Variant report

Variant	nsv1044686
Chromosome Location	chr15:44489534-44697482
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2350)
CpG islands
(count:1098)
Chromatin interactive
region (count:63)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2350 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:44677230-44677411	K562	blood:	n/a	n/a
2	ARID3A	chr15:44582460-44582769	K562	blood:	n/a	n/a
3	ARID3A	chr15:44491625-44492037	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:44588847-44589771	K562	blood:	n/a	n/a
5	ATF1	chr15:44588868-44589726	K562	blood:	n/a	n/a
6	ATF2	chr15:44579948-44581069	GM12878	blood:	n/a	n/a
7	ATF2	chr15:44603317-44603674	GM12878	blood:	n/a	n/a
8	ATF2	chr15:44580114-44580921	GM12878	blood:	n/a	n/a
9	ATF2	chr15:44611541-44611946	GM12878	blood:	n/a	n/a
10	ATF2	chr15:44677030-44677438	GM12878	blood:	n/a	n/a
11	ATF2	chr15:44601703-44602208	GM12878	blood:	n/a	n/a
12	ATF2	chr15:44600451-44601424	GM12878	blood:	n/a	n/a
13	ATF2	chr15:44677174-44677854	GM12878	blood:	n/a	n/a
14	ATF2	chr15:44600385-44601563	GM12878	blood:	n/a	n/a
15	ATF2	chr15:44580665-44581088	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr15:44580687-44581155	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr15:44589246-44589694	K562	blood:	n/a	n/a
18	BACH1	chr15:44589308-44589788	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr15:44581980-44582042	K562	blood:	n/a	n/a
20	BACH1	chr15:44600194-44600250	K562	blood:	n/a	n/a
21	BACH1	chr15:44589205-44589741	K562	blood:	n/a	n/a
22	BACH1	chr15:44677223-44677573	K562	blood:	n/a	n/a
23	BACH1	chr15:44677390-44677496	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr15:44580469-44580936	GM12878	blood:	n/a	n/a
25	BATF	chr15:44589332-44589686	GM12878	blood:	n/a	chr15:44589502-44589513
26	BATF	chr15:44611620-44611972	GM12878	blood:	n/a	n/a
27	BATF	chr15:44601086-44601635	GM12878	blood:	n/a	n/a
28	BATF	chr15:44601085-44601411	GM12878	blood:	n/a	n/a
29	BATF	chr15:44677259-44677509	GM12878	blood:	n/a	chr15:44677404-44677415
30	BATF	chr15:44600509-44601056	GM12878	blood:	n/a	n/a
31	BATF	chr15:44600545-44600974	GM12878	blood:	n/a	n/a
32	BATF	chr15:44677285-44677584	GM12878	blood:	n/a	chr15:44677404-44677415
33	BCL11A	chr15:44600601-44601015	GM12878	blood:	n/a	n/a
34	BCL11A	chr15:44580353-44580910	GM12878	blood:	n/a	n/a
35	BCL11A	chr15:44600611-44600896	GM12878	blood:	n/a	n/a
36	BCL11A	chr15:44601085-44601422	GM12878	blood:	n/a	n/a
37	BCL11A	chr15:44677234-44677511	GM12878	blood:	n/a	n/a
38	BCL3	chr15:44600529-44601008	GM12878	blood:	n/a	n/a
39	BCL3	chr15:44600545-44600963	GM12878	blood:	n/a	n/a
40	BCL3	chr15:44580451-44581050	A549	lung:	n/a	n/a
41	BCL3	chr15:44580490-44580994	A549	lung:	n/a	n/a
42	BCLAF1	chr15:44611541-44612118	GM12878	blood:	n/a	n/a
43	BCLAF1	chr15:44677158-44677627	GM12878	blood:	n/a	n/a
44	BCLAF1	chr15:44600394-44601426	GM12878	blood:	n/a	n/a
45	BCLAF1	chr15:44580140-44581155	GM12878	blood:	n/a	chr15:44581038-44581051
46	BCLAF1	chr15:44579725-44581201	GM12878	blood:	n/a	chr15:44581038-44581051
47	BHLHE40	chr15:44579845-44581534	K562	blood:	n/a	chr15:44581179-44581195
48	BHLHE40	chr15:44611640-44611889	GM12878	blood:	n/a	n/a
49	BHLHE40	chr15:44588738-44589733	K562	blood:	n/a	n/a
50	BHLHE40	chr15:44579916-44581330	GM12878	blood:	n/a	chr15:44581179-44581195

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:44584673-44584723	NB4	blood:	n/a
2	chr15:44617767-44617817	AG04449	skin:	fetal
3	chr15:44580973-44581023	SAEC	small airway:	n/a
4	chr15:44580973-44581023	Jurkat	blood:	n/a
5	chr15:44584673-44584723	CMK	blood:	n/a
6	chr15:44584673-44584723	K562	blood:	n/a
7	chr15:44581013-44581063	IMR90	lung:	fetal
8	chr15:44580973-44581023	NH-A	brain:	n/a
9	chr15:44491027-44491077	Caco-2	colon:	n/a
10	chr15:44580973-44581023	Hepatocyte	liver:	n/a
11	chr15:44580517-44580567	A549	lung:	n/a
12	chr15:44581013-44581063	HAEpiC	amniotic membrane:	n/a
13	chr15:44584673-44584723	HAEpiC	amniotic membrane:	n/a
14	chr15:44581013-44581063	AG09309	skin:	n/a
15	chr15:44617767-44617817	BE2_C	brain:	n/a
16	chr15:44580143-44580193	AG10803	skin:	n/a
17	chr15:44581216-44581266	ProgFib	skin:	n/a
18	chr15:44617767-44617817	RPTEC	kidney:	n/a
19	chr15:44580192-44580242	H1-hESC	embryonic stem cell:	embryo
20	chr15:44617767-44617817	BJ	skin:	n/a
21	chr15:44580831-44580881	AG10803	skin:	n/a
22	chr15:44491027-44491077	GM19239	blood:	n/a
23	chr15:44491027-44491077	HIPEpiC	eye:	n/a
24	chr15:44580192-44580242	GM12891	blood:	n/a
25	chr15:44581430-44581480	HRPEpiC	eye:	n/a
26	chr15:44491027-44491077	GM12878	blood:	n/a
27	chr15:44581614-44581664	HIPEpiC	eye:	n/a
28	chr15:44580517-44580567	Caco-2	colon:	n/a
29	chr15:44581013-44581063	AG10803	skin:	n/a
30	chr15:44581614-44581664	ProgFib	skin:	n/a
31	chr15:44580973-44581023	BE2_C	brain:	n/a
32	chr15:44584673-44584723	HCF	heart:	n/a
33	chr15:44491027-44491077	SK-N-MC	brain:	n/a
34	chr15:44580517-44580567	AG10803	skin:	n/a
35	chr15:44580831-44580881	HRPEpiC	eye:	n/a
36	chr15:44580192-44580242	ECC-1	luminal epithelium:	n/a
37	chr15:44581614-44581664	GM12892	blood:	n/a
38	chr15:44617767-44617817	PrEC	prostate:	n/a
39	chr15:44581430-44581480	AoSMC	blood vessel:	n/a
40	chr15:44581614-44581664	GM12891	blood:	n/a
41	chr15:44584673-44584723	GM06990	blood:	n/a
42	chr15:44588704-44588754	HUVEC	blood vessel:	n/a
43	chr15:44581430-44581480	ECC-1	luminal epithelium:	n/a
44	chr15:44581311-44581361	HIPEpiC	eye:	n/a
45	chr15:44580545-44580595	SAEC	small airway:	n/a
46	chr15:44581430-44581480	K562	blood:	n/a
47	chr15:44581216-44581266	IMR90	lung:	fetal
48	chr15:44581430-44581480	SAEC	small airway:	n/a
49	chr15:44617767-44617817	ECC-1	luminal epithelium:	n/a
50	chr15:44544385-44544435	HIPEpiC	eye:	n/a

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:44580040..44582785-chr15:44587242..44592291,5	K562	blood:
2	chr15:44498063..44499784-chr15:44504783..44507604,2	MCF-7	breast:
3	chr15:44580146..44582349-chr15:44827451..44829460,2	MCF-7	breast:
4	chr15:44580352..44582378-chr15:44719445..44721367,2	MCF-7	breast:
5	chr15:44588053..44590579-chr15:44719354..44720991,3	K562	blood:
6	chr15:44192068..44194069-chr15:44510547..44512771,2	K562	blood:
7	chr15:44598927..44601826-chr15:44602549..44604440,2	K562	blood:
8	chr15:44579788..44582534-chr15:44587472..44590995,5	K562	blood:
9	chr15:44195722..44196644-chr15:44511206..44512558,6	MCF-7	breast:
10	chr15:44562480..44564339-chr15:44827596..44829843,2	K562	blood:
11	chr1:160626224..160626724-chr15:44580372..44580873,2	NB4	blood:
12	chr15:44578896..44580532-chr15:44718300..44720139,2	K562	blood:
13	chr15:44580463..44582588-chr15:44587860..44590321,2	MCF-7	breast:
14	chr15:44598749..44601264-chr15:44602549..44605810,3	K562	blood:
15	chr15:44560203..44561819-chr15:44573473..44575592,2	K562	blood:
16	chr15:44164813..44165436-chr15:44511999..44512879,2	MCF-7	breast:
17	chr15:44674181..44676932-chr15:44716918..44719048,2	K562	blood:
18	chr15:44597254..44598879-chr15:44647094..44649629,2	K562	blood:
19	chr15:44575170..44577372-chr15:44579582..44581514,2	K562	blood:
20	chr15:44587861..44590547-chr15:44741463..44744452,2	K562	blood:
21	chr15:44580195..44580716-chr19:49375247..49375759,2	Hela-S3	cervix:
22	chr15:44589031..44591213-chr15:44594276..44597075,2	K562	blood:
23	chr15:44600099..44602547-chr15:44607758..44609414,2	K562	blood:
24	chr15:44486877..44488833-chr15:44490905..44493302,2	MCF-7	breast:
25	chr15:44586214..44590579-chr15:44718275..44720991,4	K562	blood:
26	chr15:44572994..44575199-chr15:44578714..44581258,3	K562	blood:
27	chr15:44641156..44643504-chr15:44646406..44648886,2	K562	blood:
28	chr15:44579746..44580523-chr17:2310254..2310863,2	Hela-S3	cervix:
29	chr15:44627409..44629841-chr15:44832460..44835215,2	MCF-7	breast:
30	chr15:44566884..44569182-chr15:44579159..44580802,2	K562	blood:
31	chr15:44566884..44569182-chr15:44579159..44580802,2	K562	blood:
32	chr15:44643947..44646779-chr15:44717762..44720215,2	MCF-7	breast:
33	chr15:44580463..44582588-chr15:44587860..44590321,2	MCF-7	breast:
34	chr15:44607871..44610243-chr15:44613499..44616382,2	MCF-7	breast:
35	chr15:44498063..44499784-chr15:44504783..44507604,2	MCF-7	breast:
36	chr15:44673967..44676346-chr15:44716009..44718980,2	K562	blood:
37	chr15:44195949..44196699-chr15:44511446..44512539,4	K562	blood:
38	chr15:44496752..44498344-chr15:44833726..44836502,2	K562	blood:
39	chr15:44574254..44576946-chr15:44577393..44580315,2	MCF-7	breast:
40	chr15:44583396..44585705-chr15:44587497..44589558,5	K562	blood:
41	chr15:44588603..44589492-chr17:46184283..46185215,2	HCT-116	colon:
42	chr15:44537043..44539547-chr15:44542219..44544555,2	K562	blood:
43	chr15:44505864..44508334-chr15:44517714..44520133,2	K562	blood:
44	chr15:44580040..44582785-chr15:44587242..44592291,5	K562	blood:
45	chr15:44579788..44582534-chr15:44587472..44590995,5	K562	blood:
46	chr15:44557630..44559564-chr15:44579720..44582222,2	MCF-7	breast:
47	chr15:44583396..44585705-chr15:44587497..44589558,5	K562	blood:
48	chr15:44597254..44598879-chr15:44647094..44649629,2	K562	blood:
49	chr15:44600099..44602547-chr15:44607758..44609414,2	K562	blood:
50	chr15:44562480..44565823-chr15:44827596..44830231,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTDSPL2-5	chr15:44674277-44674427	NONHSAT042149
2	lnc-FRMD5-3	chr15:44580381-44580671	NONHSAT042139
3	lnc-CTDSPL2-5	chr15:44673062-44673174	NONHSAT042149
4	lnc-SPG11-4	chr15:44682164-44682649	ENSG00000259499.1
5	lnc-FRMD5-3	chr15:44567336-44567612	NONHSAT042139
6	lnc-FRMD5-1	chr15:44580909-44581263	ENSG00000259653.1
7	lnc-FRMD5-1	chr15:44581342-44581413	ENSG00000259653.1
8	lnc-SPG11-3	chr15:44694883-44695137	ENSG00000259595.1
9	lnc-SPG11-4	chr15:44679518-44679686	ENSG00000259499.1

No data

Variant related genes	Relation type
ENSG00000203574	TF binding region
ENSG00000203576	TF binding region
ENSG00000203572	TF binding region
CASC4	TF binding region
ENSG00000259499	TF binding region
ENSG00000203411	TF binding region
FRMD5	TF binding region
ENSG00000203578	TF binding region
ENSG00000196274	TF binding region
ENSG00000203573	TF binding region
ENSG00000203575	TF binding region
ENSG00000250130	TF binding region
ENSG00000203574	CpG island
ENSG00000203576	CpG island
ENSG00000203572	CpG island
CASC4	CpG island
ENSG00000259499	CpG island
ENSG00000203411	CpG island
FRMD5	CpG island
ENSG00000203578	CpG island
ENSG00000196274	CpG island
ENSG00000203573	CpG island
ENSG00000203575	CpG island
ENSG00000250130	CpG island
ENSG00000203575	chromatin interactions
ENSG00000250130	chromatin interactions
ENSG00000196274	chromatin interactions
ENSG00000104131	chromatin interactions
ENSG00000179523	chromatin interactions
ENSG00000171877	chromatin interactions
ENSG00000087074	chromatin interactions
ENSG00000203573	chromatin interactions
ENSG00000259595	chromatin interactions
ENSG00000002919	chromatin interactions
ENSG00000203576	chromatin interactions
ENSG00000137770	chromatin interactions
ENSG00000259335	chromatin interactions
ENSG00000203572	chromatin interactions
ENSG00000203574	chromatin interactions
ENSG00000166734	chromatin interactions

Extended variants
information (count: 6121 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:6121 , 50 per page) page: 1 2 3 4 5 6 7 ... 123

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs193143070	chr15:44489547-44489548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs561397023	chr15:44489568-44489569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554924453	chr15:44489608-44489609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540797731	chr15:44489625-44489626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs2615301	chr15:44489637-44489638	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs534018700	chr15:44489648-44489649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs554007745	chr15:44489687-44489688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150032230	chr15:44489737-44489738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144710114	chr15:44489762-44489763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs144971763	chr15:44489780-44489781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182836343	chr15:44489807-44489808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200387193	chr15:44489876-44489877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs5812271	chr15:44489877-44489878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575574095	chr15:44489892-44489893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562268148	chr15:44489893-44489894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs398043225	chr15:44489896-44489897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs377633738	chr15:44489897-44489898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529545243	chr15:44489913-44489914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544156091	chr15:44489942-44489943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561252392	chr15:44489943-44489944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530317583	chr15:44489952-44489953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540470772	chr15:44489972-44489973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560457176	chr15:44490050-44490051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532268079	chr15:44490127-44490128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs74595172	chr15:44490130-44490131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568905631	chr15:44490172-44490173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187272581	chr15:44490213-44490214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs2696077	chr15:44490239-44490240	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs568411356	chr15:44490261-44490262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372800726	chr15:44490276-44490277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564213987	chr15:44490344-44490345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372390172	chr15:44490345-44490346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534059456	chr15:44490368-44490369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554044611	chr15:44490383-44490384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541471114	chr15:44490416-44490417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs149046363	chr15:44490449-44490450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs117360557	chr15:44490457-44490458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544237463	chr15:44490518-44490519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554537842	chr15:44490522-44490523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373959676	chr15:44490524-44490525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs61186028	chr15:44490525-44490526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574818802	chr15:44490541-44490542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540507847	chr15:44490542-44490543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560802166	chr15:44490548-44490549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577388158	chr15:44490551-44490552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546330570	chr15:44490571-44490572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs76907701	chr15:44490583-44490584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562484462	chr15:44490584-44490585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369542732	chr15:44490614-44490615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76209737	chr15:44490700-44490701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Mental retardation	17124404	CNVD
Melanoma	17363583	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2569 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:44488000-44491400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr15:44488000-44491600	Weak transcription	Pancreas	Pancrea
3	chr15:44488000-44491600	Weak transcription	Spleen	Spleen
4	chr15:44488200-44491000	Weak transcription	Fetal Brain Male	brain
5	chr15:44488200-44491200	Weak transcription	NHEK	skin
6	chr15:44488200-44491400	Weak transcription	Hela-S3	cervix
7	chr15:44488200-44491400	Weak transcription	HMEC	breast
8	chr15:44488200-44491400	Weak transcription	HUVEC	blood vessel
9	chr15:44488200-44491600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr15:44488200-44491600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr15:44488200-44491600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr15:44488200-44492600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr15:44488200-44492600	Weak transcription	Brain Hippocampus Middle	brain
14	chr15:44488400-44491400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr15:44488400-44491600	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr15:44490600-44491000	Weak transcription	HepG2	liver
17	chr15:44491000-44492600	Enhancers	HepG2	liver
18	chr15:44491200-44491400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr15:44491200-44492200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr15:44491200-44492200	Enhancers	Stomach Mucosa	stomach
21	chr15:44491200-44492200	Enhancers	NHEK	skin
22	chr15:44491200-44493000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr15:44491400-44491600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr15:44491400-44491800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr15:44491400-44492000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr15:44491400-44492000	Enhancers	HMEC	breast
27	chr15:44491400-44492200	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr15:44491400-44492200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr15:44491400-44492200	Enhancers	Hela-S3	cervix
30	chr15:44491400-44492200	Enhancers	HUVEC	blood vessel
31	chr15:44491600-44491800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr15:44491600-44492000	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr15:44491600-44492000	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr15:44491600-44492000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr15:44491600-44492000	Enhancers	Pancreas	Pancrea
36	chr15:44491600-44492000	Enhancers	Spleen	Spleen
37	chr15:44491600-44492200	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr15:44491600-44492200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr15:44492000-44493600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr15:44492600-44493000	Enhancers	Brain Hippocampus Middle	brain
41	chr15:44492600-44493400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr15:44496200-44496800	Enhancers	Brain Germinal Matrix	brain
43	chr15:44499400-44499800	Enhancers	HUVEC	blood vessel
44	chr15:44499400-44499800	Enhancers	NHEK	skin
45	chr15:44499400-44500000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr15:44499400-44500400	Enhancers	HMEC	breast
47	chr15:44499600-44499800	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr15:44499600-44500000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr15:44499600-44500200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr15:44499600-44500200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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