Variant report

Variant	nsv570171
Chromosome Location	chr15:78064664-78131097
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1090)
CpG islands
(count:1101)
Chromatin interactive
region (count:64)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1090 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:78077195-78077543	K562	blood:	n/a	n/a
2	BACH1	chr15:78111596-78111934	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr15:78112581-78112794	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr15:78088304-78088829	GM12878	blood:	n/a	n/a
5	BCL3	chr15:78088327-78088760	GM12878	blood:	n/a	n/a
6	BHLHE40	chr15:78113211-78113483	K562	blood:	n/a	chr15:78113370-78113391 chr15:78113374-78113387
7	BHLHE40	chr15:78095857-78096131	K562	blood:	n/a	n/a
8	BHLHE40	chr15:78104173-78104542	K562	blood:	n/a	chr15:78104303-78104324 chr15:78104308-78104317 chr15:78104309-78104318 chr15:78104310-78104319 chr15:78104309-78104318 chr15:78104307-78104320
9	BHLHE40	chr15:78102084-78102117	K562	blood:	n/a	n/a
10	BHLHE40	chr15:78089629-78089938	GM12878	blood:	n/a	n/a
11	BHLHE40	chr15:78096532-78096945	K562	blood:	n/a	n/a
12	BHLHE40	chr15:78113815-78114121	K562	blood:	n/a	chr15:78113828-78113844
13	BHLHE40	chr15:78112561-78112947	K562	blood:	n/a	n/a
14	BHLHE40	chr15:78101148-78101512	HepG2	liver:	n/a	chr15:78101316-78101325 chr15:78101317-78101326 chr15:78101317-78101326
15	BHLHE40	chr15:78101143-78101495	K562	blood:	n/a	chr15:78101316-78101325 chr15:78101317-78101326 chr15:78101317-78101326
16	BHLHE40	chr15:78077441-78077584	K562	blood:	n/a	n/a
17	BRCA1	chr15:78116340-78116364	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr15:78077171-78077598	K562	blood:	n/a	n/a
19	CCNT2	chr15:78112531-78112910	K562	blood:	n/a	n/a
20	CEBPB	chr15:78097916-78098237	MCF-7	breast:	n/a	chr15:78098032-78098043
21	CEBPB	chr15:78097866-78098207	IMR90	lung:	n/a	chr15:78098032-78098043
22	CEBPB	chr15:78097908-78098155	H1-hESC	embryonic stem cell:	n/a	chr15:78098032-78098043
23	CEBPB	chr15:78097862-78098204	HepG2	liver:	n/a	chr15:78098032-78098043
24	CEBPB	chr15:78097872-78098202	A549	lung:	n/a	chr15:78098032-78098043
25	CEBPB	chr15:78077418-78077509	K562	blood:	n/a	n/a
26	CEBPB	chr15:78097972-78098198	Hela-S3	cervix:	n/a	chr15:78098032-78098043
27	CEBPB	chr15:78097885-78098211	K562	blood:	n/a	chr15:78098032-78098043
28	CHD1	chr15:78111718-78111742	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr15:78112731-78112878	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr15:78093119-78093139	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr15:78114017-78114116	K562	blood:	n/a	n/a
32	CHD2	chr15:78112768-78112882	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr15:78128582-78129087	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr15:78095843-78096168	K562	blood:	n/a	n/a
35	CHD2	chr15:78089582-78089843	GM12878	blood:	n/a	n/a
36	CHD2	chr15:78122597-78122722	Hela-S3	cervix:	n/a	n/a
37	CREB1	chr15:78112210-78112963	A549	lung:	n/a	n/a
38	CREB1	chr15:78077295-78077568	A549	lung:	n/a	n/a
39	CTBP2	chr15:78111581-78112011	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr15:78113920-78114070	AoAF	blood vessel:	n/a	chr15:78113982-78114000
41	CTCF	chr15:78113920-78114070	AG04450	lung:	n/a	chr15:78113982-78114000
42	CTCF	chr15:78077153-78077163	GM12892	blood:	n/a	n/a
43	CTCF	chr15:78077376-78077589	GM19239	blood:	n/a	n/a
44	CTCF	chr15:78113900-78114050	HRPEpiC	eye:	n/a	chr15:78113982-78114000
45	CTCF	chr15:78115780-78115930	BE2_C	brain:	n/a	n/a
46	CTCF	chr15:78112700-78112850	GM12870	blood:	n/a	chr15:78112771-78112781
47	CTCF	chr15:78114698-78114701	GM10266	blood:	n/a	n/a
48	CTCF	chr15:78113817-78114072	HepG2	liver:	n/a	chr15:78113982-78114000
49	CTCF	chr15:78112700-78112850	SAEC	small airway:	n/a	chr15:78112771-78112781
50	CTCF	chr15:78113940-78114090	NHDF-neo	bronchial:	n/a	chr15:78113982-78114000

(count:1101 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:78118816-78118866	AG04450	lung:	fetal
2	chr15:78112818-78112868	HNPCEpiC	eye:	n/a
3	chr15:78110857-78110907	ECC-1	luminal epithelium:	n/a
4	chr15:78118816-78118866	AG04450	lung:	fetal
5	chr15:78112818-78112868	HNPCEpiC	eye:	n/a
6	chr15:78110857-78110907	ECC-1	luminal epithelium:	n/a
7	chr15:78109450-78109500	SKMC	muscle:	n/a
8	chr15:78110857-78110907	HCPEpiC	choroid plexus:	n/a
9	chr15:78110106-78110156	Jurkat	blood:	n/a
10	chr15:78112026-78112076	SK-N-MC	brain:	n/a
11	chr15:78103228-78103278	AG10803	skin:	n/a
12	chr15:78103228-78103278	HRCEpiC	kidney:	n/a
13	chr15:78110903-78110953	HCM	heart:	n/a
14	chr15:78110106-78110156	PrEC	prostate:	n/a
15	chr15:78114278-78114328	HEEpiC	esophagus:	n/a
16	chr15:78110903-78110953	AG09319	gingival:	n/a
17	chr15:78112026-78112076	PrEC	prostate:	n/a
18	chr15:78112026-78112076	HCM	heart:	n/a
19	chr15:78111390-78111440	CMK	blood:	n/a
20	chr15:78112818-78112868	PANC-1	pancreas:	n/a
21	chr15:78077656-78077706	PANC-1	pancreas:	n/a
22	chr15:78113237-78113287	BJ	skin:	n/a
23	chr15:78110857-78110907	HUVEC	blood vessel:	n/a
24	chr15:78109450-78109500	T-47D	breast:	n/a
25	chr15:78112847-78112897	HUVEC	blood vessel:	n/a
26	chr15:78118816-78118866	AG09309	skin:	n/a
27	chr15:78110857-78110907	HRCEpiC	kidney:	n/a
28	chr15:78110106-78110156	HIPEpiC	eye:	n/a
29	chr15:78111196-78111246	SKMC	muscle:	n/a
30	chr15:78110903-78110953	HepG2	liver:	n/a
31	chr15:78114888-78114938	NB4	blood:	n/a
32	chr15:78103228-78103278	HRPEpiC	eye:	n/a
33	chr15:78111390-78111440	PFSK-1	brain:	n/a
34	chr15:78113237-78113287	BE2_C	brain:	n/a
35	chr15:78114888-78114938	HEK293	kidney:	embryo
36	chr15:78108562-78108612	U87	brain:	n/a
37	chr15:78110903-78110953	HRCEpiC	kidney:	n/a
38	chr15:78113237-78113287	Caco-2	colon:	n/a
39	chr15:78112026-78112076	BJ	skin:	n/a
40	chr15:78103228-78103278	NHBE	bronchial:	n/a
41	chr15:78111196-78111246	ECC-1	luminal epithelium:	n/a
42	chr15:78114278-78114328	HUVEC	blood vessel:	n/a
43	chr15:78110106-78110156	SKMC	muscle:	n/a
44	chr15:78112026-78112076	MCF-7	breast:	n/a
45	chr15:78113237-78113287	NHDF-neo	bronchial:	n/a
46	chr15:78112026-78112076	U87	brain:	n/a
47	chr15:78103228-78103278	GM12878	blood:	n/a
48	chr15:78111196-78111246	AG09309	skin:	n/a
49	chr15:78112847-78112897	IMR90	lung:	fetal
50	chr15:78112847-78112897	SK-N-SH	brain:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:78097465..78099114-chr15:78102921..78104806,2	K562	blood:
2	chr15:78103078..78104823-chr15:78106896..78108558,2	K562	blood:
3	chr15:78097066..78100710-chr15:78102142..78106147,5	K562	blood:
4	chr15:78093726..78095482-chr15:78109302..78111368,2	K562	blood:
5	chr15:77925249..77927257-chr15:78113205..78115049,24	MCF-7	breast:
6	chr15:78129825..78131680-chr15:78135529..78137556,2	K562	blood:
7	chr15:78099210..78100960-chr15:78102155..78104684,2	K562	blood:
8	chr15:78115466..78118484-chr15:78120011..78123409,3	MCF-7	breast:
9	chr15:78083797..78085667-chr15:78106019..78108853,2	K562	blood:
10	chr15:77950482..77951067-chr15:78113646..78114389,2	K562	blood:
11	chr15:78029999..78032267-chr15:78076792..78079270,2	MCF-7	breast:
12	chr15:78088888..78092011-chr15:78092368..78096073,3	K562	blood:
13	chr15:78107758..78109313-chr15:78111361..78113671,2	K562	blood:
14	chr15:77925532..77926425-chr15:78076783..78078398,4	MCF-7	breast:
15	chr15:78083797..78085667-chr15:78106019..78108853,2	K562	blood:
16	chr15:77925072..77927787-chr15:78111223..78115888,59	MCF-7	breast:
17	chr15:77925397..77928069-chr15:78112259..78116246,3	K562	blood:
18	chr15:77925397..77927315-chr15:78112259..78115116,2	K562	blood:
19	chr15:77411244..77411752-chr15:78113897..78114465,2	K562	blood:
20	chr15:78118529..78120395-chr15:78122461..78124625,2	K562	blood:
21	chr15:78125331..78127542-chr15:78130355..78132025,2	K562	blood:
22	chr15:78109668..78112280-chr15:78112604..78115106,3	MCF-7	breast:
23	chr15:78062199..78064857-chr15:78066773..78068430,2	K562	blood:
24	chr15:78109668..78112280-chr15:78112604..78115106,3	MCF-7	breast:
25	chr15:78088888..78092011-chr15:78092368..78096073,3	K562	blood:
26	chr15:77835732..77836546-chr15:78113747..78114395,2	MCF-7	breast:
27	chr15:78092486..78095378-chr15:78106571..78109428,2	K562	blood:
28	chr15:78097737..78099826-chr15:78103179..78105100,2	MCF-7	breast:
29	chr15:78093726..78095482-chr15:78109302..78111368,2	K562	blood:
30	chr15:78125331..78127542-chr15:78130355..78132025,2	K562	blood:
31	chr15:77951815..77952789-chr15:78075941..78076556,2	K562	blood:
32	chr15:77951738..77952728-chr15:78113529..78114461,5	K562	blood:
33	chr15:78116064..78118754-chr15:78122840..78125004,2	MCF-7	breast:
34	chr15:78116064..78118754-chr15:78122840..78125004,2	MCF-7	breast:
35	chr15:78041656..78043427-chr15:78100097..78102130,2	MCF-7	breast:
36	chr15:78066595..78068537-chr15:78076215..78077798,2	K562	blood:
37	chr15:78062199..78064857-chr15:78066773..78068430,2	K562	blood:
38	chr15:77923251..77928296-chr15:78111448..78115771,8	MCF-7	breast:
39	chr15:78079574..78081366-chr15:78081562..78083403,2	MCF-7	breast:
40	chr15:77925509..77926398-chr15:78076937..78077835,4	K562	blood:
41	chr15:78097465..78099114-chr15:78102921..78104806,2	K562	blood:
42	chr15:78092486..78095378-chr15:78106571..78109428,2	K562	blood:
43	chr15:78118529..78120395-chr15:78122461..78124625,2	K562	blood:
44	chr15:78059582..78063718-chr15:78064964..78067132,3	K562	blood:
45	chr15:77951785..77952749-chr15:78113535..78114168,4	MCF-7	breast:
46	chr15:77917906..77920772-chr15:78100061..78102458,2	K562	blood:
47	chr15:78066595..78068537-chr15:78076215..78077798,2	K562	blood:
48	chr15:78097737..78099826-chr15:78103179..78105100,2	MCF-7	breast:
49	chr15:78099210..78100960-chr15:78102155..78104684,2	K562	blood:
50	chr15:78064180..78065710-chr15:78076746..78078989,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH2D7-5	chr15:78080231-78080917	ENSG00000259213.1
2	lnc-SH2D7-5	chr15:78080231-78081011	XLOC_011317
3	lnc-TBC1D2B-7	chr15:78113121-78113196	NONHSAT047459
4	lnc-TBC1D2B-7	chr15:78112376-78112566	NONHSAT047460
5	lnc-SH2D7-5	chr15:78080414-78080487	ENSG00000259213.1
6	lnc-TBC1D2B-7	chr15:78088281-78088395	NONHSAT047460
7	lnc-SH2D7-5	chr15:78080723-78081016	ENSG00000259213.1
8	lnc-TBC1D2B-7	chr15:78088281-78088395	NONHSAT047459
9	lnc-TBC1D2B-7	chr15:78088281-78088395	NONHSAT047458
10	lnc-SH2D7-5	chr15:78079535-78079589	ENSG00000259213.1
11	lnc-SH2D7-5	chr15:78079529-78079589	XLOC_011317
12	lnc-TBC1D2B-7	chr15:78111613-78111870	NONHSAT047458

No data

Variant related genes	Relation type
ENSG00000259213	TF binding region
LINGO1	TF binding region
ENSG00000259213	CpG island
LINGO1	CpG island
ENSG00000259213	chromatin interactions
ENSG00000171940	chromatin interactions
ENSG00000169783	chromatin interactions
ENSG00000259281	chromatin interactions

Extended variants
information (count: 2686 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:2686 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8035460	chr15:78064664-78064665	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181589959	chr15:78064726-78064727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568332102	chr15:78064727-78064728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs145715812	chr15:78064736-78064737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554887495	chr15:78064783-78064784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148920727	chr15:78064799-78064800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569845809	chr15:78064804-78064805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143720332	chr15:78064805-78064806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537069646	chr15:78064823-78064824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185615665	chr15:78064846-78064847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558571797	chr15:78064883-78064884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577028939	chr15:78064884-78064885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541098351	chr15:78064893-78064894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs8035962	chr15:78064905-78064906	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs72730718	chr15:78064911-78064912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs148821111	chr15:78064927-78064928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542845018	chr15:78064930-78064931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561673115	chr15:78064938-78064939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374127296	chr15:78064965-78064966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114756627	chr15:78065007-78065008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146593292	chr15:78065030-78065031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs377606699	chr15:78065107-78065108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567187080	chr15:78065118-78065119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556460764	chr15:78065120-78065121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs543448433	chr15:78065126-78065127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564904694	chr15:78065129-78065130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112924749	chr15:78065182-78065183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370577734	chr15:78065216-78065217	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138416079	chr15:78065218-78065219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs12592419	chr15:78065224-78065225	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs529944829	chr15:78065248-78065249	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548056947	chr15:78065254-78065255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572997362	chr15:78065272-78065273	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs116069870	chr15:78065273-78065274	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558607821	chr15:78065306-78065307	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142413402	chr15:78065386-78065387	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534716869	chr15:78065404-78065405	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535173307	chr15:78065405-78065406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146847220	chr15:78065430-78065431	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574447196	chr15:78065457-78065458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs35194002	chr15:78065493-78065494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139239779	chr15:78065519-78065520	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74771580	chr15:78065551-78065552	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs554849438	chr15:78065566-78065567	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs555454716	chr15:78065570-78065571	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs373142311	chr15:78065627-78065628	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs565505815	chr15:78065658-78065659	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs372653606	chr15:78065665-78065666	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs117458607	chr15:78065743-78065744	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs189914717	chr15:78065762-78065763	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:780 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78061800-78074800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr15:78062200-78068000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:78064600-78068600	Weak transcription	Spleen	Spleen
4	chr15:78065200-78066600	Strong transcription	Fetal Intestine Small	intestine
5	chr15:78065800-78066200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr15:78066400-78068200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
7	chr15:78066600-78072600	Weak transcription	Fetal Intestine Small	intestine
8	chr15:78067200-78068000	Enhancers	Fetal Brain Female	brain
9	chr15:78067200-78068200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr15:78067400-78067600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr15:78067600-78068000	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr15:78067600-78068600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr15:78068000-78068800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr15:78068000-78073000	Weak transcription	Fetal Brain Female	brain
15	chr15:78068000-78076400	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr15:78068200-78068600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr15:78068200-78078200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr15:78068600-78068800	Enhancers	H1 Cell Line	embryonic stem cell
19	chr15:78068600-78068800	Enhancers	Fetal Muscle Trunk	muscle
20	chr15:78068600-78069000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr15:78068600-78069200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr15:78068600-78069200	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr15:78068600-78069200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr15:78068600-78069600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr15:78068600-78069600	Enhancers	Spleen	Spleen
26	chr15:78068600-78069800	Enhancers	Fetal Brain Male	brain
27	chr15:78068800-78069400	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr15:78069000-78069200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr15:78069000-78069400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr15:78069200-78069600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr15:78069200-78069600	Enhancers	Fetal Muscle Trunk	muscle
32	chr15:78069200-78072200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr15:78069400-78069600	Enhancers	H1 Cell Line	embryonic stem cell
34	chr15:78069600-78070400	Weak transcription	Spleen	Spleen
35	chr15:78069800-78072000	Weak transcription	Fetal Brain Male	brain
36	chr15:78070400-78070600	Enhancers	Spleen	Spleen
37	chr15:78070400-78071600	Weak transcription	Fetal Stomach	stomach
38	chr15:78070600-78072000	Weak transcription	Spleen	Spleen
39	chr15:78072000-78072800	ZNF genes & repeats	Spleen	Spleen
40	chr15:78072000-78077600	Enhancers	Fetal Brain Male	brain
41	chr15:78072200-78072400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr15:78072400-78072600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr15:78072400-78072800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr15:78072400-78078400	Weak transcription	Brain Angular Gyrus	brain
45	chr15:78072600-78073400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr15:78072600-78073400	ZNF genes & repeats	Fetal Intestine Small	intestine
47	chr15:78072800-78073000	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr15:78072800-78073600	ZNF genes & repeats	Brain Germinal Matrix	brain
49	chr15:78073000-78077600	Enhancers	Fetal Brain Female	brain
50	chr15:78073400-78074400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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