Variant report

Variant	esv3325944
Chromosome Location	chr3:178788483-178791031
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:522)
CpG islands
(count:734)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:522 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:178789396-178790175	GM12878	blood:	n/a	n/a
2	BACH1	chr3:178788995-178789425	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr3:178789634-178789859	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr3:178788894-178789282	GM12878	blood:	n/a	n/a
5	BCL11A	chr3:178788900-178789343	GM12878	blood:	n/a	chr3:178789166-178789175
6	BCL3	chr3:178788914-178789331	GM12878	blood:	n/a	chr3:178789166-178789175
7	BCLAF1	chr3:178788809-178790206	GM12878	blood:	n/a	chr3:178790047-178790056 chr3:178789505-178789518 chr3:178789508-178789521 chr3:178789504-178789517 chr3:178789761-178789774 chr3:178789166-178789175 chr3:178789585-178789594 chr3:178789501-178789514
8	BCLAF1	chr3:178789346-178790369	GM12878	blood:	n/a	chr3:178790047-178790056 chr3:178789505-178789518 chr3:178789508-178789521 chr3:178789504-178789517 chr3:178789761-178789774 chr3:178789585-178789594 chr3:178789501-178789514
9	BCLAF1	chr3:178788883-178789316	GM12878	blood:	n/a	chr3:178789166-178789175
10	BHLHE40	chr3:178788933-178789919	GM12878	blood:	n/a	chr3:178789680-178789696 chr3:178789719-178789735
11	BHLHE40	chr3:178788690-178789918	K562	blood:	n/a	chr3:178789680-178789696 chr3:178789719-178789735
12	BRCA1	chr3:178789470-178789695	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr3:178789286-178789328	HepG2	liver:	n/a	n/a
14	CBX3	chr3:178788887-178789407	K562	blood:	n/a	n/a
15	CBX3	chr3:178789422-178789978	K562	blood:	n/a	n/a
16	CBX3	chr3:178789993-178790415	K562	blood:	n/a	n/a
17	CCNT2	chr3:178789177-178789865	K562	blood:	n/a	n/a
18	CEBPB	chr3:178789160-178790088	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr3:178789595-178789988	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPD	chr3:178789561-178789840	HepG2	liver:	n/a	n/a
21	CEBPD	chr3:178789601-178789801	HepG2	liver:	n/a	n/a
22	CHD1	chr3:178788781-178789772	GM12878	blood:	n/a	n/a
23	CHD2	chr3:178789064-178790020	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr3:178789486-178789792	K562	blood:	n/a	n/a
25	CHD2	chr3:178789024-178789976	GM12878	blood:	n/a	n/a
26	CHD2	chr3:178790138-178790147	HepG2	liver:	n/a	n/a
27	CHD2	chr3:178789566-178789725	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr3:178789494-178789734	HepG2	liver:	n/a	n/a
29	CREB1	chr3:178789389-178789809	A549	lung:	n/a	n/a
30	CTBP2	chr3:178789007-178790005	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr3:178789084-178789240	GM12878	blood:	n/a	n/a
32	CTCF	chr3:178789560-178789710	AG04449	skin:	n/a	n/a
33	CTCF	chr3:178789639-178790146	GM12878	blood:	n/a	chr3:178789721-178789734
34	CTCF	chr3:178789600-178789750	GM12868	blood:	n/a	chr3:178789721-178789734
35	CTCF	chr3:178789109-178789220	MCF-7	breast:	n/a	n/a
36	CTCF	chr3:178789643-178789723	GM19239	blood:	n/a	n/a
37	CTCF	chr3:178789860-178790010	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr3:178789606-178789761	MCF-7	breast:	n/a	chr3:178789721-178789734
39	CTCF	chr3:178789620-178789770	WERI-Rb-1	eye:	n/a	chr3:178789721-178789734
40	CTCF	chr3:178789565-178789701	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr3:178789840-178789990	GM12871	blood:	n/a	n/a
42	CTCF	chr3:178789631-178789685	NHEK	skin:	n/a	n/a
43	CTCF	chr3:178789679-178789684	ProgFib	skin:	n/a	n/a
44	CTCF	chr3:178789680-178789830	SK-N-SH_RA	brain:	n/a	chr3:178789721-178789734
45	CTCF	chr3:178789960-178790110	AG10803	skin:	n/a	n/a
46	CTCF	chr3:178789620-178789770	MCF-7	breast:	n/a	chr3:178789721-178789734
47	CTCF	chr3:178789600-178789750	SK-N-SH_RA	brain:	n/a	chr3:178789721-178789734
48	CTCF	chr3:178789320-178789470	GM12874	blood:	n/a	n/a
49	CTCF	chr3:178789614-178789697	GM12892	blood:	n/a	n/a
50	CTCF	chr3:178789654-178789744	K562	blood:	n/a	chr3:178789721-178789734

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:178789599-178789649	GM06990	blood:	n/a
2	chr3:178789707-178789757	SK-N-SH_RA	brain:	n/a
3	chr3:178789599-178789649	GM06990	blood:	n/a
4	chr3:178789707-178789757	SK-N-SH_RA	brain:	n/a
5	chr3:178789534-178789584	SAEC	small airway:	n/a
6	chr3:178789826-178789876	IMR90	lung:	fetal
7	chr3:178789599-178789649	NB4	blood:	n/a
8	chr3:178789528-178789578	HUVEC	blood vessel:	n/a
9	chr3:178789784-178789834	GM12892	blood:	n/a
10	chr3:178789707-178789757	NHBE	bronchial:	n/a
11	chr3:178789438-178789488	ovcar-3	ovarian:	n/a
12	chr3:178789612-178789662	PFSK-1	brain:	n/a
13	chr3:178790077-178790127	ECC-1	luminal epithelium:	n/a
14	chr3:178789612-178789662	ECC-1	luminal epithelium:	n/a
15	chr3:178790077-178790127	NH-A	brain:	n/a
16	chr3:178789848-178789898	AG10803	skin:	n/a
17	chr3:178789707-178789757	HEEpiC	esophagus:	n/a
18	chr3:178789823-178789873	GM06990	blood:	n/a
19	chr3:178789612-178789662	AoSMC	blood vessel:	n/a
20	chr3:178790077-178790127	MCF-7	breast:	n/a
21	chr3:178789438-178789488	HCF	heart:	n/a
22	chr3:178789226-178789276	ProgFib	skin:	n/a
23	chr3:178789599-178789649	AG09309	skin:	n/a
24	chr3:178789848-178789898	HCT-116	colon:	n/a
25	chr3:178789784-178789834	HRCEpiC	kidney:	n/a
26	chr3:178789534-178789584	HAEpiC	amniotic membrane:	n/a
27	chr3:178789823-178789873	CMK	blood:	n/a
28	chr3:178789826-178789876	GM06990	blood:	n/a
29	chr3:178789226-178789276	HCPEpiC	choroid plexus:	n/a
30	chr3:178790077-178790127	AG04450	lung:	fetal
31	chr3:178789826-178789876	Jurkat	blood:	n/a
32	chr3:178789438-178789488	Hepatocyte	liver:	n/a
33	chr3:178789612-178789662	K562	blood:	n/a
34	chr3:178789823-178789873	A549	lung:	n/a
35	chr3:178789823-178789873	HMEC	breast:	n/a
36	chr3:178789528-178789578	H1-hESC	embryonic stem cell:	embryo
37	chr3:178789823-178789873	HUVEC	blood vessel:	n/a
38	chr3:178789826-178789876	Caco-2	colon:	n/a
39	chr3:178789438-178789488	Hela-S3	cervix:	n/a
40	chr3:178790077-178790127	GM19239	blood:	n/a
41	chr3:178789612-178789662	Jurkat	blood:	n/a
42	chr3:178790077-178790127	HCT-116	colon:	n/a
43	chr3:178789528-178789578	BJ	skin:	n/a
44	chr3:178789823-178789873	MCF-7	breast:	n/a
45	chr3:178789848-178789898	SK-N-MC	brain:	n/a
46	chr3:178789848-178789898	BJ	skin:	n/a
47	chr3:178789599-178789649	LNCaP	prostate:	n/a
48	chr3:178789438-178789488	ProgFib	skin:	n/a
49	chr3:178789612-178789662	PrEC	prostate:	n/a
50	chr3:178789599-178789649	NH-A	brain:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:178788554..178791044-chr3:178814072..178816691,3	MCF-7	breast:
2	chr3:178788447..178791036-chr3:178864497..178866649,2	MCF-7	breast:
3	chr3:178786925..178789099-chr3:178864297..178866724,2	K562	blood:
4	chr3:178788412..178790187-chr3:179039067..179041157,2	MCF-7	breast:
5	chr3:178787758..178789707-chr3:178977770..178980269,2	MCF-7	breast:
6	chr3:178790486..178793046-chr3:179039770..179041541,2	K562	blood:
7	chr3:178787966..178791118-chr3:178865051..178866959,3	MCF-7	breast:
8	chr3:178786925..178790579-chr3:178864297..178867679,5	K562	blood:
9	chr3:178787982..178790546-chr3:179037129..179041546,5	MCF-7	breast:
10	chr3:178787639..178789990-chr3:179064273..179066880,2	MCF-7	breast:
11	chr3:178788594..178790647-chr3:179063924..179066564,2	K562	blood:
12	chr3:178786609..178788978-chr3:178792801..178794619,2	MCF-7	breast:
13	chr3:178787618..178789818-chr3:179039518..179042108,2	K562	blood:
14	chr3:178787120..178791261-chr3:179039253..179041998,3	K562	blood:

No data

Variant related genes	Relation type
ZMAT3	TF binding region
ZMAT3	CpG island
ENSG00000200616	chromatin interactions
ENSG00000171109	chromatin interactions
ENSG00000240429	chromatin interactions
ENSG00000121864	chromatin interactions
ENSG00000121879	chromatin interactions
ENSG00000229102	chromatin interactions

Extended variants
information (count: 83 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:83 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369827160	chr3:178788513-178788514	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs546834187	chr3:178788575-178788576	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs140640038	chr3:178788605-178788606	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs118116940	chr3:178788623-178788624	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs551749546	chr3:178788645-178788646	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs568549360	chr3:178788688-178788689	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs530998169	chr3:178788693-178788694	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs372400529	chr3:178788713-178788714	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs377519831	chr3:178788720-178788721	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs551517785	chr3:178788766-178788767	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs544017030	chr3:178788856-178788857	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs201231832	chr3:178788868-178788869	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs183416359	chr3:178788871-178788872	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs115292441	chr3:178788874-178788875	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs573453156	chr3:178788877-178788878	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs545724453	chr3:178788904-178788905	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs558976165	chr3:178789025-178789026	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs575736418	chr3:178789080-178789081	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs544687852	chr3:178789151-178789152	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs375450894	chr3:178789196-178789197	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs561378923	chr3:178789213-178789214	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs529851701	chr3:178789255-178789256	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs142158479	chr3:178789258-178789259	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs560336313	chr3:178789287-178789288	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs186133356	chr3:178789292-178789293	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs552083902	chr3:178789294-178789295	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs546976835	chr3:178789319-178789320	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs531223917	chr3:178789324-178789325	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs547838635	chr3:178789354-178789355	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs150762965	chr3:178789507-178789508	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs370954576	chr3:178789526-178789527	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs533931712	chr3:178789534-178789535	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs546869472	chr3:178789564-178789565	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs190576591	chr3:178789576-178789577	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs567088157	chr3:178789623-178789624	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs112855977	chr3:178789652-178789653	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs375451268	chr3:178789707-178789708	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs559312613	chr3:178789712-178789713	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs6774158	chr3:178789724-178789725	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs538246622	chr3:178789726-178789727	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs76371047	chr3:178789815-178789816	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs574828730	chr3:178789821-178789822	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs111356558	chr3:178789897-178789898	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs534885738	chr3:178789898-178789899	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs183463682	chr3:178789918-178789919	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs139159699	chr3:178789991-178789992	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs557998389	chr3:178790026-178790027	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs368900448	chr3:178790103-178790104	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs545660142	chr3:178790140-178790141	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs61798205	chr3:178790161-178790162	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Anaplastic thyroid cancer	17989125	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Ovarian cancer	18208621	CNVD
Thyroid cancer	17317825	CNVD
Thyroid cancer	17989125	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	21806811	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	19653912	CNVD
Endometrial cancer	19261849	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:399 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:178756800-178788800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr3:178764800-178789000	Weak transcription	Lung	lung
3	chr3:178765200-178789000	Weak transcription	Spleen	Spleen
4	chr3:178768400-178788800	Weak transcription	Small Intestine	intestine
5	chr3:178768600-178788800	Weak transcription	Placenta	Placenta
6	chr3:178772600-178788800	Weak transcription	Esophagus	oesophagus
7	chr3:178773600-178788600	Weak transcription	Fetal Stomach	stomach
8	chr3:178778200-178788600	Weak transcription	Primary hematopoietic stem cells	blood
9	chr3:178780200-178788800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr3:178782600-178788800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr3:178782600-178788800	Weak transcription	Psoas Muscle	Psoas
12	chr3:178783400-178788600	Weak transcription	Right Ventricle	heart
13	chr3:178784800-178788800	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr3:178785400-178788600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr3:178785400-178788600	Weak transcription	Fetal Muscle Leg	muscle
16	chr3:178785600-178788600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr3:178785600-178788800	Weak transcription	Fetal Muscle Trunk	muscle
18	chr3:178785600-178788800	Weak transcription	Ovary	ovary
19	chr3:178785600-178790000	Active TSS	GM12878-XiMat	blood
20	chr3:178785800-178788600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr3:178786000-178789000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr3:178786000-178789000	Weak transcription	Gastric	stomach
23	chr3:178786200-178789000	Weak transcription	Pancreas	Pancrea
24	chr3:178786600-178789200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr3:178786600-178790200	Active TSS	Brain Inferior Temporal Lobe	brain
26	chr3:178786800-178788600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
27	chr3:178786800-178788600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr3:178786800-178788800	Weak transcription	Left Ventricle	heart
29	chr3:178786800-178789800	Active TSS	NH-A	brain
30	chr3:178787000-178788600	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr3:178787000-178788600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
32	chr3:178787000-178789600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr3:178787000-178789800	Active TSS	HUES6 Cell Line	embryonic stem cell
34	chr3:178787000-178789800	Active TSS	Cortex derived primary cultured neurospheres	brain
35	chr3:178787000-178790000	Active TSS	NHDF-Ad	bronchial
36	chr3:178787000-178790200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr3:178787000-178790200	Active TSS	HSMMtube	muscle
38	chr3:178787000-178790400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr3:178787200-178788800	Flanking Active TSS	NHEK	skin
40	chr3:178787200-178789800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr3:178787200-178790200	Active TSS	Breast Myoepithelial Primary Cells	Breast
42	chr3:178787200-178790200	Active TSS	NHLF	lung
43	chr3:178787200-178790400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr3:178787400-178788600	Active TSS	HepG2	liver
45	chr3:178787400-178789800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr3:178787400-178789800	Active TSS	HMEC	breast
47	chr3:178787400-178790000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr3:178787400-178790200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr3:178787400-178790200	Active TSS	Thymus	Thymus
50	chr3:178787400-178790400	Active TSS	A549	lung

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