Variant report

Variant	esv3380825
Chromosome Location	chr2:211035207-211037105
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:690)
CpG islands
(count:793)
Chromatin interactive
region (count:17)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:690 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:211034666-211035725	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:211036085-211036810	HepG2	liver:	n/a	n/a
3	ATF2	chr2:211035053-211035556	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr2:211035115-211035473	GM12878	blood:	n/a	n/a
5	ATF2	chr2:211034988-211035553	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr2:211035184-211035750	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr2:211035279-211035557	K562	blood:	n/a	n/a
8	ATF3	chr2:211035196-211035765	HepG2	liver:	n/a	n/a
9	ATF3	chr2:211035367-211035687	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr2:211035083-211035750	GM12878	blood:	n/a	n/a
11	ATF3	chr2:211035403-211035680	GM12878	blood:	n/a	n/a
12	ATF3	chr2:211035364-211035689	K562	blood:	n/a	n/a
13	ATF3	chr2:211035318-211035725	HepG2	liver:	n/a	n/a
14	BACH1	chr2:211036201-211036654	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL3	chr2:211036014-211036594	A549	lung:	n/a	chr2:211036210-211036219 chr2:211036211-211036220
16	BCL3	chr2:211035969-211036393	GM12878	blood:	n/a	chr2:211036210-211036219 chr2:211036211-211036220
17	BCLAF1	chr2:211034662-211035408	GM12878	blood:	n/a	n/a
18	BHLHE40	chr2:211035053-211036619	HepG2	liver:	n/a	chr2:211035570-211035583 chr2:211036081-211036097 chr2:211036220-211036236
19	BHLHE40	chr2:211034818-211036612	K562	blood:	n/a	chr2:211035570-211035583 chr2:211036081-211036097 chr2:211036220-211036236
20	BHLHE40	chr2:211035321-211035753	HepG2	liver:	n/a	chr2:211035570-211035583
21	BHLHE40	chr2:211034644-211036595	GM12878	blood:	n/a	chr2:211035570-211035583 chr2:211036081-211036097 chr2:211036220-211036236
22	BRCA1	chr2:211034403-211035579	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr2:211035779-211035921	HepG2	liver:	n/a	n/a
24	BRCA1	chr2:211035769-211035793	GM12878	blood:	n/a	n/a
25	BRCA1	chr2:211034950-211035533	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr2:211036180-211036466	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr2:211036248-211036475	HepG2	liver:	n/a	n/a
28	CBX3	chr2:211036079-211036406	K562	blood:	n/a	n/a
29	CCNT2	chr2:211035093-211036611	K562	blood:	n/a	chr2:211036173-211036182 chr2:211035598-211035607 chr2:211036225-211036234 chr2:211035564-211035573
30	CEBPB	chr2:211034654-211035858	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:211034521-211035683	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr2:211036096-211036485	MCF-7	breast:	n/a	n/a
33	CEBPB	chr2:211034981-211035682	MCF-7	breast:	n/a	n/a
34	CEBPB	chr2:211035080-211035649	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr2:211034990-211035693	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr2:211035368-211035570	K562	blood:	n/a	n/a
37	CEBPB	chr2:211035233-211035699	HepG2	liver:	n/a	n/a
38	CEBPB	chr2:211035047-211035736	A549	lung:	n/a	n/a
39	CEBPB	chr2:211034613-211035675	K562	blood:	n/a	n/a
40	CEBPB	chr2:211034618-211035679	A549	lung:	n/a	n/a
41	CEBPB	chr2:211035350-211035609	HepG2	liver:	n/a	n/a
42	CEBPB	chr2:211034546-211035876	IMR90	lung:	n/a	n/a
43	CEBPB	chr2:211035229-211035581	K562	blood:	n/a	n/a
44	CEBPB	chr2:211035119-211036372	HepG2	liver:	n/a	n/a
45	CEBPB	chr2:211035035-211035738	MCF-7	breast:	n/a	n/a
46	CEBPB	chr2:211035271-211035567	A549	lung:	n/a	n/a
47	CEBPD	chr2:211035294-211035715	K562	blood:	n/a	n/a
48	CEBPD	chr2:211035084-211036357	HepG2	liver:	n/a	n/a
49	CEBPD	chr2:211035338-211035765	HepG2	liver:	n/a	n/a
50	CHD1	chr2:211037089-211037394	H1-hESC	embryonic stem cell:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:211036599-211036649	HIPEpiC	eye:	n/a
2	chr2:211035202-211035252	HNPCEpiC	eye:	n/a
3	chr2:211035360-211035410	SK-N-SH_RA	brain:	n/a
4	chr2:211035960-211036010	GM12891	blood:	n/a
5	chr2:211035530-211035580	Jurkat	blood:	n/a
6	chr2:211036478-211036528	MCF10A-Er-Src	breast:	n/a
7	chr2:211035422-211035472	GM19239	blood:	n/a
8	chr2:211036599-211036649	HUVEC	blood vessel:	n/a
9	chr2:211035530-211035580	Hela-S3	cervix:	n/a
10	chr2:211035526-211035576	HepG2	liver:	n/a
11	chr2:211036478-211036528	GM12891	blood:	n/a
12	chr2:211035530-211035580	T-47D	breast:	n/a
13	chr2:211036822-211036872	HRPEpiC	eye:	n/a
14	chr2:211036822-211036872	HRE	kidney:	n/a
15	chr2:211035422-211035472	MCF10A-Er-Src	breast:	n/a
16	chr2:211036478-211036528	GM12878	blood:	n/a
17	chr2:211035360-211035410	PrEC	prostate:	n/a
18	chr2:211036478-211036528	HCT-116	colon:	n/a
19	chr2:211035360-211035410	PANC-1	pancreas:	n/a
20	chr2:211036478-211036528	Hepatocyte	liver:	n/a
21	chr2:211036599-211036649	ovcar-3	ovarian:	n/a
22	chr2:211036230-211036280	GM12891	blood:	n/a
23	chr2:211036822-211036872	HCPEpiC	choroid plexus:	n/a
24	chr2:211035422-211035472	U87	brain:	n/a
25	chr2:211036309-211036359	BJ	skin:	n/a
26	chr2:211036478-211036528	HCF	heart:	n/a
27	chr2:211035530-211035580	NT2-D1	testis:	n/a
28	chr2:211035257-211035307	MCF10A-Er-Src	breast:	n/a
29	chr2:211035526-211035576	PANC-1	pancreas:	n/a
30	chr2:211035530-211035580	HIPEpiC	eye:	n/a
31	chr2:211036309-211036359	PrEC	prostate:	n/a
32	chr2:211035526-211035576	PFSK-1	brain:	n/a
33	chr2:211035526-211035576	HUVEC	blood vessel:	n/a
34	chr2:211035530-211035580	HCPEpiC	choroid plexus:	n/a
35	chr2:211035526-211035576	HEEpiC	esophagus:	n/a
36	chr2:211035526-211035576	CMK	blood:	n/a
37	chr2:211036599-211036649	Hepatocyte	liver:	n/a
38	chr2:211036309-211036359	ProgFib	skin:	n/a
39	chr2:211036822-211036872	IMR90	lung:	fetal
40	chr2:211036230-211036280	HCPEpiC	choroid plexus:	n/a
41	chr2:211035526-211035576	HCT-116	colon:	n/a
42	chr2:211035422-211035472	NB4	blood:	n/a
43	chr2:211035360-211035410	Hela-S3	cervix:	n/a
44	chr2:211036822-211036872	CMK	blood:	n/a
45	chr2:211035526-211035576	ProgFib	skin:	n/a
46	chr2:211035526-211035576	T-47D	breast:	n/a
47	chr2:211036478-211036528	AG10803	skin:	n/a
48	chr2:211036230-211036280	CMK	blood:	n/a
49	chr2:211036599-211036649	AG09319	gingival:	n/a
50	chr2:211036822-211036872	HPAEpiC	pulmonary alveolar:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:27226170..27226980-chr2:211035625..211036127,2	Hela-S3	cervix:
2	chr2:211035591..211036129-chr20:33865533..33866124,2	NB4	blood:
3	chr13:49821570..49822518-chr2:211035226..211035805,2	NB4	blood:
4	chr1:45987079..45988015-chr2:211035169..211036135,2	Hela-S3	cervix:
5	chr2:210813951..210816642-chr2:211034382..211037269,2	K562	blood:
6	chr2:210865937..210867928-chr2:211034610..211037287,3	MCF-7	breast:
7	chr2:208633171..208635747-chr2:211035528..211037623,2	MCF-7	breast:
8	chr2:211035339..211036285-chr7:130794370..130795172,2	Hela-S3	cervix:
9	chr2:210866819..210868675-chr2:211034282..211036994,3	K562	blood:
10	chr2:211034902..211035782-chr7:7221578..7222378,2	NB4	blood:
11	chr12:52445112..52445895-chr2:211035711..211036692,2	Hela-S3	cervix:
12	chr2:211035016..211035669-chr5:96038518..96039212,2	Hela-S3	cervix:
13	chr2:211032641..211035129-chr2:211036259..211038578,2	MCF-7	breast:
14	chr2:210866819..210870543-chr2:211034282..211037464,4	K562	blood:
15	chr19:16653137..16653875-chr2:211035395..211036127,2	Hela-S3	cervix:
16	chr2:210866282..210870548-chr2:211034114..211037570,6	MCF-7	breast:
17	chr1:6844290..6845119-chr2:211035227..211035905,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACADL-1	chr2:211035061-211035318	NONHSAT076669
2	lnc-ACADL-1	chr2:211034946-211035378	NONHSAT076668
3	lnc-RPE-2	chr2:211036242-211036553	ENSG00000231294.1

No data

Variant related genes	Relation type
KANSL1L	TF binding region
ENSG00000263530	TF binding region
ENSG00000231294	TF binding region
KANSL1L	CpG island
ENSG00000263530	CpG island
ENSG00000231294	CpG island
ENSG00000090273	chromatin interactions
ENSG00000237436	chromatin interactions
ENSG00000117450	chromatin interactions
ENSG00000163251	chromatin interactions
ENSG00000128585	chromatin interactions
ENSG00000106392	chromatin interactions
ENSG00000231721	chromatin interactions
ENSG00000144406	chromatin interactions
ENSG00000088298	chromatin interactions
ENSG00000197713	chromatin interactions
ENSG00000085872	chromatin interactions
ENSG00000102543	chromatin interactions
ENSG00000153113	chromatin interactions
ENSG00000198746	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000126005	chromatin interactions

Extended variants
information (count: 57 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:57 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150415852	chr2:211035266-211035267	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
2	rs115131201	chr2:211035279-211035280	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
3	rs371765699	chr2:211035369-211035370	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
4	rs552450463	chr2:211035380-211035381	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
5	rs145397290	chr2:211035419-211035420	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
6	rs35125543	chr2:211035425-211035426	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs554878088	chr2:211035471-211035472	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
8	rs191381775	chr2:211035486-211035487	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
9	rs533847810	chr2:211035541-211035542	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
10	rs181308452	chr2:211035555-211035556	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
11	rs367576362	chr2:211035583-211035584	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
12	rs553940332	chr2:211035601-211035602	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
13	rs576897698	chr2:211035608-211035609	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
14	rs545860534	chr2:211035634-211035635	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
15	rs141465240	chr2:211035658-211035659	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
16	rs576266732	chr2:211035687-211035688	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
17	rs13013865	chr2:211035689-211035690	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
18	rs533350047	chr2:211035749-211035750	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
19	rs541980594	chr2:211035815-211035816	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
20	rs561711767	chr2:211035886-211035887	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
21	rs186002960	chr2:211035969-211035970	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
22	rs66917529	chr2:211036052-211036053	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
23	rs560264235	chr2:211036187-211036188	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs370438463	chr2:211036191-211036192	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs551765334	chr2:211036206-211036207	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs552165517	chr2:211036219-211036220	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs563165203	chr2:211036238-211036239	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs189672068	chr2:211036244-211036245	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
29	rs183475642	chr2:211036245-211036246	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
30	rs145091543	chr2:211036251-211036252	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
31	rs187742317	chr2:211036256-211036257	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
32	rs190959423	chr2:211036277-211036278	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
33	rs547512336	chr2:211036309-211036310	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
34	rs570565114	chr2:211036318-211036319	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
35	rs539397384	chr2:211036320-211036321	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
36	rs183538074	chr2:211036375-211036376	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
37	rs576017053	chr2:211036381-211036382	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
38	rs535371590	chr2:211036382-211036383	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
39	rs375525044	chr2:211036445-211036446	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
40	rs112419076	chr2:211036499-211036500	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
41	rs373119710	chr2:211036561-211036562	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs263676	chr2:211036635-211036636	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs71043977	chr2:211036719-211036720	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs398105261	chr2:211036732-211036733	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs571908827	chr2:211036768-211036769	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs540832269	chr2:211036790-211036791	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs530779538	chr2:211036823-211036824	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs560174642	chr2:211036829-211036830	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs116400914	chr2:211036839-211036840	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs528980338	chr2:211036844-211036845	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Renal cell carcinoma	18765545	CNVD
Ovarian cancer	19193619	CNVD
Non-small cell lung cancer	18676828	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Urothelial cell carcinoma	18451213	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:250 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:211033000-211038000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:211033200-211036800	Active TSS	Stomach Smooth Muscle	stomach
3	chr2:211033200-211037200	Active TSS	iPS-20b Cell Line	embryonic stem cell
4	chr2:211033200-211037400	Active TSS	Right Atrium	heart
5	chr2:211033200-211037800	Active TSS	Fetal Kidney	kidney
6	chr2:211033200-211037800	Active TSS	Thymus	Thymus
7	chr2:211033400-211036400	Active TSS	HMEC	breast
8	chr2:211033400-211037000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr2:211033400-211037200	Active TSS	GM12878-XiMat	blood
10	chr2:211033400-211037800	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr2:211033600-211035400	Flanking Active TSS	Primary hematopoietic stem cells	blood
12	chr2:211033600-211036800	Active TSS	Fetal Thymus	thymus
13	chr2:211033600-211037000	Active TSS	Fetal Brain Female	brain
14	chr2:211033600-211037200	Active TSS	Aorta	Aorta
15	chr2:211033600-211037400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr2:211033800-211035600	Active TSS	Brain Germinal Matrix	brain
17	chr2:211033800-211036800	Active TSS	Fetal Muscle Leg	muscle
18	chr2:211033800-211036800	Active TSS	K562	blood
19	chr2:211033800-211036800	Active TSS	NH-A	brain
20	chr2:211033800-211037200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr2:211033800-211037200	Active TSS	Ovary	ovary
22	chr2:211033800-211037400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr2:211033800-211037400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr2:211033800-211037400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr2:211033800-211037400	Active TSS	Psoas Muscle	Psoas
26	chr2:211033800-211037400	Active TSS	HSMMtube	muscle
27	chr2:211033800-211037600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr2:211034000-211036400	Active TSS	Cortex derived primary cultured neurospheres	brain
29	chr2:211034000-211036800	Active TSS	Muscle Satellite Cultured Cells	--
30	chr2:211034000-211036800	Active TSS	Brain Hippocampus Middle	brain
31	chr2:211034000-211036800	Active TSS	NHEK	skin
32	chr2:211034000-211036800	Active TSS	NHLF	lung
33	chr2:211034000-211037000	Active TSS	Brain Inferior Temporal Lobe	brain
34	chr2:211034000-211037000	Active TSS	Rectal Smooth Muscle	rectum
35	chr2:211034000-211037200	Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr2:211034000-211037400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr2:211034000-211037400	Active TSS	Skeletal Muscle Female	skeletal muscle
38	chr2:211034000-211037400	Active TSS	NHDF-Ad	bronchial
39	chr2:211034000-211037600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr2:211034000-211037800	Active TSS	HUES6 Cell Line	embryonic stem cell
41	chr2:211034200-211035400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr2:211034200-211036600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr2:211034200-211036800	Active TSS	Adipose Nuclei	Adipose
44	chr2:211034200-211036800	Active TSS	Fetal Stomach	stomach
45	chr2:211034200-211036800	Active TSS	Hela-S3	cervix
46	chr2:211034200-211036800	Active TSS	HUVEC	blood vessel
47	chr2:211034200-211037000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr2:211034200-211037000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr2:211034200-211037000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr2:211034200-211037000	Active TSS	Fetal Intestine Large	intestine

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