Variant report

Variant	nsv482905
Chromosome Location	chr11:17170690-17320691
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2711)
CpG islands
(count:2197)
Chromatin interactive
region (count:144)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2711 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:17230806-17231140	K562	blood:	n/a	n/a
2	ARID3A	chr11:17229421-17229621	K562	blood:	n/a	n/a
3	ARID3A	chr11:17208257-17209406	K562	blood:	n/a	n/a
4	ARID3A	chr11:17278920-17279163	K562	blood:	n/a	n/a
5	ARID3A	chr11:17243679-17243693	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:17297923-17298398	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:17297898-17298099	K562	blood:	n/a	n/a
8	ARID3A	chr11:17280101-17280301	HepG2	liver:	n/a	n/a
9	ARID3A	chr11:17229393-17231090	HepG2	liver:	n/a	n/a
10	ARID3A	chr11:17296980-17297198	HepG2	liver:	n/a	n/a
11	ARID3A	chr11:17279960-17280656	K562	blood:	n/a	n/a
12	ARID3A	chr11:17285424-17285657	K562	blood:	n/a	n/a
13	ARID3A	chr11:17298792-17299541	K562	blood:	n/a	n/a
14	ARID3A	chr11:17298969-17299169	HepG2	liver:	n/a	n/a
15	ARID3A	chr11:17218950-17219634	HepG2	liver:	n/a	n/a
16	ATF1	chr11:17208539-17208866	K562	blood:	n/a	n/a
17	ATF1	chr11:17278815-17279151	K562	blood:	n/a	n/a
18	ATF1	chr11:17229335-17229716	K562	blood:	n/a	n/a
19	ATF1	chr11:17290015-17290215	K562	blood:	n/a	n/a
20	ATF1	chr11:17241708-17241757	K562	blood:	n/a	n/a
21	ATF1	chr11:17281533-17282229	K562	blood:	n/a	n/a
22	ATF1	chr11:17201255-17201359	K562	blood:	n/a	n/a
23	ATF1	chr11:17280253-17280551	K562	blood:	n/a	n/a
24	ATF2	chr11:17265520-17265987	GM12878	blood:	n/a	n/a
25	ATF2	chr11:17265570-17265940	GM12878	blood:	n/a	n/a
26	ATF2	chr11:17252887-17253312	GM12878	blood:	n/a	n/a
27	ATF2	chr11:17252355-17252821	GM12878	blood:	n/a	n/a
28	ATF2	chr11:17229242-17229795	GM12878	blood:	n/a	n/a
29	ATF2	chr11:17252958-17253367	GM12878	blood:	n/a	n/a
30	ATF2	chr11:17252297-17252878	GM12878	blood:	n/a	n/a
31	ATF2	chr11:17229816-17230323	GM12878	blood:	n/a	chr11:17230300-17230307
32	ATF2	chr11:17175863-17176292	GM12878	blood:	n/a	n/a
33	ATF2	chr11:17229840-17230305	H1-hESC	embryonic stem cell:	n/a	n/a
34	ATF2	chr11:17315464-17316124	GM12878	blood:	n/a	n/a
35	ATF2	chr11:17229351-17229789	H1-hESC	embryonic stem cell:	n/a	n/a
36	ATF2	chr11:17229679-17230227	H1-hESC	embryonic stem cell:	n/a	n/a
37	ATF2	chr11:17297511-17298222	GM12878	blood:	n/a	n/a
38	ATF2	chr11:17319739-17320323	GM12878	blood:	n/a	n/a
39	ATF2	chr11:17319713-17320319	GM12878	blood:	n/a	n/a
40	ATF2	chr11:17315495-17315916	GM12878	blood:	n/a	n/a
41	ATF3	chr11:17229880-17230169	K562	blood:	n/a	n/a
42	ATF3	chr11:17285406-17285659	K562	blood:	n/a	n/a
43	ATF3	chr11:17229841-17230201	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr11:17298260-17298283	K562	blood:	n/a	n/a
45	BACH1	chr11:17239132-17239269	K562	blood:	n/a	n/a
46	BACH1	chr11:17297732-17298136	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr11:17174185-17174187	K562	blood:	n/a	n/a
48	BACH1	chr11:17229738-17229886	K562	blood:	n/a	n/a
49	BATF	chr11:17315531-17315975	GM12878	blood:	n/a	n/a
50	BATF	chr11:17176430-17176573	GM12878	blood:	n/a	n/a

(count:2197 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:17300909-17300959	Hela-S3	cervix:	n/a
2	chr11:17300909-17300959	Hela-S3	cervix:	n/a
3	chr11:17249967-17250017	MCF-7	breast:	n/a
4	chr11:17298266-17298316	HEEpiC	esophagus:	n/a
5	chr11:17297984-17298034	AG09319	gingival:	n/a
6	chr11:17298268-17298318	NB4	blood:	n/a
7	chr11:17249958-17250008	HCPEpiC	choroid plexus:	n/a
8	chr11:17191617-17191667	SK-N-MC	brain:	n/a
9	chr11:17192372-17192422	SAEC	small airway:	n/a
10	chr11:17298273-17298323	RPTEC	kidney:	n/a
11	chr11:17298537-17298587	HEK293	kidney:	embryo
12	chr11:17300909-17300959	SK-N-MC	brain:	n/a
13	chr11:17226015-17226065	AG04449	skin:	fetal
14	chr11:17232377-17232427	PANC-1	pancreas:	n/a
15	chr11:17298266-17298316	GM06990	blood:	n/a
16	chr11:17298064-17298114	SK-N-SH	brain:	n/a
17	chr11:17248467-17248517	Hela-S3	cervix:	n/a
18	chr11:17226015-17226065	PFSK-1	brain:	n/a
19	chr11:17294197-17294247	IMR90	lung:	fetal
20	chr11:17298048-17298098	BE2_C	brain:	n/a
21	chr11:17253798-17253848	K562	blood:	n/a
22	chr11:17229012-17229062	GM12892	blood:	n/a
23	chr11:17300909-17300959	MCF10A-Er-Src	breast:	n/a
24	chr11:17298048-17298098	AG09319	gingival:	n/a
25	chr11:17191617-17191667	SK-N-SH_RA	brain:	n/a
26	chr11:17297732-17297782	NH-A	brain:	n/a
27	chr11:17229115-17229165	AoSMC	blood vessel:	n/a
28	chr11:17298273-17298323	HCPEpiC	choroid plexus:	n/a
29	chr11:17298064-17298114	GM12891	blood:	n/a
30	chr11:17229523-17229573	GM12892	blood:	n/a
31	chr11:17229731-17229781	NB4	blood:	n/a
32	chr11:17251956-17252006	SKMC	muscle:	n/a
33	chr11:17230092-17230142	H1-hESC	embryonic stem cell:	embryo
34	chr11:17249882-17249932	AG10803	skin:	n/a
35	chr11:17298266-17298316	HNPCEpiC	eye:	n/a
36	chr11:17298048-17298098	H1-hESC	embryonic stem cell:	embryo
37	chr11:17249967-17250017	H1-hESC	embryonic stem cell:	embryo
38	chr11:17298260-17298310	ECC-1	luminal epithelium:	n/a
39	chr11:17298347-17298397	HL-60	blood:	n/a
40	chr11:17249958-17250008	IMR90	lung:	fetal
41	chr11:17191617-17191667	NH-A	brain:	n/a
42	chr11:17207724-17207774	ECC-1	luminal epithelium:	n/a
43	chr11:17229115-17229165	PANC-1	pancreas:	n/a
44	chr11:17192372-17192422	K562	blood:	n/a
45	chr11:17229674-17229724	HRE	kidney:	n/a
46	chr11:17192372-17192422	SK-N-SH_RA	brain:	n/a
47	chr11:17249882-17249932	HCPEpiC	choroid plexus:	n/a
48	chr11:17230092-17230142	AG04450	lung:	fetal
49	chr11:17298266-17298316	HCPEpiC	choroid plexus:	n/a
50	chr11:17230092-17230142	HEEpiC	esophagus:	n/a

(count:144 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:17097586..17100321-chr11:17230835..17232404,2	K562	blood:
2	chr11:17297839..17299498-chr11:17314289..17315941,2	K562	blood:
3	chr11:17237750..17239535-chr11:17241512..17245226,3	MCF-7	breast:
4	chr11:17214868..17217658-chr11:17229098..17231108,2	MCF-7	breast:
5	chr11:17284490..17286833-chr11:17298188..17300234,2	K562	blood:
6	chr11:17260848..17261373-chr11:17294457..17295035,2	MCF-7	breast:
7	chr11:17097070..17101102-chr11:17296326..17299484,3	K562	blood:
8	chr11:17260848..17261450-chr11:17294076..17295035,3	MCF-7	breast:
9	chr11:17200195..17203044-chr11:17207705..17210741,3	K562	blood:
10	chr11:17237750..17239535-chr11:17241512..17245226,3	MCF-7	breast:
11	chr11:17227592..17232225-chr11:17372606..17377021,9	K562	blood:
12	chr11:17287872..17290107-chr11:17373411..17375142,2	K562	blood:
13	chr11:17193774..17196751-chr11:17204153..17207102,2	K562	blood:
14	chr11:17229045..17230754-chr11:17298034..17300385,2	MCF-7	breast:
15	chr11:17232194..17233796-chr11:17514149..17515893,2	MCF-7	breast:
16	chr11:17229956..17230914-chr2:11484768..11485358,2	Hela-S3	cervix:
17	chr11:17217666..17220812-chr11:17226929..17230937,4	MCF-7	breast:
18	chr11:17276902..17279261-chr11:17279604..17281506,2	K562	blood:
19	chr11:17201544..17204843-chr11:17207859..17210741,3	K562	blood:
20	chr11:17219025..17222560-chr11:17227070..17230586,4	K562	blood:
21	chr11:17237703..17242484-chr11:17242946..17247275,6	K562	blood:
22	chr11:17230708..17231299-chr13:110132822..110133342,2	Hela-S3	cervix:
23	chr11:17207589..17210389-chr11:17212889..17214960,2	MCF-7	breast:
24	chr1:36689400..36690646-chr11:17228897..17229639,3	Hela-S3	cervix:
25	chr11:17308283..17309860-chr11:17310824..17312984,2	K562	blood:
26	chr11:17298938..17303193-chr11:17304940..17310347,8	K562	blood:
27	chr11:17214868..17217658-chr11:17229098..17231108,2	MCF-7	breast:
28	chr11:17206803..17209141-chr11:17217436..17220407,2	MCF-7	breast:
29	chr11:17290835..17293391-chr11:17295443..17297735,3	K562	blood:
30	chr1:236030459..236030960-chr11:17297574..17298074,2	Hela-S3	cervix:
31	chr11:17181778..17184549-chr11:17240618..17243052,2	K562	blood:
32	chr11:17096429..17100576-chr11:17227768..17230724,6	K562	blood:
33	chr11:17296529..17299421-chr11:17301500..17303584,3	K562	blood:
34	chr11:17182736..17185668-chr11:17187012..17188861,2	K562	blood:
35	chr11:17238056..17240462-chr11:17259257..17260894,2	K562	blood:
36	chr11:17270890..17273003-chr11:17372999..17375299,2	K562	blood:
37	chr11:17196415..17198675-chr11:17200267..17202983,2	K562	blood:
38	chr11:17183106..17184886-chr11:17186963..17189434,2	MCF-7	breast:
39	chr11:17294885..17299963-chr11:17371989..17377835,11	K562	blood:
40	chr11:17278678..17282640-chr11:17283313..17286306,4	K562	blood:
41	chr11:17191444..17193638-chr17:59471300..59473152,2	MCF-7	breast:
42	chr11:17099103..17100814-chr11:17219601..17221116,2	MCF-7	breast:
43	chr11:17097742..17101154-chr11:17227974..17231312,6	MCF-7	breast:
44	chr11:17230080..17232225-chr11:17374978..17377752,3	K562	blood:
45	chr11:17297226..17298077-chr5:43007702..43008379,2	NB4	blood:
46	chr11:17229455..17230019-chr20:30194667..30195263,2	Hela-S3	cervix:
47	chr11:17172410..17175625-chr11:17176189..17178392,3	MCF-7	breast:
48	chr11:17296907..17298912-chr11:17352213..17353767,2	K562	blood:
49	chr11:17231042..17233596-chr11:17296907..17299193,2	MCF-7	breast:
50	chr1:36771726..36772530-chr11:17229104..17229999,2	Hela-S3	cervix:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP1-239B22.1.1-2	chr11:17298278-17298375	NONHSAT018222
2	lnc-RP1-239B22.1.1-2	chr11:17317652-17317713	NONHSAT018223
3	lnc-RP1-239B22.1.1-2	chr11:17299909-17300084	NONHSAT018222
4	lnc-KCNJ11-5	chr11:17315881-17316560	l_439_chr11:17315763-17328093_testes
5	lnc-RP1-239B22.1.1-2	chr11:17298287-17298395	NONHSAT018223
6	lnc-NUCB2-5	chr11:17215468-17215855	NONHSAT018217
7	lnc-RP1-239B22.1.1-2	chr11:17304337-17304490	NONHSAT018223
8	lnc-KCNJ11-5	chr11:17315764-17315875	l_439_chr11:17315763-17328093_testes
9	lnc-NUCB2-5	chr11:17215036-17215101	NONHSAT018217
10	lnc-RP1-239B22.1.1-2	chr11:17304336-17304417	NONHSAT018222
11	lnc-RP1-239B22.1.1-2	chr11:17316872-17317014	NONHSAT018223
12	lnc-NUCB2-4	chr11:17229653-17230826	NONHSAT018219
13	lnc-RP1-239B22.1.1-3	chr11:17230981-17236657	NONHSAT018220

No data

Variant related genes	Relation type
ENSG00000213779	TF binding region
NUCB2	TF binding region
ENSG00000197149	TF binding region
PIK3C2A	TF binding region
ENSG00000213779	CpG island
NUCB2	CpG island
ENSG00000197149	CpG island
PIK3C2A	CpG island
ENSG00000272034	chromatin interactions
ENSG00000197747	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000256206	chromatin interactions
ENSG00000187486	chromatin interactions
ENSG00000188211	chromatin interactions
ENSG00000110700	chromatin interactions
ENSG00000011405	chromatin interactions
ENSG00000158467	chromatin interactions
ENSG00000180596	chromatin interactions
ENSG00000054118	chromatin interactions
ENSG00000221322	chromatin interactions
ENSG00000110958	chromatin interactions
ENSG00000129084	chromatin interactions
ENSG00000188229	chromatin interactions
ENSG00000070081	chromatin interactions
ENSG00000214193	chromatin interactions
ENSG00000264395	chromatin interactions
ENSG00000180573	chromatin interactions
ENSG00000129158	chromatin interactions
ENSG00000165487	chromatin interactions
ENSG00000201403	chromatin interactions
ENSG00000213779	chromatin interactions

Extended variants
information (count: 5415 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:5415 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577176355	chr11:17170700-17170701	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs374735634	chr11:17170724-17170725	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs564305412	chr11:17170726-17170727	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141265091	chr11:17170785-17170786	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs550008650	chr11:17170837-17170838	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568138890	chr11:17170839-17170840	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs568417419	chr11:17170851-17170852	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190880340	chr11:17170857-17170858	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs547324704	chr11:17170859-17170860	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146925563	chr11:17170876-17170877	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs147974022	chr11:17170878-17170879	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs557454711	chr11:17170910-17170911	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558070380	chr11:17170918-17170919	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575833863	chr11:17170932-17170933	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370463467	chr11:17170958-17170959	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537236482	chr11:17170999-17171000	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374685205	chr11:17171009-17171010	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs140723687	chr11:17171010-17171011	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs34137650	chr11:17171028-17171029	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs372185739	chr11:17171113-17171114	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs542834576	chr11:17171116-17171117	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs183745149	chr11:17171119-17171120	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541959032	chr11:17171140-17171141	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs560509492	chr11:17171172-17171173	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs369773065	chr11:17171218-17171219	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561565829	chr11:17171239-17171240	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs562411526	chr11:17171243-17171244	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs150156157	chr11:17171251-17171252	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545826355	chr11:17171263-17171264	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs12291221	chr11:17171278-17171279	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs138646036	chr11:17171337-17171338	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs141739345	chr11:17171338-17171339	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs35822532	chr11:17171465-17171466	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188277078	chr11:17171513-17171514	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540969969	chr11:17171532-17171533	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs61879715	chr11:17171537-17171538	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs193060261	chr11:17171561-17171562	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs565804717	chr11:17171589-17171590	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs532939513	chr11:17171703-17171704	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs551440794	chr11:17171795-17171796	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs12291496	chr11:17171819-17171820	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs550984102	chr11:17171838-17171839	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs564508825	chr11:17171863-17171864	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs555489397	chr11:17171887-17171888	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs12365283	chr11:17171902-17171903	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs567370289	chr11:17171906-17171907	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs535908466	chr11:17171953-17171954	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs74418868	chr11:17171956-17171957	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs146254453	chr11:17171990-17171991	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs572234768	chr11:17171997-17171998	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
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
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:3613 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17105400-17172800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:17108200-17177400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:17108600-17172800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr11:17111600-17182000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr11:17120400-17181600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr11:17120800-17171800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr11:17120800-17172200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr11:17121000-17178000	Weak transcription	Psoas Muscle	Psoas
9	chr11:17125400-17172200	Weak transcription	Fetal Brain Male	brain
10	chr11:17125800-17181400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr11:17126800-17186400	Weak transcription	Colonic Mucosa	Colon
12	chr11:17130200-17174600	Weak transcription	Spleen	Spleen
13	chr11:17130200-17203800	Weak transcription	Aorta	Aorta
14	chr11:17139000-17171200	Weak transcription	Fetal Brain Female	brain
15	chr11:17140000-17183400	Weak transcription	Small Intestine	intestine
16	chr11:17144200-17192800	Weak transcription	NHDF-Ad	bronchial
17	chr11:17150800-17172000	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr11:17150800-17186000	Weak transcription	NHLF	lung
19	chr11:17151000-17173200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr11:17156400-17186400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr11:17156400-17186600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr11:17156600-17172600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr11:17156600-17172800	Weak transcription	Brain Angular Gyrus	brain
24	chr11:17156600-17175400	Weak transcription	Esophagus	oesophagus
25	chr11:17156600-17180800	Weak transcription	Colon Smooth Muscle	Colon
26	chr11:17156600-17182400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr11:17156600-17183600	Weak transcription	Lung	lung
28	chr11:17156600-17219200	Weak transcription	HSMMtube	muscle
29	chr11:17156800-17172200	Weak transcription	Brain Hippocampus Middle	brain
30	chr11:17156800-17181000	Weak transcription	Brain Germinal Matrix	brain
31	chr11:17157000-17175400	Weak transcription	K562	blood
32	chr11:17158000-17215600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr11:17158600-17173200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr11:17159400-17176000	Strong transcription	Monocytes-CD14+_RO01746	blood
35	chr11:17159800-17173200	Strong transcription	HUES64 Cell Line	embryonic stem cell
36	chr11:17160600-17171000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr11:17161200-17171800	Strong transcription	Liver	Liver
38	chr11:17162200-17174000	Strong transcription	Primary T helper cells fromperipheralblood	blood
39	chr11:17163200-17174600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr11:17163800-17172200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr11:17164400-17181200	Weak transcription	Gastric	stomach
42	chr11:17164400-17186200	Weak transcription	A549	lung
43	chr11:17164600-17172000	Weak transcription	Brain Substantia Nigra	brain
44	chr11:17165000-17176000	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr11:17165200-17172000	Weak transcription	Brain Cingulate Gyrus	brain
46	chr11:17165200-17180600	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr11:17165200-17215200	Weak transcription	Rectal Smooth Muscle	rectum
48	chr11:17165400-17170800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr11:17166200-17190200	Weak transcription	NH-A	brain
50	chr11:17166400-17183600	Weak transcription	Fetal Intestine Small	intestine

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