Variant report

Variant	esv3343605
Chromosome Location	chr2:46925273-46927821
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:803)
CpG islands
(count:733)
Chromatin interactive
region (count:13)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:803 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:46925574-46925960	K562	blood:	n/a	n/a
2	ARID3A	chr2:46924704-46926145	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:46926821-46926840	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:46927741-46927927	K562	blood:	n/a	n/a
5	ATF2	chr2:46925530-46926151	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr2:46925586-46926235	GM12878	blood:	n/a	n/a
7	ATF2	chr2:46925588-46926084	GM12878	blood:	n/a	n/a
8	ATF3	chr2:46925752-46926184	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr2:46925762-46926139	HepG2	liver:	n/a	n/a
10	ATF3	chr2:46925510-46926228	HepG2	liver:	n/a	chr2:46925661-46925670
11	ATF3	chr2:46925735-46926125	GM12878	blood:	n/a	n/a
12	ATF3	chr2:46925402-46926246	A549	lung:	n/a	chr2:46925661-46925670
13	ATF3	chr2:46925672-46926127	GM12878	blood:	n/a	n/a
14	ATF3	chr2:46925628-46926257	H1-hESC	embryonic stem cell:	n/a	chr2:46925661-46925670
15	ATF3	chr2:46925728-46926186	K562	blood:	n/a	n/a
16	BACH1	chr2:46926838-46926987	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr2:46925618-46926112	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL3	chr2:46925291-46926156	A549	lung:	n/a	chr2:46925639-46925648 chr2:46925506-46925519 chr2:46925838-46925847
19	BCL3	chr2:46925504-46926171	A549	lung:	n/a	chr2:46925639-46925648 chr2:46925506-46925519 chr2:46925838-46925847
20	BHLHE40	chr2:46925461-46926263	HepG2	liver:	n/a	n/a
21	BHLHE40	chr2:46925572-46926280	K562	blood:	n/a	n/a
22	BHLHE40	chr2:46926499-46926956	HepG2	liver:	n/a	n/a
23	BHLHE40	chr2:46926823-46926932	K562	blood:	n/a	n/a
24	BHLHE40	chr2:46925540-46926328	GM12878	blood:	n/a	n/a
25	BRCA1	chr2:46926847-46926889	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr2:46925405-46926193	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr2:46926633-46926802	HepG2	liver:	n/a	n/a
28	BRCA1	chr2:46925703-46925892	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr2:46925603-46925913	HepG2	liver:	n/a	n/a
30	CBX3	chr2:46925657-46925933	K562	blood:	n/a	n/a
31	CBX3	chr2:46925392-46926259	K562	blood:	n/a	n/a
32	CCNT2	chr2:46925786-46926881	K562	blood:	n/a	n/a
33	CEBPB	chr2:46927620-46927917	IMR90	lung:	n/a	chr2:46927769-46927780
34	CEBPB	chr2:46927615-46927932	HepG2	liver:	n/a	chr2:46927769-46927780
35	CEBPB	chr2:46927626-46927913	A549	lung:	n/a	chr2:46927769-46927780
36	CEBPB	chr2:46925458-46925481	K562	blood:	n/a	n/a
37	CEBPB	chr2:46927465-46928062	A549	lung:	n/a	chr2:46927769-46927780
38	CEBPB	chr2:46927596-46927927	K562	blood:	n/a	chr2:46927769-46927780
39	CEBPB	chr2:46927615-46927921	Hela-S3	cervix:	n/a	chr2:46927769-46927780
40	CEBPB	chr2:46925562-46926159	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr2:46927648-46927863	H1-hESC	embryonic stem cell:	n/a	chr2:46927769-46927780
42	CEBPD	chr2:46925544-46926963	HepG2	liver:	n/a	n/a
43	CEBPD	chr2:46925712-46926540	HepG2	liver:	n/a	n/a
44	CHD1	chr2:46925099-46929421	IMR90	lung:	n/a	n/a
45	CHD1	chr2:46926672-46926899	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr2:46925518-46926132	GM12878	blood:	n/a	n/a
47	CHD1	chr2:46925513-46925993	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD1	chr2:46926470-46926510	GM12878	blood:	n/a	n/a
49	CHD2	chr2:46925601-46926376	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr2:46925668-46926583	HepG2	liver:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:46926217-46926267	A549	lung:	n/a
2	chr2:46926217-46926267	A549	lung:	n/a
3	chr2:46927010-46927060	HL-60	blood:	n/a
4	chr2:46926069-46926119	MCF10A-Er-Src	breast:	n/a
5	chr2:46926272-46926322	NT2-D1	testis:	n/a
6	chr2:46926272-46926322	A549	lung:	n/a
7	chr2:46925381-46925431	ProgFib	skin:	n/a
8	chr2:46927010-46927060	GM19239	blood:	n/a
9	chr2:46926944-46926994	NB4	blood:	n/a
10	chr2:46926217-46926267	CMK	blood:	n/a
11	chr2:46926433-46926483	GM19239	blood:	n/a
12	chr2:46925753-46925803	MCF-7	breast:	n/a
13	chr2:46926842-46926892	AG04450	lung:	fetal
14	chr2:46926433-46926483	T-47D	breast:	n/a
15	chr2:46925381-46925431	Hela-S3	cervix:	n/a
16	chr2:46925333-46925383	PrEC	prostate:	n/a
17	chr2:46925970-46926020	AoSMC	blood vessel:	n/a
18	chr2:46926842-46926892	SAEC	small airway:	n/a
19	chr2:46926944-46926994	Hepatocyte	liver:	n/a
20	chr2:46925381-46925431	AG04450	lung:	fetal
21	chr2:46925970-46926020	HEEpiC	esophagus:	n/a
22	chr2:46926190-46926240	SKMC	muscle:	n/a
23	chr2:46926433-46926483	H1-hESC	embryonic stem cell:	embryo
24	chr2:46925970-46926020	HCM	heart:	n/a
25	chr2:46926842-46926892	AG04449	skin:	fetal
26	chr2:46926842-46926892	CMK	blood:	n/a
27	chr2:46925333-46925383	ProgFib	skin:	n/a
28	chr2:46925970-46926020	PANC-1	pancreas:	n/a
29	chr2:46925333-46925383	Hepatocyte	liver:	n/a
30	chr2:46925970-46926020	AG04449	skin:	fetal
31	chr2:46926069-46926119	NHBE	bronchial:	n/a
32	chr2:46925753-46925803	GM12878	blood:	n/a
33	chr2:46926217-46926267	SAEC	small airway:	n/a
34	chr2:46925753-46925803	H1-hESC	embryonic stem cell:	embryo
35	chr2:46925333-46925383	MCF-7	breast:	n/a
36	chr2:46926944-46926994	T-47D	breast:	n/a
37	chr2:46926217-46926267	HPAEpiC	pulmonary alveolar:	n/a
38	chr2:46925381-46925431	ECC-1	luminal epithelium:	n/a
39	chr2:46925970-46926020	HUVEC	blood vessel:	n/a
40	chr2:46926217-46926267	MCF-7	breast:	n/a
41	chr2:46925753-46925803	HCM	heart:	n/a
42	chr2:46926944-46926994	HepG2	liver:	n/a
43	chr2:46926944-46926994	HRCEpiC	kidney:	n/a
44	chr2:46925970-46926020	HPAEpiC	pulmonary alveolar:	n/a
45	chr2:46925753-46925803	SK-N-SH_RA	brain:	n/a
46	chr2:46926433-46926483	HNPCEpiC	eye:	n/a
47	chr2:46927010-46927060	NT2-D1	testis:	n/a
48	chr2:46926190-46926240	AG10803	skin:	n/a
49	chr2:46926272-46926322	NHBE	bronchial:	n/a
50	chr2:46927010-46927060	HepG2	liver:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:46842180..46843861-chr2:46924432..46926384,2	K562	blood:
2	chr2:46926271..46927170-chr7:26240072..26240761,2	Hela-S3	cervix:
3	chr2:46923714..46925684-chr2:46963885..46966277,2	MCF-7	breast:
4	chr2:46919753..46923455-chr2:46923473..46925760,5	K562	blood:
5	chr2:46916264..46918533-chr2:46923065..46926019,3	K562	blood:
6	chr2:46923183..46926073-chr2:46944483..46946206,2	K562	blood:
7	chr2:46926377..46928977-chr2:47022030..47023631,2	K562	blood:
8	chr15:41047268..41048047-chr2:46926297..46927002,2	Hela-S3	cervix:
9	chr2:46915855..46917491-chr2:46923839..46925378,2	MCF-7	breast:
10	chr2:46926502..46928230-chr2:46967700..46969222,2	MCF-7	breast:
11	chr2:46897133..46898995-chr2:46922668..46925477,2	K562	blood:
12	chr2:46925509..46928130-chr2:47135510..47137063,2	MCF-7	breast:
13	chr2:46926353..46928054-chr2:46945073..46946618,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PIGF-4	chr2:46926027-46926053	NONHSAT070524
2	lnc-CRIPT-4	chr2:46926519-46927680	ucscGeneNc_uc002rvj_1
3	lnc-PIGF-4	chr2:46925253-46925831	NONHSAT070524

No data

Variant related genes	Relation type
SOCS5	TF binding region
SOCS5	CpG island
ENSG00000180398	chromatin interactions
ENSG00000119878	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000137824	chromatin interactions

Extended variants
information (count: 105 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:105 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372497056	chr2:46925356-46925357	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
2	rs41452946	chr2:46925379-46925380	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs540990161	chr2:46925388-46925389	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs182281805	chr2:46925392-46925393	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs377391051	chr2:46925396-46925397	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs35680299	chr2:46925430-46925431	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs562965556	chr2:46925439-46925440	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs371395117	chr2:46925461-46925462	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs35436479	chr2:46925485-46925486	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs527704859	chr2:46925505-46925506	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs35750425	chr2:46925512-46925513	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs112033770	chr2:46925528-46925529	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
13	rs561348080	chr2:46925533-46925534	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
14	rs531760011	chr2:46925559-46925560	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
15	rs13386416	chr2:46925572-46925573	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
16	rs186821072	chr2:46925579-46925580	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
17	rs571750603	chr2:46925599-46925600	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
18	rs190344190	chr2:46925625-46925626	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
19	rs547700089	chr2:46925647-46925648	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
20	rs376147440	chr2:46925670-46925671	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
21	rs41501846	chr2:46925672-46925673	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs377687346	chr2:46925687-46925688	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
23	rs4952842	chr2:46925730-46925731	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs185459620	chr2:46925747-46925748	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
25	rs41389052	chr2:46925781-46925782	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs3829835	chr2:46925789-46925790	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs189872419	chr2:46925810-46925811	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
28	rs531929151	chr2:46925846-46925847	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs140070047	chr2:46925854-46925855	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs3814040	chr2:46925859-46925860	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs41504048	chr2:46925860-46925861	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs77033967	chr2:46925865-46925866	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs554095220	chr2:46925889-46925890	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs368171045	chr2:46925910-46925911	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs572398613	chr2:46925958-46925959	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs543041470	chr2:46925993-46925994	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs550135057	chr2:46926010-46926011	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs561307575	chr2:46926022-46926023	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs531791864	chr2:46926027-46926028	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
40	rs41417248	chr2:46926034-46926035	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
41	rs3814039	chr2:46926064-46926065	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs565441775	chr2:46926103-46926104	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs532581129	chr2:46926111-46926112	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs547612020	chr2:46926120-46926121	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs566027073	chr2:46926133-46926134	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs530363404	chr2:46926144-46926145	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs13000826	chr2:46926146-46926147	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs373827923	chr2:46926155-46926156	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs367676726	chr2:46926200-46926201	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs111677684	chr2:46926422-46926423	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Myelofibrosis	22110671	CNVD
Hypotonia	17579669	CNVD
Hypotonia-Cystinuria syndrome	16385448	CNVD
Glioblastoma multiforme	17002787	CNVD
Cystinuria	17625506	CNVD
Breast cancer	16272173	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Ovarian cancer	22355333	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:391 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:46922600-46925400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr2:46924600-46929200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr2:46924800-46925400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
4	chr2:46924800-46925400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr2:46924800-46925400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr2:46924800-46925400	Enhancers	Placenta	Placenta
7	chr2:46924800-46925600	Enhancers	Gastric	stomach
8	chr2:46924800-46925600	Enhancers	Lung	lung
9	chr2:46924800-46925600	Enhancers	Sigmoid Colon	Sigmoid Colon
10	chr2:46924800-46925800	Flanking Active TSS	Dnd41	blood
11	chr2:46924800-46928200	Active TSS	Duodenum Smooth Muscle	Duodenum
12	chr2:46925000-46925400	Enhancers	H1 Cell Line	embryonic stem cell
13	chr2:46925000-46925400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
14	chr2:46925000-46925400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
15	chr2:46925000-46925400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr2:46925000-46925400	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr2:46925000-46925400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
18	chr2:46925000-46925400	Enhancers	Fetal Kidney	kidney
19	chr2:46925000-46925400	Flanking Active TSS	Rectal Smooth Muscle	rectum
20	chr2:46925000-46925400	Enhancers	NHLF	lung
21	chr2:46925000-46925600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr2:46925000-46925600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
23	chr2:46925000-46925600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
24	chr2:46925000-46925600	Flanking Active TSS	Brain Hippocampus Middle	brain
25	chr2:46925000-46925600	Flanking Active TSS	Colonic Mucosa	Colon
26	chr2:46925000-46925600	Enhancers	Fetal Brain Male	brain
27	chr2:46925000-46925600	Enhancers	Stomach Mucosa	stomach
28	chr2:46925000-46925600	Flanking Active TSS	A549	lung
29	chr2:46925000-46925600	Flanking Active TSS	Hela-S3	cervix
30	chr2:46925000-46925600	Enhancers	NHDF-Ad	bronchial
31	chr2:46925000-46925800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr2:46925000-46925800	Weak transcription	Small Intestine	intestine
33	chr2:46925000-46926000	Flanking Active TSS	K562	blood
34	chr2:46925000-46927200	Active TSS	Brain Inferior Temporal Lobe	brain
35	chr2:46925000-46927200	Active TSS	Duodenum Mucosa	Duodenum
36	chr2:46925000-46928400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr2:46925000-46930000	Active TSS	Breast Myoepithelial Primary Cells	Breast
38	chr2:46925200-46925400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
39	chr2:46925200-46925400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr2:46925200-46925400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
41	chr2:46925200-46925400	Flanking Active TSS	Primary T cells from cord blood	blood
42	chr2:46925200-46925400	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr2:46925200-46925400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
44	chr2:46925200-46925400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr2:46925200-46925400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
46	chr2:46925200-46925400	Flanking Active TSS	Brain Angular Gyrus	brain
47	chr2:46925200-46925400	Flanking Active TSS	Colon Smooth Muscle	Colon
48	chr2:46925200-46925400	Flanking Active TSS	Fetal Intestine Large	intestine
49	chr2:46925200-46925400	Enhancers	Fetal Lung	lung
50	chr2:46925200-46925400	Enhancers	Fetal Muscle Leg	muscle

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