Variant report

Variant	esv1810781
Chromosome Location	chr11:76311021-76464814
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3454)
CpG islands
(count:3603)
Chromatin interactive
region (count:162)
LncRNA
region (count:36)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:3454 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:76411687-76411745	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:76458629-76458856	K562	blood:	n/a	n/a
3	ARID3A	chr11:76446949-76447230	K562	blood:	n/a	n/a
4	ARID3A	chr11:76456593-76457227	K562	blood:	n/a	n/a
5	ARID3A	chr11:76413512-76414223	K562	blood:	n/a	n/a
6	ARID3A	chr11:76410896-76411918	K562	blood:	n/a	n/a
7	ARID3A	chr11:76391998-76392112	HepG2	liver:	n/a	n/a
8	ATF1	chr11:76413512-76414181	K562	blood:	n/a	n/a
9	ATF1	chr11:76446898-76447251	K562	blood:	n/a	n/a
10	ATF1	chr11:76425666-76425868	K562	blood:	n/a	n/a
11	ATF1	chr11:76411479-76412165	K562	blood:	n/a	n/a
12	ATF1	chr11:76456584-76457197	K562	blood:	n/a	n/a
13	ATF1	chr11:76355637-76355872	K562	blood:	n/a	n/a
14	ATF2	chr11:76415232-76415719	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr11:76385546-76386067	GM12878	blood:	n/a	n/a
16	ATF2	chr11:76348494-76348928	GM12878	blood:	n/a	n/a
17	ATF2	chr11:76383568-76384253	GM12878	blood:	n/a	n/a
18	ATF2	chr11:76337886-76338400	GM12878	blood:	n/a	n/a
19	ATF2	chr11:76383508-76384302	GM12878	blood:	n/a	n/a
20	ATF2	chr11:76337780-76338399	GM12878	blood:	n/a	n/a
21	ATF3	chr11:76446942-76447222	K562	blood:	n/a	n/a
22	ATF3	chr11:76413425-76414197	K562	blood:	n/a	n/a
23	ATF3	chr11:76411568-76411964	K562	blood:	n/a	n/a
24	ATF3	chr11:76411451-76411909	K562	blood:	n/a	n/a
25	BACH1	chr11:76415213-76415489	K562	blood:	n/a	n/a
26	BACH1	chr11:76451851-76452356	K562	blood:	n/a	n/a
27	BACH1	chr11:76396644-76396649	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr11:76411476-76411994	K562	blood:	n/a	n/a
29	BACH1	chr11:76414987-76415714	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr11:76388073-76388209	K562	blood:	n/a	n/a
31	BACH1	chr11:76447086-76447173	K562	blood:	n/a	n/a
32	BACH1	chr11:76413519-76413980	K562	blood:	n/a	n/a
33	BACH1	chr11:76432882-76433121	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr11:76410019-76410236	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr11:76412721-76412818	K562	blood:	n/a	n/a
36	BACH1	chr11:76381231-76382296	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr11:76391763-76392056	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr11:76409302-76409696	H1-hESC	embryonic stem cell:	n/a	n/a
39	BATF	chr11:76385620-76385950	GM12878	blood:	n/a	n/a
40	BATF	chr11:76330901-76331291	GM12878	blood:	n/a	n/a
41	BATF	chr11:76383752-76384252	GM12878	blood:	n/a	n/a
42	BATF	chr11:76337962-76338326	GM12878	blood:	n/a	n/a
43	BATF	chr11:76337983-76338268	GM12878	blood:	n/a	n/a
44	BCL11A	chr11:76383689-76384113	GM12878	blood:	n/a	chr11:76383801-76383810
45	BCL11A	chr11:76330894-76331272	GM12878	blood:	n/a	n/a
46	BCL11A	chr11:76337930-76338357	GM12878	blood:	n/a	n/a
47	BCL11A	chr11:76385591-76386015	GM12878	blood:	n/a	n/a
48	BCL11A	chr11:76330948-76331211	GM12878	blood:	n/a	n/a
49	BCL11A	chr11:76337943-76338241	GM12878	blood:	n/a	n/a
50	BCL11A	chr11:76383625-76384124	GM12878	blood:	n/a	chr11:76383801-76383810

(count:3603 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:76320970-76321020	CMK	blood:	n/a
2	chr11:76464026-76464076	ovcar-3	ovarian:	n/a
3	chr11:76432800-76432850	AoSMC	blood vessel:	n/a
4	chr11:76401495-76401545	HL-60	blood:	n/a
5	chr11:76320970-76321020	CMK	blood:	n/a
6	chr11:76464026-76464076	ovcar-3	ovarian:	n/a
7	chr11:76432800-76432850	AoSMC	blood vessel:	n/a
8	chr11:76401495-76401545	HL-60	blood:	n/a
9	chr11:76455541-76455591	AoSMC	blood vessel:	n/a
10	chr11:76382128-76382178	ECC-1	luminal epithelium:	n/a
11	chr11:76320970-76321020	HCM	heart:	n/a
12	chr11:76327232-76327282	PANC-1	pancreas:	n/a
13	chr11:76410147-76410197	MCF10A-Er-Src	breast:	n/a
14	chr11:76381971-76382021	PANC-1	pancreas:	n/a
15	chr11:76376064-76376114	Jurkat	blood:	n/a
16	chr11:76327232-76327282	BJ	skin:	n/a
17	chr11:76367177-76367227	AG09309	skin:	n/a
18	chr11:76372128-76372178	NH-A	brain:	n/a
19	chr11:76377572-76377622	GM12892	blood:	n/a
20	chr11:76372128-76372178	AG04450	lung:	fetal
21	chr11:76432800-76432850	AG04450	lung:	fetal
22	chr11:76391253-76391303	AG04449	skin:	fetal
23	chr11:76414043-76414093	HUVEC	blood vessel:	n/a
24	chr11:76372128-76372178	A549	lung:	n/a
25	chr11:76348764-76348814	HEEpiC	esophagus:	n/a
26	chr11:76410147-76410197	HCM	heart:	n/a
27	chr11:76380921-76380971	Caco-2	colon:	n/a
28	chr11:76401495-76401545	NHBE	bronchial:	n/a
29	chr11:76381687-76381737	SK-N-SH_RA	brain:	n/a
30	chr11:76340765-76340815	ProgFib	skin:	n/a
31	chr11:76334450-76334500	PrEC	prostate:	n/a
32	chr11:76414043-76414093	A549	lung:	n/a
33	chr11:76370510-76370560	AG09319	gingival:	n/a
34	chr11:76340765-76340815	MCF10A-Er-Src	breast:	n/a
35	chr11:76430515-76430565	PrEC	prostate:	n/a
36	chr11:76381800-76381850	HPAEpiC	pulmonary alveolar:	n/a
37	chr11:76432847-76432897	BE2_C	brain:	n/a
38	chr11:76432983-76433033	AG09319	gingival:	n/a
39	chr11:76381148-76381198	HepG2	liver:	n/a
40	chr11:76411795-76411845	HPAEpiC	pulmonary alveolar:	n/a
41	chr11:76381165-76381215	Hela-S3	cervix:	n/a
42	chr11:76430375-76430425	PANC-1	pancreas:	n/a
43	chr11:76348764-76348814	GM19239	blood:	n/a
44	chr11:76319232-76319282	AG09309	skin:	n/a
45	chr11:76381791-76381841	A549	lung:	n/a
46	chr11:76446769-76446819	SK-N-SH	brain:	n/a
47	chr11:76381044-76381094	HCF	heart:	n/a
48	chr11:76432938-76432988	AG10803	skin:	n/a
49	chr11:76319232-76319282	CMK	blood:	n/a
50	chr11:76319232-76319282	BJ	skin:	n/a

(count:162 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr11:76432526..76433808-chr11:76756582..76757744,4	MCF-7	breast:
2	chr11:76309441..76311518-chr11:76311642..76314549,3	K562	blood:
3	chr11:76338138..76339963-chr11:76341531..76343151,2	K562	blood:
4	chr11:76444616..76445153-chr11:76518177..76519095,2	MCF-7	breast:
5	chr11:76402340..76404268-chr11:76405216..76407776,2	K562	blood:
6	chr11:76321340..76322129-chr11:76391843..76392519,2	MCF-7	breast:
7	chr11:76410635..76412831-chr11:76434613..76437612,2	K562	blood:
8	chr11:76417791..76419784-chr11:76428220..76430415,2	K562	blood:
9	chr11:76410199..76412182-chr11:76493840..76496513,2	K562	blood:
10	chr11:76309431..76311546-chr11:76315205..76316981,3	K562	blood:
11	chr11:76345088..76347686-chr11:76350787..76353535,2	K562	blood:
12	chr11:76457514..76460124-chr11:76468465..76470695,2	MCF-7	breast:
13	chr11:76451295..76455303-chr11:76456358..76459104,3	K562	blood:
14	chr11:76445248..76448071-chr11:76628717..76631883,4	MCF-7	breast:
15	chr11:76409188..76411296-chr11:76414786..76418251,3	MCF-7	breast:
16	chr11:76430934..76434920-chr11:76435609..76442633,7	MCF-7	breast:
17	chr11:76390604..76393512-chr11:76398509..76400952,3	MCF-7	breast:
18	chr11:76460876..76462909-chr11:76463917..76467153,3	MCF-7	breast:
19	chr11:76377677..76380472-chr11:76382073..76384375,3	K562	blood:
20	chr11:76364167..76367346-chr11:76381295..76383595,3	K562	blood:
21	chr11:76400510..76402600-chr11:76412670..76414402,2	MCF-7	breast:
22	chr11:76431666..76434446-chr11:76757030..76758684,2	K562	blood:
23	chr11:76309253..76310227-chr11:76391621..76392159,2	K562	blood:
24	chr11:76310504..76312351-chr11:76321930..76323768,2	K562	blood:
25	chr11:76445665..76448359-chr11:76459229..76461438,2	K562	blood:
26	chr11:76444662..76445640-chr11:76629853..76630608,2	MCF-7	breast:
27	chr11:76202482..76203428-chr11:76391378..76392425,4	MCF-7	breast:
28	chr11:76396498..76398290-chr11:76402831..76405192,3	K562	blood:
29	chr11:76404025..76406390-chr11:76409213..76412449,4	K562	blood:
30	chr11:76446515..76448277-chr11:76483918..76485534,2	MCF-7	breast:
31	chr11:76378581..76380312-chr11:76384470..76387173,2	K562	blood:
32	chr11:76409927..76411663-chr11:76416991..76419332,2	K562	blood:
33	chr11:76433483..76435648-chr11:76441734..76444276,2	K562	blood:
34	chr11:76444817..76447367-chr11:76477489..76481018,3	MCF-7	breast:
35	chr11:76445987..76448531-chr11:76494334..76496063,4	MCF-7	breast:
36	chr11:76433483..76435648-chr11:76441734..76444276,2	K562	blood:
37	chr11:76313070..76315285-chr11:76346641..76348994,2	MCF-7	breast:
38	chr11:76309744..76311546-chr11:76315205..76316740,2	K562	blood:
39	chr11:76309452..76310726-chr11:76391627..76392625,9	MCF-7	breast:
40	chr11:76289419..76290667-chr11:76391568..76392518,9	MCF-7	breast:
41	chr11:76331643..76333160-chr11:76333362..76334961,2	K562	blood:
42	chr11:76337563..76340451-chr11:76340690..76342431,2	MCF-7	breast:
43	chr11:76350867..76353038-chr11:76535438..76537747,2	MCF-7	breast:
44	chr11:75918371..75919261-chr11:76391667..76392614,4	MCF-7	breast:
45	chr11:76451295..76455303-chr11:76456358..76459104,3	K562	blood:
46	chr11:76444797..76445605-chr11:76756797..76757751,2	K562	blood:
47	chr11:76396498..76398290-chr11:76402831..76405192,3	K562	blood:
48	chr11:76426123..76429227-chr11:76433055..76436273,3	K562	blood:
49	chr11:76450173..76453012-chr11:76491965..76494864,2	K562	blood:
50	chr11:76313070..76315285-chr11:76346641..76348994,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C11orf30-1	chr11:76373673-76374910	ENSG00000236304.1
2	lnc-TSKU-2	chr11:76463774-76463945	XLOC_009221
3	lnc-LRRC32-4	chr11:76414379-76414571	NR_024042
4	lnc-LRRC32-4	chr11:76406407-76406593	NR_024042
5	lnc-TSKU-3	chr11:76414016-76414239	ENSG00000254975
6	lnc-LRRC32-4	chr11:76407785-76407959	NR_024042
7	lnc-TSKU-3	chr11:76386123-76386230	ENSG00000254975
8	lnc-LRRC32-4	chr11:76415205-76415368	NR_024042
9	lnc-LRRC32-4	chr11:76427774-76427942	NR_024042
10	lnc-PRKRIR-4	chr11:76376915-76377015	NONHSAT023179
11	lnc-LRRC32-4	chr11:76405582-76405703	NR_024042
12	lnc-LRRC32-4	chr11:76427453-76427505	NR_024042
13	lnc-LRRC32-1	chr11:76367493-76367756	ENSG00000254810
14	lnc-LRRC32-4	chr11:76427590-76427686	NR_024042
15	lnc-LRRC32-4	chr11:76430542-76430909	NR_024042
16	lnc-LRRC32-4	chr11:76391210-76391413	NR_024042
17	lnc-LRRC32-4	chr11:76419294-76419486	NR_024042
18	lnc-LRRC32-4	chr11:76405102-76405179	NR_024042
19	lnc-LRRC32-2	chr11:76339140-76339525	ENSG00000255363
20	lnc-LRRC32-4	chr11:76402648-76402732	NR_024042
21	lnc-LRRC32-4	chr11:76428978-76429070	NR_024042
22	lnc-LRRC32-4	chr11:76423440-76424230	ENSG00000254761
23	lnc-LRRC32-4	chr11:76430612-76430652	ENSG00000254761
24	lnc-TSKU-3	chr11:76398802-76398921	ENSG00000254975
25	lnc-LRRC32-2	chr11:76341235-76341407	ENSG00000255363
26	lnc-PRKRIR-4	chr11:76368614-76369078	NONHSAT023179
27	lnc-LRRC32-4	chr11:76423311-76423459	NR_024042
28	lnc-LRRC32-4	chr11:76432751-76432833	NR_024042
29	lnc-LRRC32-4	chr11:76400079-76400271	NR_024042
30	lnc-LRRC32-4	chr11:76418549-76418605	NR_024042
31	lnc-LRRC32-1	chr11:76365213-76365599	ENSG00000254810
32	lnc-C11orf30-1	chr11:76370652-76370738	ENSG00000236304.1
33	lnc-LRRC32-4	chr11:76393818-76393844	NR_024042
34	lnc-C11orf30-1	chr11:76368100-76368200	ENSG00000236304.1
35	lnc-LRRC32-4	chr11:76423760-76423788	NR_024042
36	lnc-LRRC32-4	chr11:76418650-76418729	NR_024042

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	LRRC32	hsa-miR-335-5p	chr11:76369370-76369393

Variant related genes	Relation type
ENSG00000255479	TF binding region
ENSG00000255363	TF binding region
ENSG00000254975	TF binding region
ENSG00000236304	TF binding region
ENSG00000254810	TF binding region
LRRC32	TF binding region
GUCY2EP	TF binding region
ENSG00000254761	TF binding region
ENSG00000255479	CpG island
ENSG00000255363	CpG island
ENSG00000254975	CpG island
ENSG00000236304	CpG island
ENSG00000254810	CpG island
LRRC32	CpG island
GUCY2EP	CpG island
ENSG00000254761	CpG island
ENSG00000236304	chromatin interactions
ENSG00000255479	chromatin interactions
ENSG00000161016	chromatin interactions
ENSG00000137507	chromatin interactions
ENSG00000254810	chromatin interactions
ENSG00000078124	chromatin interactions
ENSG00000254755	chromatin interactions
ENSG00000254975	chromatin interactions
ENSG00000254632	chromatin interactions
ENSG00000182704	chromatin interactions
ENSG00000255100	chromatin interactions
ENSG00000204529	chromatin interactions
ENSG00000255363	chromatin interactions

Extended variants
information (count: 6730 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:6730 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552237399	chr11:76311033-76311034	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs187102830	chr11:76311045-76311046	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs531405810	chr11:76311084-76311085	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs7110364	chr11:76311139-76311140	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs548512900	chr11:76311172-76311173	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs370509904	chr11:76311249-76311250	Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs534498576	chr11:76311300-76311301	Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs78090132	chr11:76311301-76311302	Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs576895601	chr11:76311338-76311339	Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs55778917	chr11:76311356-76311357	Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs553321644	chr11:76311400-76311401	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs556199727	chr11:76311404-76311405	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs576073957	chr11:76311443-76311444	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs371889463	chr11:76311456-76311457	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs544070891	chr11:76311469-76311470	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs115717011	chr11:76311492-76311493	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs114129291	chr11:76311555-76311556	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs565351734	chr11:76311598-76311599	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs191136149	chr11:76311605-76311606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs7124842	chr11:76311620-76311621	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs532349764	chr11:76311683-76311684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555012554	chr11:76311765-76311766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs201156905	chr11:76311802-76311803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs72002067	chr11:76311808-76311809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550624980	chr11:76311814-76311815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371974372	chr11:76311840-76311841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562965192	chr11:76311853-76311854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531720147	chr11:76311855-76311856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs199534994	chr11:76311856-76311857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs57630987	chr11:76311857-76311858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11236799	chr11:76311865-76311866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369024676	chr11:76311866-76311867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7111295	chr11:76311867-76311868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs202173897	chr11:76311868-76311869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35290255	chr11:76311869-76311870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs149082847	chr11:76311871-76311872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72021689	chr11:76311891-76311892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565662887	chr11:76311892-76311893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12223824	chr11:76311894-76311895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548714822	chr11:76311899-76311900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs181584133	chr11:76311927-76311928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186350020	chr11:76311944-76311945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371894433	chr11:76311949-76311950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs9645696	chr11:76311991-76311992	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs374744709	chr11:76312029-76312030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189554865	chr11:76312040-76312041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs559110095	chr11:76312081-76312082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs199635137	chr11:76312176-76312177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs11236800	chr11:76312270-76312271	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs12099277	chr11:76312307-76312308	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:101)

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
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
Melanoma	18172304	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
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21482786	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	16608533	CNVD
Usher syndrome	18421352	CNVD
Ovarian cancer	21240255	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	22355333	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3288 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76303200-76313600	Weak transcription	Gastric	stomach
2	chr11:76303200-76315600	Weak transcription	Brain Angular Gyrus	brain
3	chr11:76303600-76315800	Weak transcription	Esophagus	oesophagus
4	chr11:76304200-76312600	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr11:76304200-76313200	Weak transcription	Stomach Mucosa	stomach
6	chr11:76304400-76313400	Weak transcription	Colonic Mucosa	Colon
7	chr11:76304400-76315600	Weak transcription	Pancreas	Pancrea
8	chr11:76305000-76312800	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr11:76308800-76311400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr11:76309200-76311200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr11:76309200-76311400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr11:76309600-76311200	Enhancers	NH-A	brain
13	chr11:76309600-76313000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr11:76309600-76313200	Weak transcription	Left Ventricle	heart
15	chr11:76309800-76313400	Weak transcription	Fetal Thymus	thymus
16	chr11:76309800-76313400	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr11:76310200-76311200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr11:76310200-76312800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr11:76310400-76311200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr11:76310400-76312800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr11:76310400-76313400	Weak transcription	Fetal Lung	lung
22	chr11:76310400-76313400	Weak transcription	Right Ventricle	heart
23	chr11:76310400-76315600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr11:76310600-76311400	Enhancers	Lung	lung
25	chr11:76310600-76312800	Weak transcription	Fetal Heart	heart
26	chr11:76310600-76313200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr11:76310600-76313200	Weak transcription	Duodenum Mucosa	Duodenum
28	chr11:76310600-76313400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr11:76310600-76313400	Weak transcription	Spleen	Spleen
30	chr11:76310600-76313600	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr11:76310600-76320200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr11:76310800-76311400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr11:76310800-76312600	Weak transcription	Fetal Stomach	stomach
34	chr11:76310800-76312600	Weak transcription	NHLF	lung
35	chr11:76310800-76312800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr11:76310800-76312800	Weak transcription	Stomach Smooth Muscle	stomach
37	chr11:76310800-76313400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr11:76310800-76313400	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr11:76310800-76313800	Weak transcription	Osteobl	bone
40	chr11:76311000-76312400	Weak transcription	Placenta	Placenta
41	chr11:76311000-76312800	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr11:76311000-76313000	Weak transcription	NHDF-Ad	bronchial
43	chr11:76311000-76313400	Weak transcription	Fetal Muscle Trunk	muscle
44	chr11:76311000-76313600	Weak transcription	Small Intestine	intestine
45	chr11:76311200-76311400	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr11:76311200-76311400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr11:76311200-76314000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr11:76311200-76320800	Weak transcription	NH-A	brain
49	chr11:76311400-76311600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr11:76311400-76312400	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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