Variant report

Variant	esv1801752
Chromosome Location	chr2:87245762-88123177
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:9708)
CpG islands
(count:1649)
Chromatin interactive
region (count:9)
LncRNA
region (count:55)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:9708 , 50 per page) page: 1 2 3 4 5 6 7 ... 195

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:87842112-87842471	K562	blood:	n/a	n/a
2	ARID3A	chr2:87623758-87624080	K562	blood:	n/a	n/a
3	ARID3A	chr2:87832053-87832224	K562	blood:	n/a	n/a
4	ARID3A	chr2:87765959-87766268	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:87623772-87624052	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:87795618-87796003	K562	blood:	n/a	n/a
7	ARID3A	chr2:87929041-87929371	K562	blood:	n/a	n/a
8	ARID3A	chr2:87799487-87800222	K562	blood:	n/a	n/a
9	ARID3A	chr2:87812449-87812709	HepG2	liver:	n/a	n/a
10	ARID3A	chr2:87802514-87802706	K562	blood:	n/a	n/a
11	ARID3A	chr2:87816067-87816298	K562	blood:	n/a	n/a
12	ARID3A	chr2:87797922-87797977	K562	blood:	n/a	n/a
13	ARID3A	chr2:87903474-87903688	K562	blood:	n/a	n/a
14	ATF1	chr2:87568829-87569093	K562	blood:	n/a	n/a
15	ATF1	chr2:87816074-87816451	K562	blood:	n/a	n/a
16	ATF1	chr2:87756399-87756603	K562	blood:	n/a	n/a
17	ATF1	chr2:87303415-87304067	K562	blood:	n/a	n/a
18	ATF1	chr2:87741013-87741231	K562	blood:	n/a	n/a
19	ATF1	chr2:87754798-87755008	K562	blood:	n/a	n/a
20	ATF1	chr2:87929184-87929384	K562	blood:	n/a	n/a
21	ATF1	chr2:87842104-87842488	K562	blood:	n/a	n/a
22	ATF1	chr2:87903372-87903674	K562	blood:	n/a	n/a
23	ATF1	chr2:87883958-87884458	K562	blood:	n/a	n/a
24	ATF1	chr2:87794523-87794820	K562	blood:	n/a	n/a
25	ATF2	chr2:87770617-87770892	GM12878	blood:	n/a	n/a
26	ATF2	chr2:87770596-87770855	GM12878	blood:	n/a	n/a
27	ATF3	chr2:87623739-87624043	A549	lung:	n/a	n/a
28	ATF3	chr2:87903447-87903666	K562	blood:	n/a	n/a
29	BACH1	chr2:87770563-87770872	K562	blood:	n/a	n/a
30	BACH1	chr2:87929012-87929445	H1-hESC	embryonic stem cell:	n/a	chr2:87929136-87929150
31	BACH1	chr2:87776227-87776422	K562	blood:	n/a	n/a
32	BACH1	chr2:87928999-87929447	K562	blood:	n/a	chr2:87929136-87929150
33	BACH1	chr2:87754799-87755006	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr2:87623757-87624094	K562	blood:	n/a	n/a
35	BATF	chr2:87957934-87958163	GM12878	blood:	n/a	n/a
36	BATF	chr2:87811814-87812101	GM12878	blood:	n/a	n/a
37	BATF	chr2:87303340-87303849	GM12878	blood:	n/a	n/a
38	BATF	chr2:87552193-87552541	GM12878	blood:	n/a	chr2:87552384-87552395 chr2:87552385-87552395
39	BATF	chr2:87560256-87560538	GM12878	blood:	n/a	n/a
40	BATF	chr2:87754517-87755693	GM12878	blood:	n/a	n/a
41	BATF	chr2:87742677-87743205	GM12878	blood:	n/a	n/a
42	BATF	chr2:87540572-87540863	GM12878	blood:	n/a	chr2:87540719-87540729 chr2:87540723-87540733 chr2:87540722-87540733
43	BATF	chr2:87824077-87824693	GM12878	blood:	n/a	n/a
44	BATF	chr2:87930390-87930714	GM12878	blood:	n/a	n/a
45	BATF	chr2:87933631-87933945	GM12878	blood:	n/a	n/a
46	BATF	chr2:87740183-87740443	GM12878	blood:	n/a	n/a
47	BATF	chr2:87813339-87814035	GM12878	blood:	n/a	chr2:87813652-87813660
48	BATF	chr2:87299212-87299437	GM12878	blood:	n/a	n/a
49	BATF	chr2:87848684-87848919	GM12878	blood:	n/a	chr2:87848684-87848694 chr2:87848797-87848808
50	BATF	chr2:87978157-87978497	GM12878	blood:	n/a	chr2:87978353-87978364

(count:1649 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:87569447-87569497	HPAEpiC	pulmonary alveolar:	n/a
2	chr2:87576370-87576420	ProgFib	skin:	n/a
3	chr2:87569447-87569497	HPAEpiC	pulmonary alveolar:	n/a
4	chr2:87576370-87576420	ProgFib	skin:	n/a
5	chr2:87576399-87576449	NHBE	bronchial:	n/a
6	chr2:87420273-87420323	HEEpiC	esophagus:	n/a
7	chr2:87304015-87304065	NHBE	bronchial:	n/a
8	chr2:87308486-87308536	Jurkat	blood:	n/a
9	chr2:87445161-87445211	HAEpiC	amniotic membrane:	n/a
10	chr2:87304894-87304944	HRPEpiC	eye:	n/a
11	chr2:87572542-87572592	AG04450	lung:	fetal
12	chr2:87572542-87572592	HUVEC	blood vessel:	n/a
13	chr2:87420273-87420323	HAEpiC	amniotic membrane:	n/a
14	chr2:87302162-87302212	NH-A	brain:	n/a
15	chr2:87304015-87304065	AG09309	skin:	n/a
16	chr2:87302855-87302905	SAEC	small airway:	n/a
17	chr2:87755371-87755421	AG09319	gingival:	n/a
18	chr2:87302162-87302212	Hela-S3	cervix:	n/a
19	chr2:87569142-87569192	SK-N-SH	brain:	n/a
20	chr2:87304894-87304944	SK-N-SH_RA	brain:	n/a
21	chr2:87303632-87303682	HCF	heart:	n/a
22	chr2:87420273-87420323	IMR90	lung:	fetal
23	chr2:87302643-87302693	GM06990	blood:	n/a
24	chr2:87302162-87302212	GM12891	blood:	n/a
25	chr2:87755371-87755421	HRE	kidney:	n/a
26	chr2:87302643-87302693	IMR90	lung:	fetal
27	chr2:87305913-87305963	SKMC	muscle:	n/a
28	chr2:87568958-87569008	GM12892	blood:	n/a
29	chr2:87305913-87305963	U87	brain:	n/a
30	chr2:87569142-87569192	HEK293	kidney:	embryo
31	chr2:87304197-87304247	ovcar-3	ovarian:	n/a
32	chr2:87566763-87566813	HEEpiC	esophagus:	n/a
33	chr2:87302162-87302212	SAEC	small airway:	n/a
34	chr2:87566763-87566813	GM19239	blood:	n/a
35	chr2:87304105-87304155	HPAEpiC	pulmonary alveolar:	n/a
36	chr2:87445161-87445211	NHDF-neo	bronchial:	n/a
37	chr2:87566763-87566813	HL-60	blood:	n/a
38	chr2:87304197-87304247	MCF10A-Er-Src	breast:	n/a
39	chr2:87308486-87308536	SK-N-SH_RA	brain:	n/a
40	chr2:87576370-87576420	PFSK-1	brain:	n/a
41	chr2:87569275-87569325	HIPEpiC	eye:	n/a
42	chr2:87575991-87576041	NH-A	brain:	n/a
43	chr2:87568958-87569008	PFSK-1	brain:	n/a
44	chr2:87755371-87755421	AG04449	skin:	fetal
45	chr2:87302162-87302212	HepG2	liver:	n/a
46	chr2:87572542-87572592	HMEC	breast:	n/a
47	chr2:87576399-87576449	HRPEpiC	eye:	n/a
48	chr2:87445161-87445211	AG04449	skin:	fetal
49	chr2:87883547-87883597	SK-N-MC	brain:	n/a
50	chr2:88054543-88054593	GM12878	blood:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:87794607..87797367-chr2:88315602..88317365,2	K562	blood:
2	chr2:87281176..87283798-chr2:87302577..87304633,2	MCF-7	breast:
3	chr2:86789024..86791664-chr2:87302659..87304185,2	MCF-7	breast:
4	chr2:87281176..87283798-chr2:87302577..87304633,2	MCF-7	breast:
5	chr2:87472406..87474648-chr2:112477037..112478664,2	MCF-7	breast:
6	chr2:87431267..87434250-chr2:112516766..112518517,2	MCF-7	breast:
7	chr2:87813553..87816546-chr2:111876759..111878642,2	MCF-7	breast:
8	chr1:149222733..149224997-chr2:87623931..87625447,2	K562	blood:
9	chr2:87444854..87445468-chr2:112505392..112505911,4	MCF-7	breast:

(count:55 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SMYD1-6	chr2:88053047-88053153	NONHSAT072164
2	lnc-CD8B-3	chr2:87244676-87245831	NONHSAT072124
3	lnc-PLGLB1-3	chr2:87403979-87404208	l_1879_chr2:87403978-87405069_thyroid
4	lnc-PLGLB2-1	chr2:87769469-87769561	ENSG00000222041
5	lnc-PLGLB1-3	chr2:87404223-87404330	l_1879_chr2:87403978-87405069_thyroid
6	lnc-RGPD2-3	chr2:87777014-87777553	ENSG00000273445.1
7	lnc-PLGLB1-3	chr2:87405044-87405069	l_1879_chr2:87403978-87405069_thyroid
8	lnc-PLGLB2-1	chr2:87754974-87755164	NONHSAT072145
9	lnc-PLGLB2-1	chr2:87769669-87769823	ENSG00000222041
10	lnc-PLGLB2-1	chr2:87755024-87755164	ENSG00000222041
11	lnc-PLGLB2-1	chr2:87820726-87821030	NONHSAT072150
12	lnc-PLGLB2-1	chr2:87777641-87777749	NONHSAT072146
13	lnc-PLGLB2-1	chr2:87880503-87880765	ENSG00000222041.6
14	lnc-PLGLB2-1	chr2:87820726-87821030	NONHSAT072145
15	lnc-PLGLB1-4	chr2:87448236-87449611	NONHSAT072131
16	lnc-PLGLB2-1	chr2:87779742-87780211	ENSG00000222041
17	lnc-PLGLB2-1	chr2:87769669-87769823	ENSG00000222041
18	lnc-PLGLB2-1	chr2:87772259-87772404	NONHSAT072145
19	lnc-PLGLB2-1	chr2:87769669-87769823	NONHSAT072150
20	lnc-SMYD1-6	chr2:88056339-88057152	NONHSAT072164
21	lnc-RGPD1-5	chr2:87601841-87602143	ucscGeneNc_uc010fgz_1
22	lnc-PLGLB2-1	chr2:87772259-87772404	ENSG00000222041
23	lnc-PLGLB2-1	chr2:87820726-87821030	NR_024206
24	lnc-RGPD1-4	chr2:87596356-87596632	NONHSAT072140
25	lnc-PLGLB2-1	chr2:87777641-87777749	ENSG00000222041
26	lnc-PLGLB1-5	chr2:87539491-87539624	l_1881_chr2:87520157-87539624_76bGuttman_hLF
27	lnc-PLGLB2-1	chr2:87754998-87755164	ENSG00000222041
28	lnc-RGPD1-2	chr2:87528781-87529374	NONHSAT072132
29	lnc-PLGLB2-1	chr2:87882777-87883000	ENSG00000222041.6
30	lnc-PLGLB2-1	chr2:87882777-87882848	NONHSAT072150
31	lnc-RGPD2-1	chr2:87865347-87866283	NONHSAT072155
32	lnc-PLGLB2-1	chr2:87755015-87755164	ENSG00000222041
33	lnc-PLGLB2-1	chr2:87779742-87779914	NONHSAT072150
34	lnc-PLGLB2-1	chr2:87772259-87772404	ENSG00000222041
35	lnc-PLGLB2-1	chr2:87820726-87821030	NONHSAT072146
36	lnc-PLGLB1-5	chr2:87520158-87520527	l_1881_chr2:87520157-87539624_76bGuttman_hLF
37	lnc-PLGLB2-1	chr2:87755094-87755164	NONHSAT072150
38	lnc-PLGLB2-1	chr2:87755061-87755164	ENSG00000222041
39	lnc-SMYD1-6	chr2:88050746-88051901	NONHSAT072164
40	lnc-PLGLB2-1	chr2:87779742-87779942	ENSG00000222041
41	lnc-PLGLB2-3	chr2:88038283-88038784	NONHSAT072160
42	lnc-SMYD1-1	chr2:88047115-88047354	XLOC_001560
43	lnc-SMYD1-1	chr2:88045926-88046000	XLOC_001560
44	lnc-PLGLB2-1	chr2:87820726-87820932	ENSG00000222041
45	lnc-RGPD1-5	chr2:87536124-87536279	ucscGeneNc_uc010fgz_1
46	lnc-PLGLB2-6	chr2:87954409-87954762	NONHSAT072157
47	lnc-PLGLB2-1	chr2:87820726-87820932	ENSG00000222041
48	lnc-PLGLB2-1	chr2:87754974-87755164	NONHSAT072146
49	lnc-PLGLB2-1	chr2:87754974-87755164	NR_024206
50	lnc-PLGLB2-1	chr2:87779742-87780126	ENSG00000222041

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4435	chr2:87929283-87929304	MIMAT0018951
hsa-miR-4771	chr2:87421953-87421973	MIMAT0019925

No data

Variant related genes	Relation type
ENSG00000234231	TF binding region
IGKV3OR2-268	TF binding region
ENSG00000214354	TF binding region
ENSG00000266931	TF binding region
MIR4771-2	TF binding region
ENSG00000231259	TF binding region
ENSG00000225049	TF binding region
PLGLB1	TF binding region
MTATP8P2	TF binding region
MIR4435-1	TF binding region
PLGLB2	TF binding region
ENSG00000273445	TF binding region
ENSG00000213375	TF binding region
ENSG00000224881	TF binding region
LINC00152	TF binding region
ENSG00000225933	TF binding region
RGPD2	TF binding region
ENSG00000230395	TF binding region
ENSG00000204745	TF binding region
ENSG00000271097	TF binding region
ENSG00000233671	TF binding region
ENSG00000234231	CpG island
IGKV3OR2-268	CpG island
ENSG00000214354	CpG island
ENSG00000266931	CpG island
MIR4771-2	CpG island
ENSG00000231259	CpG island
ENSG00000225049	CpG island
PLGLB1	CpG island
MTATP8P2	CpG island
MIR4435-1	CpG island
PLGLB2	CpG island
ENSG00000273445	CpG island
ENSG00000213375	CpG island
ENSG00000224881	CpG island
LINC00152	CpG island
ENSG00000225933	CpG island
RGPD2	CpG island
ENSG00000230395	CpG island
ENSG00000204745	CpG island
ENSG00000271097	CpG island
ENSG00000233671	CpG island
ENSG00000231259	chromatin interactions
ENSG00000266931	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000115561	chromatin interactions
ENSG00000222724	chromatin interactions
ENSG00000153094	chromatin interactions
ENSG00000228363	chromatin interactions
GLT25D1	miRNA target sites
GNA13	miRNA target sites

Extended variants
information (count: 13580 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:13580 , 50 per page) page: 1 2 3 4 5 6 7 ... 272

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554255160	chr2:87246170-87246171	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs377440834	chr2:87246194-87246195	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs567184425	chr2:87246222-87246223	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs370594996	chr2:87246237-87246238	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs377236677	chr2:87246241-87246242	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs2138304	chr2:87246280-87246281	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs534223188	chr2:87246485-87246486	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs558766876	chr2:87246491-87246492	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs577034024	chr2:87246518-87246519	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs544354263	chr2:87246578-87246579	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs200611872	chr2:87246586-87246587	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs201581110	chr2:87246609-87246610	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs62148342	chr2:87246686-87246687	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs367587311	chr2:87248068-87248069	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs371464997	chr2:87248101-87248102	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs528429856	chr2:87248111-87248112	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs540521478	chr2:87248186-87248187	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs565134790	chr2:87248320-87248321	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs532348860	chr2:87248350-87248351	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs550762636	chr2:87248367-87248368	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs569010023	chr2:87248429-87248430	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs529735224	chr2:87248451-87248452	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs112428780	chr2:87248461-87248462	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs566335227	chr2:87248788-87248789	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs533741962	chr2:87248840-87248841	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs558829030	chr2:87248903-87248904	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs570782885	chr2:87248917-87248918	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs62148344	chr2:87249059-87249060	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs538064050	chr2:87249134-87249135	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs556322041	chr2:87249139-87249140	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs574905386	chr2:87249163-87249164	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs541952652	chr2:87249225-87249226	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs111706611	chr2:87249335-87249336	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs529837635	chr2:87249993-87249994	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs547990104	chr2:87250006-87250007	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs560147888	chr2:87250065-87250066	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs527312170	chr2:87250154-87250155	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs551720833	chr2:87250181-87250182	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs570842246	chr2:87250194-87250195	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs374599737	chr2:87250455-87250456	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs377265548	chr2:87250456-87250457	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs539878902	chr2:87250493-87250494	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs201960583	chr2:87250506-87250507	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs200852497	chr2:87250521-87250522	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs372618449	chr2:87250540-87250541	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs577259460	chr2:87250685-87250686	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs544511754	chr2:87250739-87250740	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs562763051	chr2:87250740-87250741	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs574549619	chr2:87250783-87250784	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs541980428	chr2:87250795-87250796	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	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
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	18438408	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Williams Syndrome	20824207	CNVD
Type 1 diabetes	21085585	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:3839 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:87258800-87283200	Weak transcription	Fetal Intestine Small	intestine
2	chr2:87259200-87281600	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr2:87268600-87280600	Weak transcription	Colonic Mucosa	Colon
4	chr2:87271800-87277200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr2:87271800-87277600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:87271800-87282200	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr2:87275000-87277200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr2:87275200-87281000	Weak transcription	Primary B cells from peripheral blood	blood
9	chr2:87275200-87283000	Weak transcription	Fetal Muscle Leg	muscle
10	chr2:87275400-87277200	Weak transcription	Fetal Thymus	thymus
11	chr2:87275600-87277200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr2:87275600-87277200	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr2:87275600-87277400	Weak transcription	Dnd41	blood
14	chr2:87275600-87284000	Weak transcription	Fetal Stomach	stomach
15	chr2:87275600-87302000	Weak transcription	Duodenum Mucosa	Duodenum
16	chr2:87275800-87277400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr2:87276000-87277600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr2:87276000-87280800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr2:87276000-87281400	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr2:87276200-87278800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr2:87276200-87285200	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr2:87276400-87278800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr2:87276400-87282400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr2:87276400-87283400	Weak transcription	Fetal Muscle Trunk	muscle
25	chr2:87276400-87283800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr2:87276400-87285000	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr2:87276400-87295400	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr2:87276400-87295400	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr2:87276600-87283000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr2:87276600-87302000	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr2:87276800-87279400	Weak transcription	Hela-S3	cervix
32	chr2:87277000-87281000	Weak transcription	Brain Germinal Matrix	brain
33	chr2:87277200-87278000	Strong transcription	Primary monocytes fromperipheralblood	blood
34	chr2:87277200-87279200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr2:87277200-87279200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr2:87277200-87279200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr2:87277200-87279200	Strong transcription	Fetal Thymus	thymus
38	chr2:87277200-87279800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr2:87277200-87284800	Weak transcription	Thymus	Thymus
40	chr2:87277400-87279200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr2:87277400-87279200	Strong transcription	Dnd41	blood
42	chr2:87277600-87278200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr2:87277600-87279000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr2:87277600-87280600	Weak transcription	Fetal Lung	lung
45	chr2:87277800-87278000	Enhancers	Left Ventricle	heart
46	chr2:87277800-87280400	Weak transcription	Primary hematopoietic stem cells	blood
47	chr2:87277800-87287400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr2:87278000-87279400	Weak transcription	Left Ventricle	heart
49	chr2:87278000-87283800	Weak transcription	Primary monocytes fromperipheralblood	blood
50	chr2:87278200-87278600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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