Variant report

Variant	esv2757437
Chromosome Location	chr11:35067482-35238578
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4562)
CpG islands
(count:2200)
Chromatin interactive
region (count:98)
LncRNA
region (count:40)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:4562 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:35085029-35085388	K562	blood:	n/a	n/a
2	ARID3A	chr11:35212245-35212521	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:35194753-35195096	HepG2	liver:	n/a	n/a
4	ATF1	chr11:35166888-35167161	K562	blood:	n/a	n/a
5	ATF1	chr11:35164287-35164318	K562	blood:	n/a	n/a
6	ATF1	chr11:35088676-35088928	K562	blood:	n/a	n/a
7	ATF1	chr11:35168376-35168687	K562	blood:	n/a	n/a
8	ATF1	chr11:35132632-35132924	K562	blood:	n/a	n/a
9	ATF1	chr11:35069966-35070150	K562	blood:	n/a	n/a
10	ATF1	chr11:35122859-35123088	K562	blood:	n/a	n/a
11	ATF1	chr11:35120645-35121044	K562	blood:	n/a	n/a
12	ATF1	chr11:35084885-35085469	K562	blood:	n/a	n/a
13	ATF1	chr11:35162652-35162835	K562	blood:	n/a	n/a
14	ATF1	chr11:35104027-35104396	K562	blood:	n/a	n/a
15	ATF1	chr11:35125408-35125579	K562	blood:	n/a	n/a
16	ATF1	chr11:35099273-35099414	K562	blood:	n/a	n/a
17	ATF1	chr11:35133237-35133513	K562	blood:	n/a	n/a
18	ATF1	chr11:35072155-35072504	K562	blood:	n/a	n/a
19	ATF1	chr11:35182060-35182303	K562	blood:	n/a	n/a
20	ATF1	chr11:35079662-35080134	K562	blood:	n/a	n/a
21	ATF2	chr11:35111140-35111947	GM12878	blood:	n/a	n/a
22	ATF2	chr11:35140337-35140923	GM12878	blood:	n/a	n/a
23	ATF2	chr11:35098997-35100135	GM12878	blood:	n/a	n/a
24	ATF2	chr11:35187310-35187972	GM12878	blood:	n/a	n/a
25	ATF2	chr11:35104643-35105435	GM12878	blood:	n/a	n/a
26	ATF2	chr11:35167420-35168628	GM12878	blood:	n/a	n/a
27	ATF2	chr11:35165624-35166332	GM12878	blood:	n/a	n/a
28	ATF2	chr11:35166448-35167418	GM12878	blood:	n/a	n/a
29	ATF2	chr11:35109062-35110065	GM12878	blood:	n/a	n/a
30	ATF2	chr11:35148675-35149703	GM12878	blood:	n/a	n/a
31	ATF2	chr11:35147745-35149600	GM12878	blood:	n/a	n/a
32	ATF2	chr11:35088556-35089100	GM12878	blood:	n/a	n/a
33	ATF2	chr11:35147513-35148569	GM12878	blood:	n/a	n/a
34	ATF2	chr11:35143863-35144425	GM12878	blood:	n/a	n/a
35	ATF2	chr11:35166629-35167313	GM12878	blood:	n/a	n/a
36	ATF2	chr11:35088511-35089104	GM12878	blood:	n/a	n/a
37	ATF2	chr11:35165372-35166426	GM12878	blood:	n/a	n/a
38	ATF2	chr11:35187309-35188167	GM12878	blood:	n/a	n/a
39	ATF2	chr11:35109087-35109714	GM12878	blood:	n/a	n/a
40	ATF2	chr11:35208765-35209181	GM12878	blood:	n/a	n/a
41	ATF2	chr11:35103848-35104479	GM12878	blood:	n/a	n/a
42	ATF2	chr11:35104602-35105713	GM12878	blood:	n/a	n/a
43	ATF2	chr11:35167580-35168640	GM12878	blood:	n/a	n/a
44	ATF2	chr11:35152590-35153181	GM12878	blood:	n/a	n/a
45	ATF2	chr11:35072059-35072617	GM12878	blood:	n/a	n/a
46	ATF2	chr11:35140329-35140826	GM12878	blood:	n/a	n/a
47	ATF2	chr11:35099013-35100141	GM12878	blood:	n/a	n/a
48	ATF2	chr11:35071638-35072445	GM12878	blood:	n/a	n/a
49	ATF2	chr11:35111179-35111661	GM12878	blood:	n/a	n/a
50	ATF2	chr11:35104016-35104542	GM12878	blood:	n/a	n/a

(count:2200 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:35188437-35188487	AG10803	skin:	n/a
2	chr11:35161900-35161950	A549	lung:	n/a
3	chr11:35160892-35160942	HAEpiC	amniotic membrane:	n/a
4	chr11:35160571-35160621	ECC-1	luminal epithelium:	n/a
5	chr11:35188437-35188487	AG10803	skin:	n/a
6	chr11:35161900-35161950	A549	lung:	n/a
7	chr11:35160892-35160942	HAEpiC	amniotic membrane:	n/a
8	chr11:35160571-35160621	ECC-1	luminal epithelium:	n/a
9	chr11:35159087-35159137	SK-N-SH_RA	brain:	n/a
10	chr11:35167041-35167091	HMEC	breast:	n/a
11	chr11:35138084-35138134	MCF-7	breast:	n/a
12	chr11:35161229-35161279	NT2-D1	testis:	n/a
13	chr11:35160843-35160893	Hela-S3	cervix:	n/a
14	chr11:35160330-35160380	HCT-116	colon:	n/a
15	chr11:35072710-35072760	HL-60	blood:	n/a
16	chr11:35133274-35133324	NHBE	bronchial:	n/a
17	chr11:35161183-35161233	T-47D	breast:	n/a
18	chr11:35161183-35161233	AG10803	skin:	n/a
19	chr11:35186440-35186490	RPTEC	kidney:	n/a
20	chr11:35138084-35138134	HEEpiC	esophagus:	n/a
21	chr11:35105199-35105249	HCPEpiC	choroid plexus:	n/a
22	chr11:35161345-35161395	RPTEC	kidney:	n/a
23	chr11:35229448-35229498	BE2_C	brain:	n/a
24	chr11:35158283-35158333	PANC-1	pancreas:	n/a
25	chr11:35164485-35164535	NB4	blood:	n/a
26	chr11:35161229-35161279	NHBE	bronchial:	n/a
27	chr11:35160400-35160450	GM06990	blood:	n/a
28	chr11:35160571-35160621	Hepatocyte	liver:	n/a
29	chr11:35195513-35195563	HRCEpiC	kidney:	n/a
30	chr11:35173592-35173642	ECC-1	luminal epithelium:	n/a
31	chr11:35160571-35160621	HEEpiC	esophagus:	n/a
32	chr11:35195513-35195563	Hela-S3	cervix:	n/a
33	chr11:35229448-35229498	HRPEpiC	eye:	n/a
34	chr11:35158283-35158333	HCT-116	colon:	n/a
35	chr11:35160571-35160621	IMR90	lung:	fetal
36	chr11:35201133-35201183	NH-A	brain:	n/a
37	chr11:35160400-35160450	ovcar-3	ovarian:	n/a
38	chr11:35229448-35229498	AG10803	skin:	n/a
39	chr11:35229448-35229498	Hela-S3	cervix:	n/a
40	chr11:35159087-35159137	Hela-S3	cervix:	n/a
41	chr11:35188437-35188487	NT2-D1	testis:	n/a
42	chr11:35160843-35160893	Jurkat	blood:	n/a
43	chr11:35188437-35188487	SK-N-MC	brain:	n/a
44	chr11:35188437-35188487	GM06990	blood:	n/a
45	chr11:35159382-35159432	RPTEC	kidney:	n/a
46	chr11:35086165-35086215	AG04449	skin:	fetal
47	chr11:35160498-35160548	PFSK-1	brain:	n/a
48	chr11:35160571-35160621	MCF10A-Er-Src	breast:	n/a
49	chr11:35158283-35158333	HCF	heart:	n/a
50	chr11:35160892-35160942	AG09309	skin:	n/a

(count:98 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:35143665..35146006-chr11:35146722..35148953,2	MCF-7	breast:
2	chr11:35234685..35237294-chr11:35237547..35239345,2	MCF-7	breast:
3	chr11:35186531..35188215-chr11:35413426..35415708,2	MCF-7	breast:
4	chr11:35188706..35190323-chr11:35204261..35206876,2	K562	blood:
5	chr11:35172301..35174738-chr11:35189496..35192114,2	MCF-7	breast:
6	chr11:35086278..35088027-chr11:35090428..35092324,3	K562	blood:
7	chr11:35119495..35120096-chr11:35412276..35412995,2	MCF-7	breast:
8	chr11:35163163..35167316-chr11:35171190..35174236,4	K562	blood:
9	chr11:35110163..35112423-chr11:35159701..35161676,2	MCF-7	breast:
10	chr11:35097231..35099674-chr11:35101240..35103980,3	K562	blood:
11	chr11:35123473..35125204-chr11:35129634..35132229,2	MCF-7	breast:
12	chr11:35160960..35162794-chr11:35186248..35188654,2	MCF-7	breast:
13	chr11:35119423..35121112-chr11:35124669..35126752,2	MCF-7	breast:
14	chr11:35198118..35199850-chr11:35204330..35207060,2	K562	blood:
15	chr11:35123473..35125204-chr11:35129634..35132229,2	MCF-7	breast:
16	chr11:35188706..35190323-chr11:35204261..35206876,2	K562	blood:
17	chr11:35163163..35167316-chr11:35171190..35174236,4	K562	blood:
18	chr11:35122584..35124925-chr11:35126765..35129371,2	MCF-7	breast:
19	chr11:35170246..35172817-chr11:35174979..35176507,2	MCF-7	breast:
20	chr11:35086278..35088027-chr11:35090428..35092324,3	K562	blood:
21	chr11:35172301..35174738-chr11:35189496..35192114,2	MCF-7	breast:
22	chr11:35227871..35230257-chr11:35238452..35241345,2	MCF-7	breast:
23	chr11:35169325..35170963-chr11:35175287..35177044,2	K562	blood:
24	chr11:35193443..35196303-chr11:35198924..35201669,2	MCF-7	breast:
25	chr11:35123609..35125478-chr11:35160638..35163395,2	MCF-7	breast:
26	chr11:35087035..35089860-chr11:35091064..35093898,2	MCF-7	breast:
27	chr11:35137747..35140053-chr11:35157394..35160229,2	MCF-7	breast:
28	chr11:35155392..35158105-chr11:35159031..35160697,2	MCF-7	breast:
29	chr11:35199491..35202638-chr11:35207456..35210593,3	MCF-7	breast:
30	chr1:89149746..89150285-chr11:35160701..35161440,2	HCT-116	colon:
31	chr11:35160366..35160877-chr15:44069390..44069929,2	Hela-S3	cervix:
32	chr1:11968192..11969146-chr11:35160267..35160843,2	Hela-S3	cervix:
33	chr11:35187046..35189640-chr11:35384110..35385949,2	MCF-7	breast:
34	chr11:35169325..35170963-chr11:35175287..35177044,2	K562	blood:
35	chr11:34938093..34939698-chr11:35166380..35168722,2	MCF-7	breast:
36	chr1:155579443..155580336-chr11:35160348..35160978,2	NB4	blood:
37	chr11:35132300..35135003-chr11:35146023..35147940,2	MCF-7	breast:
38	chr11:35193443..35196303-chr11:35198924..35201669,2	MCF-7	breast:
39	chr11:35208296..35211320-chr11:35214358..35217497,3	K562	blood:
40	chr1:207503349..207504173-chr11:35160887..35161695,2	Hela-S3	cervix:
41	chr11:35083507..35086389-chr11:35411165..35412873,2	MCF-7	breast:
42	chr11:35160535..35161197-chr7:100033923..100034574,2	Hela-S3	cervix:
43	chr11:35183121..35185456-chr11:35188061..35190243,2	MCF-7	breast:
44	chr11:35129946..35132170-chr11:35133262..35135380,2	K562	blood:
45	chr11:35118109..35120819-chr11:35160068..35162189,2	MCF-7	breast:
46	chr11:35160364..35160882-chr15:75932271..75932998,2	Hela-S3	cervix:
47	chr11:35161963..35164830-chr11:35383993..35385550,2	MCF-7	breast:
48	chr11:35160324..35161311-chr3:14444116..14444878,2	Hela-S3	cervix:
49	chr11:35097231..35099674-chr11:35101240..35103980,3	K562	blood:
50	chr11:35026967..35028548-chr11:35162664..35165084,2	MCF-7	breast:

(count:40 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD44-4	chr11:35124735-35124991	NONHSAT018773
2	lnc-APIP-1	chr11:35086667-35086860	NONHSAT018769
3	lnc-PDHX-3	chr11:35140600-35142723	NONHSAT018772
4	lnc-PDHX-5	chr11:35222691-35222742	NONHSAT018781
5	lnc-PDHX-5	chr11:35226059-35226358	NONHSAT018779
6	lnc-PDHX-5	chr11:35229652-35229711	NONHSAT018783
7	lnc-PDHX-5	chr11:35211473-35211612	NONHSAT018779
8	lnc-PDHX-3	chr11:35119065-35120242	NONHSAT018772
9	lnc-CD44-3	chr11:35132621-35132927	NONHSAT018774
10	lnc-PDHX-5	chr11:35223215-35223334	NONHSAT018781
11	lnc-SLC1A2-2	chr11:35159245-35159273	ENSG00000255521.1
12	lnc-SLC1A2-2	chr11:35157781-35158173	ENSG00000255521.1
13	lnc-CD44-5	chr11:35103203-35103622	NONHSAT018771
14	lnc-APIP-1	chr11:35088226-35088723	NONHSAT018769
15	lnc-SLC1A2-1	chr11:35236378-35236532	ENSG00000255443.1
16	lnc-APIP-1	chr11:35095464-35095505	XLOC_009415
17	lnc-APIP-1	chr11:35080723-35081531	NONHSAT018769
18	lnc-SLC1A2-2	chr11:35150431-35150467	XLOC_009416
19	lnc-PDHX-5	chr11:35232793-35232996	NONHSAT018782
20	lnc-PDHX-3	chr11:35109985-35110151	NONHSAT018768
21	lnc-SLC1A2-1	chr11:35231890-35232321	ENSG00000255443.1
22	lnc-SLC1A2-2	chr11:35154202-35154687	ENSG00000255521.1
23	lnc-PDHX-3	chr11:35119168-35119365	NONHSAT018768
24	lnc-PDHX-5	chr11:35236399-35236461	NONHSAT018782
25	lnc-SLC1A2-2	chr11:35159245-35159579	ENSG00000255521.1
26	lnc-SLC1A2-2	chr11:35157893-35158173	ENSG00000255521.1
27	lnc-PDHX-3	chr11:35107760-35107870	NONHSAT018772
28	lnc-PDHX-5	chr11:35223168-35223334	NONHSAT018782
29	lnc-PDHX-3	chr11:35108965-35110133	NONHSAT018772
30	lnc-PDHX-4	chr11:35218709-35219340	NONHSAT018780
31	lnc-SLC1A2-2	chr11:35157893-35158084	XLOC_009416
32	lnc-PDHX-3	chr11:35071626-35071672	NONHSAT018768
33	lnc-PDHX-1	chr11:35235151-35235554	ENSG00000251194
34	lnc-PDHX-3	chr11:35112276-35112331	NONHSAT018772
35	lnc-PDHX-5	chr11:35226059-35226187	NONHSAT018781
36	lnc-PDHX-1	chr11:35234097-35234396	ENSG00000251194
37	lnc-PDHX-5	chr11:35227332-35227594	NONHSAT018781
38	lnc-PDHX-5	chr11:35227262-35227790	NONHSAT018783
39	lnc-APIP-1	chr11:35086673-35086860	XLOC_009415
40	lnc-PDHX-4	chr11:35219416-35220102	NONHSAT018780

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CD44	hsa-miR-373-3p	chr11:35211492-35211514
2	CD44	hsa-miR-520c-3p	chr11:35211491-35211514

Variant related genes	Relation type
ENSG00000269766	TF binding region
CD44	TF binding region
ENSG00000251194	TF binding region
ENSG00000255443	TF binding region
ENSG00000255521	TF binding region
ENSG00000269766	CpG island
CD44	CpG island
ENSG00000251194	CpG island
ENSG00000255443	CpG island
ENSG00000255521	CpG island
ENSG00000109089	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000128886	chromatin interactions
ENSG00000269766	chromatin interactions
ENSG00000120129	chromatin interactions
ENSG00000232519	chromatin interactions
ENSG00000143549	chromatin interactions
ENSG00000125459	chromatin interactions
ENSG00000271853	chromatin interactions
ENSG00000177971	chromatin interactions
ENSG00000131389	chromatin interactions
ENSG00000269946	chromatin interactions
ENSG00000272030	chromatin interactions
ENSG00000065243	chromatin interactions
ENSG00000160741	chromatin interactions
ENSG00000026508	chromatin interactions
ENSG00000255443	chromatin interactions
ENSG00000255521	chromatin interactions
ENSG00000160813	chromatin interactions
ENSG00000110435	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000197837	chromatin interactions
POU2F1	miRNA target sites
GLCE	miRNA target sites
GANAB	miRNA target sites
CUEDC2	miRNA target sites

Extended variants
information (count: 6917 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:6917 , 50 per page) page: 1 2 3 4 5 6 7 ... 139

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2785156	chr11:35067482-35067483	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537178507	chr11:35067486-35067487	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs188065387	chr11:35067495-35067496	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs181013623	chr11:35067502-35067503	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs537416208	chr11:35067503-35067504	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs375471337	chr11:35067587-35067588	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs75562784	chr11:35067605-35067606	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs567484594	chr11:35067704-35067705	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs534562851	chr11:35067724-35067725	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs554316407	chr11:35067725-35067726	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs568405926	chr11:35067785-35067786	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs537384984	chr11:35067789-35067790	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs557113486	chr11:35067803-35067804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs576998646	chr11:35067834-35067835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs146675308	chr11:35067877-35067878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs534763285	chr11:35067887-35067888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs367924438	chr11:35067896-35067897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs370806116	chr11:35067905-35067906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186217079	chr11:35067918-35067919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs567351953	chr11:35067962-35067963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs562103456	chr11:35067976-35067977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79162897	chr11:35067998-35067999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs2553787	chr11:35068016-35068017	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs139068933	chr11:35068052-35068053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs368505324	chr11:35068087-35068088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs78098648	chr11:35068140-35068141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs142573860	chr11:35068141-35068142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs565764063	chr11:35068168-35068169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs528216527	chr11:35068191-35068192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs547770271	chr11:35068203-35068204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs666197	chr11:35068208-35068209	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs548342983	chr11:35068269-35068270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs34156441	chr11:35068276-35068277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs35049718	chr11:35068307-35068308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs397698162	chr11:35068315-35068316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150948247	chr11:35068350-35068351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs571063958	chr11:35068351-35068352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539972710	chr11:35068364-35068365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs553336187	chr11:35068369-35068370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs573276840	chr11:35068390-35068391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs535609063	chr11:35068391-35068392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375585542	chr11:35068395-35068396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs542326485	chr11:35068412-35068413	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs555775362	chr11:35068422-35068423	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs575681675	chr11:35068438-35068439	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs544632476	chr11:35068558-35068559	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs563528273	chr11:35068595-35068596	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs2785155	chr11:35068606-35068607	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs545971045	chr11:35068610-35068611	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs140834434	chr11:35068617-35068618	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Lung squamous cell carcinoma	20842114	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:5855 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:35061000-35071800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr11:35061800-35068400	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr11:35061800-35069400	Enhancers	Primary hematopoietic stem cells	blood
4	chr11:35061800-35072800	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr11:35062600-35069800	Weak transcription	Placenta	Placenta
6	chr11:35062600-35070200	Weak transcription	Stomach Mucosa	stomach
7	chr11:35062600-35070400	Weak transcription	Esophagus	oesophagus
8	chr11:35062800-35071800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr11:35062800-35073600	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr11:35063000-35071600	Weak transcription	K562	blood
11	chr11:35063200-35069800	Enhancers	Fetal Thymus	thymus
12	chr11:35063800-35068600	Weak transcription	Lung	lung
13	chr11:35064000-35067600	Enhancers	Fetal Stomach	stomach
14	chr11:35064000-35077200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr11:35064400-35072000	Weak transcription	HSMMtube	muscle
16	chr11:35065000-35070400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr11:35065200-35071000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
18	chr11:35065200-35073200	Enhancers	Primary T cells fromperipheralblood	blood
19	chr11:35065400-35069600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
20	chr11:35065400-35072600	Enhancers	Primary B cells from peripheral blood	blood
21	chr11:35065600-35067600	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr11:35065600-35068000	Enhancers	Duodenum Mucosa	Duodenum
23	chr11:35065600-35069200	Enhancers	Thymus	Thymus
24	chr11:35065600-35073200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr11:35065800-35067800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
26	chr11:35066000-35068800	Weak transcription	Colon Smooth Muscle	Colon
27	chr11:35066200-35067800	Enhancers	Fetal Intestine Large	intestine
28	chr11:35066200-35067800	Enhancers	Fetal Intestine Small	intestine
29	chr11:35066200-35067800	Enhancers	HepG2	liver
30	chr11:35066400-35067600	Enhancers	GM12878-XiMat	blood
31	chr11:35066400-35068400	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr11:35066400-35070400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr11:35066400-35070400	Weak transcription	Adipose Nuclei	Adipose
34	chr11:35066600-35067600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
35	chr11:35066800-35067600	Enhancers	Fetal Lung	lung
36	chr11:35066800-35067600	Enhancers	A549	lung
37	chr11:35066800-35070400	Weak transcription	Spleen	Spleen
38	chr11:35067000-35067600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
39	chr11:35067000-35071600	Weak transcription	Rectal Smooth Muscle	rectum
40	chr11:35067200-35067600	Enhancers	Primary T cells from cord blood	blood
41	chr11:35067200-35067600	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr11:35067200-35068400	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr11:35067200-35068400	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr11:35067200-35070400	Weak transcription	Fetal Muscle Leg	muscle
45	chr11:35067200-35070400	Weak transcription	Pancreas	Pancrea
46	chr11:35067200-35071600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr11:35067400-35067600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr11:35067400-35067800	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr11:35067400-35068400	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr11:35067400-35068600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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