Variant report

Variant	nsv1044943
Chromosome Location	chr11:75872758-75922912
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1224)
CpG islands
(count:2509)
Chromatin interactive
region (count:86)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1224 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:75919860-75920108	HepG2	liver:	n/a	n/a
2	ATF2	chr11:75877385-75877776	GM12878	blood:	n/a	n/a
3	ATF2	chr11:75877442-75877843	GM12878	blood:	n/a	n/a
4	ATF3	chr11:75919853-75920215	A549	lung:	n/a	n/a
5	ATF3	chr11:75919783-75920220	A549	lung:	n/a	n/a
6	BACH1	chr11:75919833-75920847	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr11:75921380-75922316	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr11:75916750-75916926	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr11:75918583-75919316	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr11:75918709-75918900	K562	blood:	n/a	n/a
11	BATF	chr11:75880537-75880793	GM12878	blood:	n/a	n/a
12	BATF	chr11:75877503-75877745	GM12878	blood:	n/a	n/a
13	BATF	chr11:75880507-75880811	GM12878	blood:	n/a	n/a
14	BATF	chr11:75877452-75877791	GM12878	blood:	n/a	n/a
15	BCL11A	chr11:75877450-75877789	GM12878	blood:	n/a	chr11:75877743-75877752
16	BCL11A	chr11:75877511-75877755	GM12878	blood:	n/a	chr11:75877743-75877752
17	BCL11A	chr11:75880481-75880847	GM12878	blood:	n/a	chr11:75880797-75880806
18	BCL3	chr11:75918338-75918916	A549	lung:	n/a	chr11:75918813-75918822
19	BCL3	chr11:75919791-75920256	A549	lung:	n/a	chr11:75919827-75919836
20	BHLHE40	chr11:75895960-75896047	K562	blood:	n/a	n/a
21	BHLHE40	chr11:75879567-75879848	K562	blood:	n/a	n/a
22	BHLHE40	chr11:75918605-75918909	K562	blood:	n/a	n/a
23	BHLHE40	chr11:75877454-75877762	GM12878	blood:	n/a	n/a
24	BHLHE40	chr11:75917520-75917589	GM12878	blood:	n/a	chr11:75917535-75917551
25	BHLHE40	chr11:75874344-75874627	K562	blood:	n/a	chr11:75874506-75874515 chr11:75874499-75874520 chr11:75874505-75874514 chr11:75874505-75874514 chr11:75874504-75874513
26	BHLHE40	chr11:75874450-75874566	GM12878	blood:	n/a	chr11:75874506-75874515 chr11:75874499-75874520 chr11:75874505-75874514 chr11:75874505-75874514 chr11:75874504-75874513
27	BHLHE40	chr11:75921554-75922195	HepG2	liver:	n/a	chr11:75921944-75921960 chr11:75921941-75921957
28	BHLHE40	chr11:75918623-75918961	GM12878	blood:	n/a	n/a
29	BHLHE40	chr11:75874343-75874668	HepG2	liver:	n/a	chr11:75874506-75874515 chr11:75874499-75874520 chr11:75874505-75874514 chr11:75874505-75874514 chr11:75874504-75874513
30	BHLHE40	chr11:75919847-75920073	GM12878	blood:	n/a	n/a
31	BHLHE40	chr11:75880588-75880997	GM12878	blood:	n/a	n/a
32	BHLHE40	chr11:75917372-75917610	K562	blood:	n/a	chr11:75917535-75917551
33	BHLHE40	chr11:75918652-75918875	HepG2	liver:	n/a	n/a
34	BRCA1	chr11:75918536-75918947	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr11:75919889-75920503	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr11:75917362-75917369	Hela-S3	cervix:	n/a	n/a
37	CBX3	chr11:75918218-75918990	K562	blood:	n/a	n/a
38	CBX3	chr11:75917274-75917681	K562	blood:	n/a	n/a
39	CBX3	chr11:75873978-75874336	K562	blood:	n/a	n/a
40	CCNT2	chr11:75918618-75918977	K562	blood:	n/a	chr11:75918965-75918974
41	CCNT2	chr11:75895841-75896045	K562	blood:	n/a	n/a
42	CCNT2	chr11:75917343-75917789	K562	blood:	n/a	n/a
43	CEBPB	chr11:75919827-75920136	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr11:75895861-75896066	K562	blood:	n/a	n/a
45	CEBPB	chr11:75901486-75901900	IMR90	lung:	n/a	n/a
46	CEBPB	chr11:75918338-75918535	HepG2	liver:	n/a	n/a
47	CEBPB	chr11:75917020-75917495	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr11:75918220-75919075	A549	lung:	n/a	n/a
49	CEBPB	chr11:75918279-75918452	K562	blood:	n/a	n/a
50	CEBPB	chr11:75917830-75918975	Hela-S3	cervix:	n/a	n/a

(count:2509 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:75875926-75875976	HRCEpiC	kidney:	n/a
2	chr11:75921808-75921858	Hepatocyte	liver:	n/a
3	chr11:75905718-75905768	BE2_C	brain:	n/a
4	chr11:75902270-75902320	HCF	heart:	n/a
5	chr11:75873027-75873077	HL-60	blood:	n/a
6	chr11:75909015-75909065	ovcar-3	ovarian:	n/a
7	chr11:75921808-75921858	HPAEpiC	pulmonary alveolar:	n/a
8	chr11:75918630-75918680	HepG2	liver:	n/a
9	chr11:75875926-75875976	HRCEpiC	kidney:	n/a
10	chr11:75921808-75921858	Hepatocyte	liver:	n/a
11	chr11:75905718-75905768	BE2_C	brain:	n/a
12	chr11:75902270-75902320	HCF	heart:	n/a
13	chr11:75873027-75873077	HL-60	blood:	n/a
14	chr11:75909015-75909065	ovcar-3	ovarian:	n/a
15	chr11:75921808-75921858	HPAEpiC	pulmonary alveolar:	n/a
16	chr11:75918630-75918680	HepG2	liver:	n/a
17	chr11:75919130-75919180	NHDF-neo	bronchial:	n/a
18	chr11:75875926-75875976	HNPCEpiC	eye:	n/a
19	chr11:75907205-75907255	HUVEC	blood vessel:	n/a
20	chr11:75920278-75920328	H1-hESC	embryonic stem cell:	embryo
21	chr11:75905718-75905768	NHBE	bronchial:	n/a
22	chr11:75914370-75914420	HRPEpiC	eye:	n/a
23	chr11:75917404-75917454	Jurkat	blood:	n/a
24	chr11:75904184-75904234	AG04449	skin:	fetal
25	chr11:75919130-75919180	SK-N-MC	brain:	n/a
26	chr11:75898132-75898182	HNPCEpiC	eye:	n/a
27	chr11:75905718-75905768	A549	lung:	n/a
28	chr11:75873027-75873077	NT2-D1	testis:	n/a
29	chr11:75914370-75914420	Caco-2	colon:	n/a
30	chr11:75879348-75879398	SK-N-SH_RA	brain:	n/a
31	chr11:75917404-75917454	SKMC	muscle:	n/a
32	chr11:75904184-75904234	T-47D	breast:	n/a
33	chr11:75916460-75916510	AG04449	skin:	fetal
34	chr11:75875926-75875976	ECC-1	luminal epithelium:	n/a
35	chr11:75917404-75917454	GM12891	blood:	n/a
36	chr11:75917724-75917774	SAEC	small airway:	n/a
37	chr11:75921810-75921860	AoSMC	blood vessel:	n/a
38	chr11:75909015-75909065	HCT-116	colon:	n/a
39	chr11:75922172-75922222	A549	lung:	n/a
40	chr11:75898195-75898245	Hepatocyte	liver:	n/a
41	chr11:75878127-75878177	HEK293	kidney:	embryo
42	chr11:75905850-75905900	PANC-1	pancreas:	n/a
43	chr11:75919862-75919912	HRCEpiC	kidney:	n/a
44	chr11:75917982-75918032	K562	blood:	n/a
45	chr11:75920233-75920283	NT2-D1	testis:	n/a
46	chr11:75875926-75875976	PrEC	prostate:	n/a
47	chr11:75898203-75898253	AoSMC	blood vessel:	n/a
48	chr11:75905850-75905900	NB4	blood:	n/a
49	chr11:75897427-75897477	CMK	blood:	n/a
50	chr11:75896332-75896382	GM12892	blood:	n/a

(count:86 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:75919700..75922037-chr11:76092044..76093720,2	MCF-7	breast:
2	chr11:75918308..75919483-chr11:76029559..76030293,4	MCF-7	breast:
3	chr11:75891012..75893171-chr11:75895940..75897806,2	K562	blood:
4	chr11:75918736..75920705-chr11:76028307..76032444,3	MCF-7	breast:
5	chr11:75913612..75915944-chr11:75916007..75917749,2	K562	blood:
6	chr1:156698046..156698801-chr11:75908969..75909469,2	Hela-S3	cervix:
7	chr11:75917185..75919350-chr11:75920586..75922926,4	K562	blood:
8	chr11:75526830..75528448-chr11:75885826..75888721,2	K562	blood:
9	chr11:75867883..75870652-chr11:75871506..75874252,2	MCF-7	breast:
10	chr11:75871119..75872885-chr11:75874380..75876840,2	MCF-7	breast:
11	chr11:75918371..75919261-chr11:76391667..76392614,4	MCF-7	breast:
12	chr11:75895372..75898295-chr11:75906346..75908229,2	K562	blood:
13	chr11:75888382..75891358-chr11:75893738..75896231,2	MCF-7	breast:
14	chr11:75864698..75867155-chr11:75871013..75872936,2	MCF-7	breast:
15	chr11:75915411..75918045-chr11:75920337..75923182,4	MCF-7	breast:
16	chr11:75913811..75916068-chr11:75920291..75921987,2	K562	blood:
17	chr11:75881616..75884148-chr11:75897760..75900480,2	MCF-7	breast:
18	chr11:75878808..75880535-chr11:75885544..75887523,2	K562	blood:
19	chr11:75872410..75875308-chr11:75879381..75883436,3	K562	blood:
20	chr11:75908327..75910235-chr11:75911530..75913999,2	K562	blood:
21	chr11:75913174..75915616-chr11:76090569..76092152,2	MCF-7	breast:
22	chr11:75908327..75910235-chr11:75911530..75913999,2	K562	blood:
23	chr11:75871119..75872885-chr11:75874380..75876840,2	MCF-7	breast:
24	chr11:75874099..75876373-chr11:75881253..75883763,2	MCF-7	breast:
25	chr11:75915411..75918045-chr11:75920337..75923182,4	MCF-7	breast:
26	chr11:75887769..75890550-chr11:75903812..75906303,2	K562	blood:
27	chr11:75886596..75888940-chr11:75889618..75892110,2	MCF-7	breast:
28	chr11:75917185..75919350-chr11:75920586..75922926,4	K562	blood:
29	chr11:75907463..75909415-chr11:75917684..75920104,2	MCF-7	breast:
30	chr11:75862934..75863810-chr11:75918354..75919268,2	K562	blood:
31	chr11:75892849..75895480-chr11:75897932..75899434,2	K562	blood:
32	chr11:75895025..75897686-chr11:75910991..75913944,2	K562	blood:
33	chr11:75908679..75911274-chr11:75914998..75917762,2	K562	blood:
34	chr11:75896186..75898075-chr11:75909574..75912491,2	K562	blood:
35	chr11:75916539..75918756-chr11:75919573..75922083,2	MCF-7	breast:
36	chr11:75898285..75900069-chr11:75902238..75904019,2	K562	blood:
37	chr11:75907802..75910235-chr11:75912499..75914692,2	K562	blood:
38	chr11:75918865..75921360-chr11:76155223..76156994,2	MCF-7	breast:
39	chr11:75907463..75909415-chr11:75917684..75920104,2	MCF-7	breast:
40	chr11:75679088..75681419-chr11:75870768..75873220,2	K562	blood:
41	chr11:75878808..75880535-chr11:75885544..75887523,2	K562	blood:
42	chr11:75887769..75890550-chr11:75903812..75906303,2	K562	blood:
43	chr11:75865596..75868388-chr11:75876534..75879243,2	K562	blood:
44	chr11:75886513..75888497-chr11:75907057..75909283,2	MCF-7	breast:
45	chr11:75872410..75875308-chr11:75879381..75883436,3	K562	blood:
46	chr11:75892849..75895759-chr11:75897789..75899434,2	K562	blood:
47	chr11:75877596..75879712-chr11:75888366..75889930,2	K562	blood:
48	chr11:75919323..75921624-chr11:75923992..75926827,3	MCF-7	breast:
49	chr11:75888382..75891358-chr11:75893738..75896231,2	MCF-7	breast:
50	chr11:75918753..75920332-chr11:75923652..75925664,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKRIR-3	chr11:75917466-75917542	NONHSAT023149
2	lnc-UVRAG-2	chr11:75905685-75906115	ENSG00000254933.1
3	lnc-UVRAG-2	chr11:75901769-75901950	ENSG00000254933.1
4	lnc-PRKRIR-3	chr11:75921391-75921774	NONHSAT023149
5	lnc-WNT11-1	chr11:75922000-75922293	ENSG00000255362

No data

Variant related genes	Relation type
WNT11	TF binding region
ENSG00000254933	TF binding region
WNT11	CpG island
ENSG00000254933	CpG island
ENSG00000179240	chromatin interactions
ENSG00000137492	chromatin interactions
ENSG00000158636	chromatin interactions
ENSG00000143303	chromatin interactions
ENSG00000085741	chromatin interactions
ENSG00000143319	chromatin interactions
ENSG00000255135	chromatin interactions
ENSG00000254933	chromatin interactions

Extended variants
information (count: 2205 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:2205 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546103857	chr11:75872857-75872858	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
2	rs562979355	chr11:75872887-75872888	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
3	rs192942120	chr11:75872922-75872923	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
4	rs577966258	chr11:75872930-75872931	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
5	rs542197137	chr11:75872938-75872939	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
6	rs572166540	chr11:75872944-75872945	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
7	rs183849020	chr11:75872946-75872947	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
8	rs542672769	chr11:75873051-75873052	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs560829412	chr11:75873058-75873059	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs570038640	chr11:75873130-75873131	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs531162230	chr11:75873136-75873137	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs549361364	chr11:75873137-75873138	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs188668927	chr11:75873174-75873175	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs60924468	chr11:75873192-75873193	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs373576878	chr11:75873217-75873218	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
16	rs552119965	chr11:75873218-75873219	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
17	rs568923202	chr11:75873245-75873246	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
18	rs537587336	chr11:75873246-75873247	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
19	rs180771146	chr11:75873269-75873270	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
20	rs147451035	chr11:75873272-75873273	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
21	rs533788550	chr11:75873275-75873276	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
22	rs554479560	chr11:75873291-75873292	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
23	rs571191575	chr11:75873294-75873295	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
24	rs59983429	chr11:75873299-75873300	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs556520811	chr11:75873359-75873360	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
26	rs139907333	chr11:75873362-75873363	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
27	rs576479017	chr11:75873396-75873397	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
28	rs564573902	chr11:75873399-75873400	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
29	rs373168245	chr11:75873441-75873442	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
30	rs555456941	chr11:75873460-75873461	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
31	rs572079574	chr11:75873469-75873470	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
32	rs541054708	chr11:75873487-75873488	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
33	rs185266126	chr11:75873498-75873499	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
34	rs532342867	chr11:75873531-75873532	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
35	rs545973092	chr11:75873550-75873551	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
36	rs71469507	chr11:75873561-75873562	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
37	rs149585849	chr11:75873589-75873590	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
38	rs190357170	chr11:75873594-75873595	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
39	rs566229914	chr11:75873595-75873596	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
40	rs527258583	chr11:75873654-75873655	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs547451654	chr11:75873661-75873662	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs571152232	chr11:75873697-75873698	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs539792153	chr11:75873772-75873773	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs556819862	chr11:75873773-75873774	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs370828485	chr11:75873775-75873776	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs78668216	chr11:75873779-75873780	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs555417797	chr11:75873783-75873784	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs7933105	chr11:75873793-75873794	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs148757739	chr11:75873817-75873818	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs34894218	chr11:75873818-75873819	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
Breast cancer	21858162	CNVD
Ovarian cancer	21240255	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1464 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:75833400-75872800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr11:75865000-75876000	Weak transcription	Spleen	Spleen
3	chr11:75867800-75875200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
4	chr11:75869200-75874400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr11:75869600-75873000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr11:75870400-75874400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr11:75870400-75874600	Enhancers	Fetal Muscle Leg	muscle
8	chr11:75870600-75873800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr11:75871000-75873600	Enhancers	Fetal Brain Male	brain
10	chr11:75871400-75873400	Enhancers	Fetal Lung	lung
11	chr11:75871600-75873800	Enhancers	Fetal Heart	heart
12	chr11:75871800-75873000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr11:75871800-75874400	Enhancers	Placenta	Placenta
14	chr11:75872000-75873800	Enhancers	Left Ventricle	heart
15	chr11:75872200-75873200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr11:75872400-75872800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr11:75872400-75872800	Active TSS	Ovary	ovary
18	chr11:75872400-75872800	Flanking Active TSS	Right Atrium	heart
19	chr11:75872400-75872800	Active TSS	Right Ventricle	heart
20	chr11:75872400-75872800	Weak transcription	K562	blood
21	chr11:75872400-75873200	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr11:75872400-75873800	Enhancers	Lung	lung
23	chr11:75872400-75874000	Enhancers	Fetal Stomach	stomach
24	chr11:75872600-75872800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr11:75872600-75872800	Enhancers	Brain Hippocampus Middle	brain
26	chr11:75872600-75872800	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
27	chr11:75872600-75873000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr11:75872600-75873000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr11:75872600-75873000	Flanking Active TSS	Brain Germinal Matrix	brain
30	chr11:75872600-75873000	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr11:75872600-75873000	Flanking Active TSS	Fetal Brain Female	brain
32	chr11:75872600-75873000	Weak transcription	Pancreas	Pancrea
33	chr11:75872600-75873000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
34	chr11:75872600-75873000	Flanking Bivalent TSS/Enh	HepG2	liver
35	chr11:75872600-75873200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
36	chr11:75872600-75873400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
37	chr11:75872600-75874000	Enhancers	Fetal Intestine Large	intestine
38	chr11:75872600-75874800	Enhancers	Adipose Nuclei	Adipose
39	chr11:75872800-75873000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
40	chr11:75872800-75873000	Flanking Active TSS	Right Ventricle	heart
41	chr11:75872800-75873200	Enhancers	Ovary	ovary
42	chr11:75872800-75873400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr11:75872800-75873600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr11:75872800-75873600	Enhancers	Right Atrium	heart
45	chr11:75872800-75873600	Bivalent Enhancer	Stomach Smooth Muscle	stomach
46	chr11:75872800-75873800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr11:75872800-75873800	Enhancers	Fetal Intestine Small	intestine
48	chr11:75872800-75874600	Enhancers	K562	blood
49	chr11:75873000-75873200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr11:75873000-75873400	Enhancers	Brain Germinal Matrix	brain

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