878	blood:	n/a	n/a
35	BATF	chr11:71376144-71376697	GM12878	blood:	n/a	n/a
36	BATF	chr11:71398779-71399009	GM12878	blood:	n/a	n/a
37	BATF	chr11:71428726-71429101	GM12878	blood:	n/a	chr11:71428919-71428927
38	BATF	chr11:71364307-71364538	GM12878	blood:	n/a	n/a
39	BATF	chr11:71254310-71254769	GM12878	blood:	n/a	n/a
40	BATF	chr11:71426836-71427105	GM12878	blood:	n/a	n/a
41	BATF	chr11:71425014-71425933	GM12878	blood:	n/a	n/a
42	BATF	chr11:71254317-71254656	GM12878	blood:	n/a	n/a
43	BATF	chr11:71250991-71251419	GM12878	blood:	n/a	n/a
44	BATF	chr11:71376106-71376750	GM12878	blood:	n/a	n/a
45	BATF	chr11:71325884-71326044	GM12878	blood:	n/a	n/a
46	BATF	chr11:71428825-71429020	GM12878	blood:	n/a	chr11:71428919-71428927
47	BATF	chr11:71262740-71263045	GM12878	blood:	n/a	chr11:71262880-71262891
48	BATF	chr11:71425385-71425877	GM12878	blood:	n/a	n/a
49	BATF	chr11:71398772-71399069	GM12878	blood:	n/a	n/a
50	BATF	chr11:71251039-71251366	GM12878	blood:	n/a	n/a

(count:6297 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71276557-71276607	AG04449	skin:	fetal
2	chr11:71276654-71276704	ECC-1	luminal epithelium:	n/a
3	chr11:71230734-71230784	HL-60	blood:	n/a
4	chr11:71417713-71417763	SK-N-SH_RA	brain:	n/a
5	chr11:71311984-71312034	BJ	skin:	n/a
6	chr11:71230174-71230224	HPAEpiC	pulmonary alveolar:	n/a
7	chr11:71327353-71327403	HNPCEpiC	eye:	n/a
8	chr11:71248741-71248791	NHDF-neo	bronchial:	n/a
9	chr11:71294605-71294655	Hepatocyte	liver:	n/a
10	chr11:71294605-71294655	NT2-D1	testis:	n/a
11	chr11:71350346-71350396	BJ	skin:	n/a
12	chr11:71350888-71350938	GM06990	blood:	n/a
13	chr11:71293996-71294046	GM12891	blood:	n/a
14	chr11:71276654-71276704	HUVEC	blood vessel:	n/a
15	chr11:71276557-71276607	AG04449	skin:	fetal
16	chr11:71276654-71276704	ECC-1	luminal epithelium:	n/a
17	chr11:71230734-71230784	HL-60	blood:	n/a
18	chr11:71417713-71417763	SK-N-SH_RA	brain:	n/a
19	chr11:71311984-71312034	BJ	skin:	n/a
20	chr11:71230174-71230224	HPAEpiC	pulmonary alveolar:	n/a
21	chr11:71327353-71327403	HNPCEpiC	eye:	n/a
22	chr11:71248741-71248791	NHDF-neo	bronchial:	n/a
23	chr11:71294605-71294655	Hepatocyte	liver:	n/a
24	chr11:71294605-71294655	NT2-D1	testis:	n/a
25	chr11:71350346-71350396	BJ	skin:	n/a
26	chr11:71350888-71350938	GM06990	blood:	n/a
27	chr11:71293996-71294046	GM12891	blood:	n/a
28	chr11:71276654-71276704	HUVEC	blood vessel:	n/a
29	chr11:71418204-71418254	Hepatocyte	liver:	n/a
30	chr11:71285546-71285596	HRE	kidney:	n/a
31	chr11:71293892-71293942	A549	lung:	n/a
32	chr11:71421380-71421430	NHBE	bronchial:	n/a
33	chr11:71238382-71238432	SK-N-SH	brain:	n/a
34	chr11:71248741-71248791	GM12891	blood:	n/a
35	chr11:71320735-71320785	NB4	blood:	n/a
36	chr11:71259292-71259342	A549	lung:	n/a
37	chr11:71247746-71247796	HRCEpiC	kidney:	n/a
38	chr11:71340352-71340402	PFSK-1	brain:	n/a
39	chr11:71250073-71250123	BJ	skin:	n/a
40	chr11:71238205-71238255	H1-hESC	embryonic stem cell:	embryo
41	chr11:71295908-71295958	NB4	blood:	n/a
42	chr11:71287919-71287969	NHBE	bronchial:	n/a
43	chr11:71322699-71322749	HEK293	kidney:	embryo
44	chr11:71321132-71321182	GM12892	blood:	n/a
45	chr11:71340182-71340232	HL-60	blood:	n/a
46	chr11:71320513-71320563	HEEpiC	esophagus:	n/a
47	chr11:71237522-71237572	ovcar-3	ovarian:	n/a
48	chr11:71352122-71352172	Jurkat	blood:	n/a
49	chr11:71294744-71294794	AG09319	gingival:	n/a
50	chr11:71295678-71295728	SK-N-MC	brain:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:71272055..71274887-chr11:71280546..71282110,2	K562	blood:
2	chr11:71278406..71279386-chr11:71291430..71292089,2	MCF-7	breast:
3	chr11:71282448..71285837-chr11:71286010..71289392,3	MCF-7	breast:
4	chr11:71176264..71179140-chr11:71273245..71275842,2	MCF-7	breast:
5	chr11:71253515..71257343-chr11:71260479..71262893,3	MCF-7	breast:
6	chr11:71279845..71280406-chr11:71290008..71290749,2	MCF-7	breast:
7	chr11:71185954..71187783-chr11:71290414..71293087,2	MCF-7	breast:
8	chr11:71279425..71280036-chr11:71290519..71291383,2	MCF-7	breast:
9	chr11:71158649..71161220-chr11:71291218..71293129,2	MCF-7	breast:
10	chr11:71278628..71280477-chr11:71289049..71291000,2	MCF-7	breast:
11	chr11:71221136..71223101-chr11:71257935..71260917,2	MCF-7	breast:
12	chr11:71198072..71200599-chr11:71283906..71285709,2	MCF-7	breast:
13	chr11:71278406..71279386-chr11:71291430..71292089,2	MCF-7	breast:
14	chr11:71282448..71285837-chr11:71286010..71289392,3	MCF-7	breast:
15	chr11:71254168..71255682-chr11:71257713..71259935,2	MCF-7	breast:
16	chr11:71230161..71233081-chr11:71237007..71238796,2	MCF-7	breast:
17	chr11:71272055..71274887-chr11:71280546..71282110,2	K562	blood:
18	chr11:71163473..71165824-chr11:71289975..71292795,2	MCF-7	breast:
19	chr11:71253515..71257343-chr11:71260479..71262893,3	MCF-7	breast:
20	chr11:71349980..71350709-chr11:71511135..71512071,2	K562	blood:
21	chr11:71257442..71259140-chr11:71259571..71262525,2	K562	blood:
22	chr11:71198148..71200436-chr11:71273726..71275977,2	MCF-7	breast:
23	chr11:71279845..71280406-chr11:71290008..71290749,2	MCF-7	breast:
24	chr11:71189071..71191550-chr11:71272066..71273804,2	MCF-7	breast:
25	chr11:71284028..71285602-chr11:71289697..71292475,2	MCF-7	breast:
26	chr11:71257442..71259140-chr11:71259571..71262525,2	K562	blood:
27	chr11:71156732..71161621-chr11:71272936..71276184,4	MCF-7	breast:
28	chr11:71278628..71280477-chr11:71289049..71291000,2	MCF-7	breast:
29	chr11:71209230..71212129-chr11:71251545..71253303,2	MCF-7	breast:
30	chr11:71162651..71164294-chr11:71282060..71284159,2	K562	blood:
31	chr11:71158604..71160379-chr11:71280505..71283180,2	MCF-7	breast:
32	chr11:71290639..71292875-chr11:71296370..71298788,2	MCF-7	breast:
33	chr11:71192889..71195578-chr11:71229380..71232124,2	MCF-7	breast:
34	chr11:71159116..71165503-chr11:71274687..71279227,9	MCF-7	breast:
35	chr11:71278394..71279845-chr11:71290961..71292008,7	MCF-7	breast:
36	chr11:71279425..71280036-chr11:71290519..71291383,2	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP000867.1-2	chr11:71383721-71384047	ENSG00000254504.1
2	lnc-FAM86C1-4	chr11:71393417-71393825	expRegAs_chr11_7370_+
3	lnc-AP000867.1-2	chr11:71421533-71421627	ENSG00000254504.1
4	lnc-AP000867.1-3	chr11:71292956-71293203	NONHSAT022693
5	lnc-KRTAP5-10-1	chr11:71279726-71279980	NONHSAT022692
6	lnc-FAM86C1-1	chr11:71433219-71433273	NONHSAT022701
7	lnc-FAM86C1-5	chr11:71392883-71393202	expRegAs_chr11_7367_+
8	lnc-AP000867.1-3	chr11:71310043-71310371	NONHSAT022693
9	lnc-AP000867.1-1	chr11:71415223-71415306	ENSG00000254972
10	lnc-FAM86C1-1	chr11:71422786-71422863	NONHSAT022701
11	lnc-FAM86C1-1	chr11:71425421-71425604	NONHSAT022701
12	lnc-AP000867.1-1	chr11:71416406-71416450	ENSG00000254972
13	lnc-AP000867.1-4	chr11:71401499-71401703	NONHSAT022697
14	lnc-FAM86C1-3	chr11:71394183-71394998	expRegAs_chr11_7373_+
15	lnc-FAM86C1-2	chr11:71395710-71396117	expRegAs_chr11_7374_+
16	lnc-AP000867.1-1	chr11:71412314-71412531	ENSG00000254972
17	lnc-AP000867.1-3	chr11:71314349-71314399	NONHSAT022693

No data

Variant related genes	Relation type
OR7E87P	TF binding region
KRTAP5-10	TF binding region
OR7E4P	TF binding region
KRTAP5-9	TF binding region
ENSG00000254805	TF binding region
ENSG00000248903	TF binding region
ENPP7P8	TF binding region
ENSG00000221458	TF binding region
ENSG00000255415	TF binding region
KRTAP5-7	TF binding region
ENSG00000223235	TF binding region
ENSG00000254972	TF binding region
KRTAP5-14P	TF binding region
ENSG00000187811	TF binding region
KRTAP5-11	TF binding region
KRTAP5-8	TF binding region
UNC93B6	TF binding region
RPS3AP41	TF binding region
OR7E87P	CpG island
KRTAP5-10	CpG island
OR7E4P	CpG island
KRTAP5-9	CpG island
ENSG00000254805	CpG island
ENSG00000248903	CpG island
ENPP7P8	CpG island
ENSG00000221458	CpG island
ENSG00000255415	CpG island
KRTAP5-7	CpG island
ENSG00000223235	CpG island
ENSG00000254972	CpG island
KRTAP5-14P	CpG island
ENSG00000187811	CpG island
KRTAP5-11	CpG island
KRTAP5-8	CpG island
UNC93B6	CpG island
RPS3AP41	CpG island
ENSG00000172890	chromatin interactions
ENSG00000244411	chromatin interactions
ENSG00000249387	chromatin interactions
ENSG00000248903	chromatin interactions
ENSG00000254682	chromatin interactions
ENSG00000254997	chromatin interactions
ENSG00000172893	chromatin interactions

Extended variants
information (count: 10654 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:10654 , 50 per page) page: 1 2 3 4 5 6 7 ... 214

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148695352	chr11:71223114-71223115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs551579535	chr11:71223144-71223145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570070672	chr11:71223148-71223149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144360510	chr11:71223160-71223161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs549350363	chr11:71223161-71223162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559100619	chr11:71223178-71223179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs193143649	chr11:71223234-71223235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535300559	chr11:71223252-71223253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs79326857	chr11:71223256-71223257	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
10	rs571726348	chr11:71223294-71223295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs199707220	chr11:71223302-71223303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538775179	chr11:71223372-71223373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556771949	chr11:71223377-71223378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs146615255	chr11:71223413-71223414	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
15	rs542220085	chr11:71223418-71223419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs376187734	chr11:71223445-71223446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189001837	chr11:71223511-71223512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553366385	chr11:71223529-71223530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571677801	chr11:71223530-71223531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs572820036	chr11:71223566-71223567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371394178	chr11:71223588-71223589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540132837	chr11:71223599-71223600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376192749	chr11:71223613-71223614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565131646	chr11:71223614-71223615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532196762	chr11:71223625-71223626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs377747886	chr11:71223656-71223657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370921499	chr11:71223695-71223696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375825991	chr11:71223707-71223708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544351955	chr11:71223721-71223722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs142532522	chr11:71223738-71223739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530997331	chr11:71223796-71223797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs184041885	chr11:71223816-71223817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567648063	chr11:71223868-71223869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528822760	chr11:71223874-71223875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188785494	chr11:71223907-71223908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148838851	chr11:71224042-71224043	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
37	rs576283627	chr11:71224093-71224094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs538869508	chr11:71224132-71224133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139546838	chr11:71224145-71224146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568636604	chr11:71224166-71224167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186935803	chr11:71224170-71224171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145178616	chr11:71224173-71224174	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
43	rs372140171	chr11:71224243-71224244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572498925	chr11:71224269-71224270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540559367	chr11:71224328-71224329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558582377	chr11:71224371-71224372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376719554	chr11:71224404-71224405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs147961448	chr11:71224407-71224408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577020459	chr11:71224410-71224411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544097216	chr11:71224453-71224454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:1006 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71211800-71232400	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr11:71213200-71232200	Weak transcription	Brain Angular Gyrus	brain
3	chr11:71215600-71236600	Weak transcription	Brain Anterior Caudate	brain
4	chr11:71216400-71235400	Weak transcription	Brain Substantia Nigra	brain
5	chr11:71222000-71230400	Weak transcription	HSMMtube	muscle
6	chr11:71228000-71232200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr11:71229400-71229600	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr11:71229600-71232200	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr11:71230000-71230800	Enhancers	Placenta	Placenta
10	chr11:71230000-71232200	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr11:71230200-71231600	Enhancers	Fetal Muscle Leg	muscle
12	chr11:71230400-71231400	Enhancers	Fetal Muscle Trunk	muscle
13	chr11:71230400-71231400	Enhancers	HSMM	muscle
14	chr11:71230400-71231400	Enhancers	HSMMtube	muscle
15	chr11:71230400-71232200	Weak transcription	Brain Cingulate Gyrus	brain
16	chr11:71230400-71235800	Weak transcription	Brain Hippocampus Middle	brain
17	chr11:71230800-71233600	Weak transcription	Adipose Nuclei	Adipose
18	chr11:71232200-71232800	Strong transcription	Brain Angular Gyrus	brain
19	chr11:71232200-71232800	Strong transcription	Brain Cingulate Gyrus	brain
20	chr11:71232200-71232800	Strong transcription	Brain Inferior Temporal Lobe	brain
21	chr11:71232200-71232800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr11:71232200-71233000	Strong transcription	Skeletal Muscle Male	skeletal muscle
23	chr11:71232400-71232800	ZNF genes & repeats	Pancreas	Pancrea
24	chr11:71232400-71232800	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
25	chr11:71232800-71233200	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr11:71232800-71236400	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr11:71232800-71236600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr11:71232800-71243600	Weak transcription	Brain Angular Gyrus	brain
29	chr11:71232800-71245800	Weak transcription	Pancreas	Pancrea
30	chr11:71232800-71259800	Weak transcription	Brain Cingulate Gyrus	brain
31	chr11:71233000-71235600	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr11:71235800-71238000	Enhancers	HepG2	liver
33	chr11:71236200-71239200	Enhancers	Liver	Liver
34	chr11:71236400-71237800	Enhancers	A549	lung
35	chr11:71236600-71236800	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
36	chr11:71236600-71237400	Enhancers	Stomach Mucosa	stomach
37	chr11:71236800-71237000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr11:71237200-71238800	Enhancers	Fetal Intestine Large	intestine
39	chr11:71237400-71238200	Enhancers	Fetal Intestine Small	intestine
40	chr11:71238000-71238200	Flanking Active TSS	HepG2	liver
41	chr11:71238200-71238600	Active TSS	HepG2	liver
42	chr11:71238600-71239000	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr11:71238600-71239000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr11:71238600-71239000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
45	chr11:71238600-71239200	Flanking Active TSS	HepG2	liver
46	chr11:71239000-71241400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr11:71239000-71246400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr11:71239200-71239800	Enhancers	HepG2	liver
49	chr11:71239800-71241600	Weak transcription	HepG2	liver
50	chr11:71241400-71242600	Enhancers	GM12878-XiMat	blood

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