Variant report

Variant	nsv1015075
Chromosome Location	chr3:21791806-21809266
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:285)
CpG islands
(count:549)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:285 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:21792431-21793017	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr3:21792339-21792940	H1-hESC	embryonic stem cell:	n/a	n/a
3	CHD1	chr3:21792005-21792065	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD1	chr3:21792482-21792673	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD2	chr3:21792301-21793038	H1-hESC	embryonic stem cell:	n/a	n/a
6	CREB1	chr3:21792463-21792984	H1-hESC	embryonic stem cell:	n/a	n/a
7	CREB1	chr3:21792360-21793085	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTBP2	chr3:21792388-21792991	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr3:21794440-21794590	HCT-116	colon:	n/a	n/a
10	CTCF	chr3:21794360-21794510	HRE	kidney:	n/a	n/a
11	CTCF	chr3:21794400-21794550	MCF-7	breast:	n/a	n/a
12	CTCF	chr3:21794400-21794550	AG09309	skin:	n/a	n/a
13	CTCF	chr3:21794360-21794510	GM12874	blood:	n/a	n/a
14	CTCF	chr3:21794380-21794530	BJ	skin:	n/a	n/a
15	CTCF	chr3:21794360-21794510	SAEC	small airway:	n/a	n/a
16	CTCF	chr3:21794340-21794490	SAEC	small airway:	n/a	n/a
17	CTCF	chr3:21794316-21794572	HUVEC	blood vessel:	n/a	n/a
18	CTCF	chr3:21794360-21794510	GM12875	blood:	n/a	n/a
19	CTCF	chr3:21794400-21794550	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr3:21794300-21794450	RPTEC	kidney:	n/a	n/a
21	CTCF	chr3:21794340-21794490	GM06990	blood:	n/a	n/a
22	CTCF	chr3:21794360-21794510	GM12873	blood:	n/a	n/a
23	CTCF	chr3:21794340-21794490	GM12871	blood:	n/a	n/a
24	CTCF	chr3:21794340-21794490	GM12867	blood:	n/a	n/a
25	CTCF	chr3:21794291-21794623	Medullo	brain:	n/a	n/a
26	CTCF	chr3:21794360-21794510	GM12868	blood:	n/a	n/a
27	CTCF	chr3:21793980-21794130	AG10803	skin:	n/a	n/a
28	CTCF	chr3:21794340-21794490	GM12874	blood:	n/a	n/a
29	CTCF	chr3:21794314-21794570	Lung_OC	lung:	n/a	n/a
30	CTCF	chr3:21794320-21794470	HA-sp	spinal cord:	n/a	n/a
31	CTCF	chr3:21794380-21794530	BE2_C	brain:	n/a	n/a
32	CTCF	chr3:21794360-21794510	HRPEpiC	eye:	n/a	n/a
33	CTCF	chr3:21794380-21794530	GM12864	blood:	n/a	n/a
34	CTCF	chr3:21794317-21794600	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr3:21794280-21794430	A549	lung:	n/a	n/a
36	CTCF	chr3:21794280-21794430	HCM	heart:	n/a	n/a
37	CTCF	chr3:21794360-21794510	RPTEC	kidney:	n/a	n/a
38	CTCF	chr3:21793500-21793650	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr3:21794317-21794560	ProgFib	skin:	n/a	n/a
40	CTCF	chr3:21794320-21794470	HepG2	liver:	n/a	n/a
41	CTCF	chr3:21794380-21794530	GM12865	blood:	n/a	n/a
42	CTCF	chr3:21794380-21794530	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr3:21794340-21794490	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr3:21794340-21794490	AG10803	skin:	n/a	n/a
45	CTCF	chr3:21794400-21794550	GM12864	blood:	n/a	n/a
46	CTCF	chr3:21794380-21794530	AG09319	gingival:	n/a	n/a
47	CTCF	chr3:21792520-21792670	HMEC	breast:	n/a	n/a
48	CTCF	chr3:21794340-21794490	NHLF	lung:	n/a	n/a
49	CTCF	chr3:21794360-21794510	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr3:21794247-21794629	GM12878	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:21792434-21792484	HEK293	kidney:	embryo
2	chr3:21792965-21793015	NHDF-neo	bronchial:	n/a
3	chr3:21792965-21793015	ovcar-3	ovarian:	n/a
4	chr3:21792684-21792734	CMK	blood:	n/a
5	chr3:21792991-21793041	PFSK-1	brain:	n/a
6	chr3:21792938-21792988	AG04450	lung:	fetal
7	chr3:21793557-21793607	BE2_C	brain:	n/a
8	chr3:21792684-21792734	HRCEpiC	kidney:	n/a
9	chr3:21792991-21793041	NHDF-neo	bronchial:	n/a
10	chr3:21793557-21793607	HL-60	blood:	n/a
11	chr3:21792965-21793015	HCPEpiC	choroid plexus:	n/a
12	chr3:21792543-21792593	ovcar-3	ovarian:	n/a
13	chr3:21792543-21792593	HRE	kidney:	n/a
14	chr3:21792543-21792593	Hepatocyte	liver:	n/a
15	chr3:21792938-21792988	GM12878	blood:	n/a
16	chr3:21792965-21793015	HEK293	kidney:	embryo
17	chr3:21792991-21793041	NT2-D1	testis:	n/a
18	chr3:21792684-21792734	Jurkat	blood:	n/a
19	chr3:21792248-21792298	GM12892	blood:	n/a
20	chr3:21792684-21792734	HCM	heart:	n/a
21	chr3:21792248-21792298	AG04450	lung:	fetal
22	chr3:21792434-21792484	HepG2	liver:	n/a
23	chr3:21792938-21792988	ECC-1	luminal epithelium:	n/a
24	chr3:21792965-21793015	A549	lung:	n/a
25	chr3:21792434-21792484	Caco-2	colon:	n/a
26	chr3:21792434-21792484	PrEC	prostate:	n/a
27	chr3:21792434-21792484	NB4	blood:	n/a
28	chr3:21792434-21792484	ProgFib	skin:	n/a
29	chr3:21793557-21793607	HIPEpiC	eye:	n/a
30	chr3:21792938-21792988	MCF-7	breast:	n/a
31	chr3:21792248-21792298	NHBE	bronchial:	n/a
32	chr3:21792434-21792484	GM12891	blood:	n/a
33	chr3:21792938-21792988	SAEC	small airway:	n/a
34	chr3:21792991-21793041	GM12892	blood:	n/a
35	chr3:21793557-21793607	Hela-S3	cervix:	n/a
36	chr3:21792543-21792593	NB4	blood:	n/a
37	chr3:21793557-21793607	ProgFib	skin:	n/a
38	chr3:21792991-21793041	HRPEpiC	eye:	n/a
39	chr3:21792434-21792484	T-47D	breast:	n/a
40	chr3:21792684-21792734	HCF	heart:	n/a
41	chr3:21792938-21792988	SK-N-SH	brain:	n/a
42	chr3:21792991-21793041	HEEpiC	esophagus:	n/a
43	chr3:21792248-21792298	GM19239	blood:	n/a
44	chr3:21792991-21793041	HAEpiC	amniotic membrane:	n/a
45	chr3:21792938-21792988	PrEC	prostate:	n/a
46	chr3:21792434-21792484	K562	blood:	n/a
47	chr3:21792434-21792484	HL-60	blood:	n/a
48	chr3:21792965-21793015	GM12891	blood:	n/a
49	chr3:21792248-21792298	HIPEpiC	eye:	n/a
50	chr3:21792684-21792734	HMEC	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:21793963..21794585-chr3:21876272..21877179,2	MCF-7	breast:
2	chr3:21794398..21795153-chr3:22159350..22159975,2	MCF-7	breast:
3	chr3:21793981..21794891-chr3:21935742..21936689,4	MCF-7	breast:

No data

Variant related genes	Relation type
ZNF385D	TF binding region
ZNF385D	CpG island

Extended variants
information (count: 581 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:581 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535150644	chr3:21791826-21791827	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs370416059	chr3:21791850-21791851	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566655078	chr3:21791881-21791882	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs137914055	chr3:21791888-21791889	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs4858014	chr3:21791930-21791931	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs571541854	chr3:21791962-21791963	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs73822048	chr3:21791975-21791976	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs112465001	chr3:21791981-21791982	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs78814729	chr3:21792017-21792018	Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs148256154	chr3:21792041-21792042	Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs181007254	chr3:21792089-21792090	Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564011408	chr3:21792113-21792114	Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs559562843	chr3:21792119-21792120	Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528236819	chr3:21792135-21792136	Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs149636790	chr3:21792164-21792165	Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs541807353	chr3:21792207-21792208	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185067629	chr3:21792215-21792216	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528908363	chr3:21792221-21792222	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs369736107	chr3:21792224-21792225	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561708876	chr3:21792229-21792230	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs550959363	chr3:21792233-21792234	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569558216	chr3:21792235-21792236	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533344460	chr3:21792255-21792256	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs572848497	chr3:21792268-21792269	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566621071	chr3:21792290-21792291	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs190216625	chr3:21792311-21792312	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555448344	chr3:21792330-21792331	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs7636784	chr3:21792363-21792364	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs182478819	chr3:21792377-21792378	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs187434095	chr3:21792452-21792453	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs374829726	chr3:21792456-21792457	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs7623075	chr3:21792485-21792486	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs545669986	chr3:21792496-21792497	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs558031434	chr3:21792502-21792503	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs573078415	chr3:21792508-21792509	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541564679	chr3:21792545-21792546	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs111278809	chr3:21792554-21792555	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs113632612	chr3:21792571-21792572	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs11541213	chr3:21792578-21792579	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs150791283	chr3:21792581-21792582	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs62236195	chr3:21792602-21792603	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs543869559	chr3:21792652-21792653	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs563028259	chr3:21792667-21792668	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs533725176	chr3:21792670-21792671	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs551787482	chr3:21792677-21792678	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs560270739	chr3:21792683-21792684	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs369498668	chr3:21792737-21792738	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs7623361	chr3:21792766-21792767	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs549036433	chr3:21792783-21792784	Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs567449441	chr3:21792806-21792807	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Melanoma	20688739	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:203 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:21786400-21793600	Active TSS	Aorta	Aorta
2	chr3:21788800-21793200	Active TSS	Duodenum Smooth Muscle	Duodenum
3	chr3:21789200-21793200	Active TSS	Fetal Brain Female	brain
4	chr3:21789400-21793200	Active TSS	NHDF-Ad	bronchial
5	chr3:21789600-21792600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr3:21789800-21793200	Active TSS	Stomach Smooth Muscle	stomach
7	chr3:21790000-21793400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr3:21790200-21792000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr3:21790200-21792200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr3:21790200-21792800	Active TSS	Fetal Muscle Leg	muscle
11	chr3:21790200-21793200	Active TSS	Right Atrium	heart
12	chr3:21790200-21793200	Active TSS	Right Ventricle	heart
13	chr3:21790400-21792800	Active TSS	NHLF	lung
14	chr3:21790400-21793200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr3:21790400-21793200	Active TSS	Left Ventricle	heart
16	chr3:21790600-21793200	Active TSS	Breast Myoepithelial Primary Cells	Breast
17	chr3:21790600-21793200	Active TSS	Fetal Muscle Trunk	muscle
18	chr3:21790600-21793200	Active TSS	Fetal Stomach	stomach
19	chr3:21790800-21793200	Active TSS	Brain Germinal Matrix	brain
20	chr3:21790800-21793200	Active TSS	HMEC	breast
21	chr3:21790800-21793400	Active TSS	Fetal Brain Male	brain
22	chr3:21790800-21793400	Active TSS	Fetal Kidney	kidney
23	chr3:21791000-21792800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr3:21791000-21793000	Active TSS	Rectal Smooth Muscle	rectum
25	chr3:21791200-21792000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr3:21791200-21792400	Flanking Active TSS	NH-A	brain
27	chr3:21791400-21792200	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
28	chr3:21791400-21792200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
29	chr3:21791400-21792400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
30	chr3:21791400-21792400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr3:21791400-21792400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr3:21791400-21793200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr3:21791400-21793400	Active TSS	H9 Cell Line	embryonic stem cell
34	chr3:21791600-21792000	Flanking Active TSS	H1 Cell Line	embryonic stem cell
35	chr3:21791600-21792000	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
36	chr3:21791600-21792000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
37	chr3:21791600-21792000	Flanking Active TSS	Brain Anterior Caudate	brain
38	chr3:21791600-21792000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
39	chr3:21791600-21792000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr3:21791600-21792000	Bivalent/Poised TSS	Fetal Lung	lung
41	chr3:21791600-21792000	Flanking Active TSS	Ovary	ovary
42	chr3:21791600-21792000	Flanking Active TSS	HSMM	muscle
43	chr3:21791600-21792200	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr3:21791600-21792200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
45	chr3:21791600-21792200	Flanking Active TSS	Brain Angular Gyrus	brain
46	chr3:21791600-21792400	Flanking Active TSS	HSMMtube	muscle
47	chr3:21791600-21792600	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr3:21791600-21792600	Active TSS	Colon Smooth Muscle	Colon
49	chr3:21791600-21792600	Enhancers	Gastric	stomach
50	chr3:21791600-21792800	Active TSS	Esophagus	oesophagus

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