Variant report

Variant	esv18196
Chromosome Location	chr3:75721698-75794795
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2087)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:3)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:2087 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:75739156-75739286	K562	blood:	n/a	n/a
2	ARID3A	chr3:75754843-75755270	K562	blood:	n/a	n/a
3	ARID3A	chr3:75736701-75737480	K562	blood:	n/a	n/a
4	ARID3A	chr3:75770122-75770154	HepG2	liver:	n/a	n/a
5	ATF1	chr3:75755512-75756182	K562	blood:	n/a	n/a
6	ATF1	chr3:75771441-75772260	K562	blood:	n/a	n/a
7	ATF1	chr3:75783726-75784839	K562	blood:	n/a	n/a
8	ATF1	chr3:75789795-75794952	K562	blood:	n/a	n/a
9	ATF1	chr3:75765400-75768808	K562	blood:	n/a	n/a
10	ATF1	chr3:75773435-75776229	K562	blood:	n/a	n/a
11	ATF1	chr3:75726782-75726783	K562	blood:	n/a	n/a
12	ATF1	chr3:75743644-75744222	K562	blood:	n/a	n/a
13	ATF1	chr3:75785062-75787392	K562	blood:	n/a	n/a
14	ATF1	chr3:75750030-75750205	K562	blood:	n/a	n/a
15	ATF1	chr3:75763746-75764601	K562	blood:	n/a	n/a
16	ATF1	chr3:75728107-75728162	K562	blood:	n/a	n/a
17	ATF1	chr3:75734703-75734852	K562	blood:	n/a	n/a
18	ATF1	chr3:75769325-75769986	K562	blood:	n/a	n/a
19	ATF1	chr3:75736867-75738707	K562	blood:	n/a	n/a
20	ATF1	chr3:75760657-75761408	K562	blood:	n/a	n/a
21	ATF1	chr3:75777037-75777776	K562	blood:	n/a	n/a
22	ATF1	chr3:75745544-75745744	K562	blood:	n/a	n/a
23	ATF1	chr3:75747229-75747380	K562	blood:	n/a	n/a
24	ATF1	chr3:75740338-75740804	K562	blood:	n/a	n/a
25	ATF1	chr3:75787686-75789584	K562	blood:	n/a	n/a
26	ATF1	chr3:75730688-75730845	K562	blood:	n/a	n/a
27	ATF1	chr3:75754856-75755222	K562	blood:	n/a	n/a
28	ATF1	chr3:75761625-75762259	K562	blood:	n/a	n/a
29	ATF1	chr3:75728521-75728535	K562	blood:	n/a	n/a
30	ATF1	chr3:75735197-75735394	K562	blood:	n/a	n/a
31	ATF1	chr3:75779002-75782622	K562	blood:	n/a	n/a
32	ATF1	chr3:75735948-75736287	K562	blood:	n/a	n/a
33	ATF1	chr3:75746545-75746765	K562	blood:	n/a	n/a
34	ATF1	chr3:75778219-75778585	K562	blood:	n/a	n/a
35	ATF1	chr3:75762715-75762961	K562	blood:	n/a	n/a
36	ATF1	chr3:75733400-75734148	K562	blood:	n/a	n/a
37	ATF1	chr3:75759504-75760427	K562	blood:	n/a	n/a
38	ATF3	chr3:75788958-75789896	K562	blood:	n/a	n/a
39	BACH1	chr3:75736972-75737792	K562	blood:	n/a	n/a
40	BACH1	chr3:75720730-75721914	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr3:75734445-75734852	K562	blood:	n/a	n/a
42	BACH1	chr3:75744812-75745060	K562	blood:	n/a	n/a
43	BACH1	chr3:75740483-75740494	K562	blood:	n/a	n/a
44	BACH1	chr3:75739253-75739499	K562	blood:	n/a	n/a
45	BACH1	chr3:75787478-75787482	K562	blood:	n/a	n/a
46	BACH1	chr3:75735200-75735345	K562	blood:	n/a	n/a
47	BATF	chr3:75733538-75733934	GM12878	blood:	n/a	chr3:75733714-75733723
48	BCL11A	chr3:75723396-75723619	GM12878	blood:	n/a	n/a
49	BCL11A	chr3:75730792-75731137	GM12878	blood:	n/a	n/a
50	BCL3	chr3:75768536-75768746	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75721888-75721938	SK-N-MC	brain:	n/a
2	chr3:75721888-75721938	Caco-2	colon:	n/a
3	chr3:75721888-75721938	AG09309	skin:	n/a
4	chr3:75721888-75721938	BJ	skin:	n/a
5	chr3:75721888-75721938	AG04450	lung:	fetal
6	chr3:75721888-75721938	A549	lung:	n/a
7	chr3:75721888-75721938	HEEpiC	esophagus:	n/a
8	chr3:75721888-75721938	ovcar-3	ovarian:	n/a
9	chr3:75721888-75721938	IMR90	lung:	fetal
10	chr3:75721888-75721938	MCF-7	breast:	n/a
11	chr3:75721888-75721938	NHDF-neo	bronchial:	n/a
12	chr3:75721888-75721938	HepG2	liver:	n/a
13	chr3:75721888-75721938	HPAEpiC	pulmonary alveolar:	n/a
14	chr3:75721888-75721938	HRCEpiC	kidney:	n/a
15	chr3:75721888-75721938	Hepatocyte	liver:	n/a
16	chr3:75721888-75721938	HAEpiC	amniotic membrane:	n/a
17	chr3:75721888-75721938	NT2-D1	testis:	n/a
18	chr3:75721888-75721938	GM12892	blood:	n/a
19	chr3:75721888-75721938	NH-A	brain:	n/a
20	chr3:75721888-75721938	HNPCEpiC	eye:	n/a
21	chr3:75721888-75721938	HRPEpiC	eye:	n/a
22	chr3:75721888-75721938	HCPEpiC	choroid plexus:	n/a
23	chr3:75721888-75721938	Jurkat	blood:	n/a
24	chr3:75721888-75721938	K562	blood:	n/a
25	chr3:75721888-75721938	SK-N-SH_RA	brain:	n/a
26	chr3:75721888-75721938	GM19239	blood:	n/a
27	chr3:75721888-75721938	Hela-S3	cervix:	n/a
28	chr3:75721888-75721938	HIPEpiC	eye:	n/a
29	chr3:75721888-75721938	LNCaP	prostate:	n/a
30	chr3:75721888-75721938	AoSMC	blood vessel:	n/a
31	chr3:75721888-75721938	HL-60	blood:	n/a
32	chr3:75721888-75721938	HUVEC	blood vessel:	n/a
33	chr3:75721888-75721938	MCF10A-Er-Src	breast:	n/a
34	chr3:75721888-75721938	GM12878	blood:	n/a
35	chr3:75721888-75721938	GM12891	blood:	n/a
36	chr3:75721888-75721938	CMK	blood:	n/a
37	chr3:75721888-75721938	U87	brain:	n/a
38	chr3:75721888-75721938	T-47D	breast:	n/a
39	chr3:75721888-75721938	AG09319	gingival:	n/a
40	chr3:75721888-75721938	AG10803	skin:	n/a
41	chr3:75721888-75721938	HEK293	kidney:	embryo
42	chr3:75721888-75721938	ProgFib	skin:	n/a
43	chr3:75721888-75721938	SKMC	muscle:	n/a
44	chr3:75721888-75721938	H1-hESC	embryonic stem cell:	embryo
45	chr3:75721888-75721938	NB4	blood:	n/a
46	chr3:75721888-75721938	HMEC	breast:	n/a
47	chr3:75721888-75721938	HRE	kidney:	n/a
48	chr3:75721888-75721938	AG04449	skin:	fetal
49	chr3:75721888-75721938	HCM	heart:	n/a
50	chr3:75721888-75721938	NHBE	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:56709052..56711813-chr3:75770362..75772517,2	MCF-7	breast:
2	chr3:75790783..75791412-chr6:15280318..15280818,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNTN3-1	chr3:75762167-75762465	NONHSAT090550
2	lnc-FRG2C-1	chr3:75723564-75725031	ENSG00000242516
3	lnc-FRG2C-1	chr3:75725119-75725776	ENSG00000242516

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4273	chr3:75787441-75787458	MIMAT0016903

No data

Variant related genes	Relation type
MIR4273	TF binding region
LINC00960	TF binding region
RN7SL92P	TF binding region
MIR4273	CpG island
LINC00960	CpG island
RN7SL92P	CpG island
ENSG00000212195	chromatin interactions

Extended variants
information (count: 7890 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:7890 , 50 per page) page: 1 2 3 4 5 6 7 ... 158

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73126905	chr3:75721706-75721707	Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs73126906	chr3:75721711-75721712	Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs142313364	chr3:75721727-75721728	Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs190409183	chr3:75721735-75721736	Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs79829469	chr3:75721766-75721767	Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs75797840	chr3:75721771-75721772	Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs200936499	chr3:75721772-75721773	Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs114040091	chr3:75721800-75721801	Bivalent/Poised TSS Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs199887717	chr3:75721810-75721811	Active TSS Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs201011443	chr3:75721812-75721813	Active TSS Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs77049246	chr3:75721818-75721819	Active TSS Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs376427884	chr3:75721836-75721837	Active TSS Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs78478664	chr3:75721841-75721842	Active TSS Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs116836387	chr3:75721869-75721870	Active TSS Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs73126910	chr3:75721881-75721882	Active TSS Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs73126911	chr3:75721919-75721920	Active TSS Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs73126913	chr3:75721923-75721924	Active TSS Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs78764696	chr3:75721934-75721935	Active TSS Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs61028084	chr3:75721946-75721947	Active TSS Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs7340650	chr3:75721948-75721949	Active TSS Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs74968750	chr3:75722002-75722003	Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs78939212	chr3:75722029-75722030	Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs201367633	chr3:75722031-75722032	Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs370117502	chr3:75722064-75722065	Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs373287544	chr3:75722073-75722074	Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs200970316	chr3:75722077-75722078	Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs7340654	chr3:75722081-75722082	Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs78417794	chr3:75722088-75722089	Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs143079051	chr3:75722120-75722121	Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs199667886	chr3:75722125-75722126	Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs139199025	chr3:75722140-75722141	Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs79194723	chr3:75722145-75722146	Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs369559982	chr3:75722146-75722147	Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs372935695	chr3:75722149-75722150	Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs202243341	chr3:75722152-75722153	Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs78948098	chr3:75722153-75722154	Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs200553912	chr3:75722156-75722157	Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs75347692	chr3:75722158-75722159	Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs149892974	chr3:75722159-75722160	Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs146178032	chr3:75722172-75722173	Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs78281302	chr3:75722185-75722186	Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs113630227	chr3:75722188-75722189	Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs76976444	chr3:75722227-75722228	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs375942983	chr3:75722239-75722240	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs370877716	chr3:75722242-75722243	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs201588389	chr3:75722244-75722245	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs73840362	chr3:75722258-75722259	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs8179957	chr3:75722260-75722261	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs201091935	chr3:75722274-75722275	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs183670964	chr3:75722287-75722288	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	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
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Autism	22102821	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Ovarian cancer	21720365	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:804 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75716600-75722400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr3:75716800-75721800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:75716800-75721800	ZNF genes & repeats	Rectal Smooth Muscle	rectum
4	chr3:75716800-75722000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr3:75716800-75722000	ZNF genes & repeats	Pancreas	Pancrea
6	chr3:75716800-75722400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
7	chr3:75717000-75721800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
8	chr3:75717000-75721800	ZNF genes & repeats	Brain Substantia Nigra	brain
9	chr3:75717000-75721800	ZNF genes & repeats	Gastric	stomach
10	chr3:75717000-75721800	ZNF genes & repeats	Spleen	Spleen
11	chr3:75717000-75722000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr3:75717000-75722600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr3:75717200-75722000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
14	chr3:75717200-75722400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
15	chr3:75717400-75722600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
16	chr3:75717600-75721800	ZNF genes & repeats	Colonic Mucosa	Colon
17	chr3:75718000-75721800	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
18	chr3:75718000-75721800	ZNF genes & repeats	Dnd41	blood
19	chr3:75718200-75722000	ZNF genes & repeats	Right Atrium	heart
20	chr3:75718600-75722000	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
21	chr3:75718600-75722400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr3:75718800-75721800	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
23	chr3:75719000-75721800	ZNF genes & repeats	HMEC	breast
24	chr3:75719000-75722000	ZNF genes & repeats	Lung	lung
25	chr3:75719000-75722600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
26	chr3:75719200-75722400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr3:75719200-75722600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
28	chr3:75719400-75722000	Bivalent/Poised TSS	NHLF	lung
29	chr3:75719600-75722400	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr3:75719800-75722600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
31	chr3:75720000-75721800	Bivalent/Poised TSS	NHEK	skin
32	chr3:75720000-75722400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr3:75720000-75722600	Active TSS	NHDF-Ad	bronchial
34	chr3:75720200-75722400	ZNF genes & repeats	Placenta Amnion	Placenta Amnion
35	chr3:75720400-75721800	Bivalent/Poised TSS	Adipose Nuclei	Adipose
36	chr3:75720400-75722000	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr3:75720400-75722200	Bivalent/Poised TSS	Fetal Kidney	kidney
38	chr3:75720400-75722600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr3:75720400-75722600	Active TSS	NH-A	brain
40	chr3:75720600-75721800	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
41	chr3:75720600-75722400	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr3:75720800-75721800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
43	chr3:75720800-75722000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
44	chr3:75720800-75722000	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
45	chr3:75720800-75722000	ZNF genes & repeats	Aorta	Aorta
46	chr3:75720800-75722000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
47	chr3:75720800-75722000	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
48	chr3:75720800-75722400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
49	chr3:75720800-75722600	Active TSS	Muscle Satellite Cultured Cells	--
50	chr3:75721000-75722000	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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