Variant report

Variant	esv1806493
Chromosome Location	chr15:78106177-78119345
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:529)
CpG islands
(count:977)
Chromatin interactive
region (count:25)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:529 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr15:78112581-78112794	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr15:78111596-78111934	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr15:78112561-78112947	K562	blood:	n/a	n/a
4	BHLHE40	chr15:78113211-78113483	K562	blood:	n/a	chr15:78113370-78113391 chr15:78113374-78113387
5	BHLHE40	chr15:78113815-78114121	K562	blood:	n/a	chr15:78113828-78113844
6	BRCA1	chr15:78116340-78116364	Hela-S3	cervix:	n/a	n/a
7	CCNT2	chr15:78112531-78112910	K562	blood:	n/a	n/a
8	CHD1	chr15:78111718-78111742	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr15:78112731-78112878	Hela-S3	cervix:	n/a	n/a
10	CHD2	chr15:78114017-78114116	K562	blood:	n/a	n/a
11	CHD2	chr15:78112768-78112882	H1-hESC	embryonic stem cell:	n/a	n/a
12	CREB1	chr15:78112210-78112963	A549	lung:	n/a	n/a
13	CTBP2	chr15:78111581-78112011	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr15:78113535-78114400	HCT-116	colon:	n/a	chr15:78113982-78114000
15	CTCF	chr15:78113100-78113250	GM06990	blood:	n/a	n/a
16	CTCF	chr15:78113783-78114184	GM12878	blood:	n/a	chr15:78113982-78114000
17	CTCF	chr15:78112840-78112990	GM12873	blood:	n/a	n/a
18	CTCF	chr15:78113841-78114143	NHEK	skin:	n/a	chr15:78113982-78114000
19	CTCF	chr15:78112699-78112843	GM10248	blood:	n/a	chr15:78112771-78112781
20	CTCF	chr15:78112740-78112890	GM12864	blood:	n/a	chr15:78112771-78112781
21	CTCF	chr15:78113920-78114070	HEEpiC	esophagus:	n/a	chr15:78113982-78114000
22	CTCF	chr15:78113754-78114152	K562	blood:	n/a	chr15:78113982-78114000
23	CTCF	chr15:78113900-78114050	GM12873	blood:	n/a	chr15:78113982-78114000
24	CTCF	chr15:78112680-78112930	GM12869	blood:	n/a	chr15:78112771-78112781
25	CTCF	chr15:78113880-78114030	GM12867	blood:	n/a	chr15:78113982-78114000
26	CTCF	chr15:78113900-78114050	HEK293	kidney:	n/a	chr15:78113982-78114000
27	CTCF	chr15:78112640-78112790	GM12864	blood:	n/a	chr15:78112771-78112781
28	CTCF	chr15:78112720-78112870	HepG2	liver:	n/a	chr15:78112771-78112781
29	CTCF	chr15:78113840-78113990	HAc	cerebellar:	n/a	n/a
30	CTCF	chr15:78113920-78114070	GM12875	blood:	n/a	chr15:78113982-78114000
31	CTCF	chr15:78113900-78114050	HUVEC	blood vessel:	n/a	chr15:78113982-78114000
32	CTCF	chr15:78112580-78112730	GM12865	blood:	n/a	chr15:78112615-78112628 chr15:78112615-78112624
33	CTCF	chr15:78113900-78114050	HRE	kidney:	n/a	chr15:78113982-78114000
34	CTCF	chr15:78112760-78112910	BJ	skin:	n/a	chr15:78112771-78112781
35	CTCF	chr15:78113920-78114070	GM12865	blood:	n/a	chr15:78113982-78114000
36	CTCF	chr15:78114104-78114105	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr15:78112720-78112870	SK-N-SH_RA	brain:	n/a	chr15:78112771-78112781
38	CTCF	chr15:78114760-78114910	GM12873	blood:	n/a	n/a
39	CTCF	chr15:78113920-78114070	NHEK	skin:	n/a	chr15:78113982-78114000
40	CTCF	chr15:78112685-78112875	GM19238	blood:	n/a	chr15:78112771-78112781
41	CTCF	chr15:78115800-78115950	HepG2	liver:	n/a	n/a
42	CTCF	chr15:78112511-78112987	K562	blood:	n/a	chr15:78112615-78112628 chr15:78112615-78112624 chr15:78112771-78112781
43	CTCF	chr15:78112680-78112830	A549	lung:	n/a	chr15:78112771-78112781
44	CTCF	chr15:78112693-78112845	LNCaP	prostate:	n/a	chr15:78112771-78112781
45	CTCF	chr15:78112660-78112810	NB4	blood:	n/a	chr15:78112771-78112781
46	CTCF	chr15:78112659-78112925	Gliobla	brain:	n/a	chr15:78112771-78112781
47	CTCF	chr15:78112578-78112897	K562	blood:	n/a	chr15:78112615-78112628 chr15:78112615-78112624 chr15:78112771-78112781
48	CTCF	chr15:78113920-78114070	AoAF	blood vessel:	n/a	chr15:78113982-78114000
49	CTCF	chr15:78112714-78112825	HUVEC	blood vessel:	n/a	chr15:78112771-78112781
50	CTCF	chr15:78112700-78112850	BE2_C	brain:	n/a	chr15:78112771-78112781

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:78112818-78112868	LNCaP	prostate:	n/a
2	chr15:78112818-78112868	LNCaP	prostate:	n/a
3	chr15:78112026-78112076	HCT-116	colon:	n/a
4	chr15:78110857-78110907	NB4	blood:	n/a
5	chr15:78113237-78113287	HMEC	breast:	n/a
6	chr15:78118816-78118866	HRE	kidney:	n/a
7	chr15:78112818-78112868	RPTEC	kidney:	n/a
8	chr15:78110903-78110953	HIPEpiC	eye:	n/a
9	chr15:78110857-78110907	HIPEpiC	eye:	n/a
10	chr15:78110903-78110953	HAEpiC	amniotic membrane:	n/a
11	chr15:78108562-78108612	HL-60	blood:	n/a
12	chr15:78112847-78112897	HRE	kidney:	n/a
13	chr15:78110903-78110953	GM12878	blood:	n/a
14	chr15:78112818-78112868	SK-N-SH_RA	brain:	n/a
15	chr15:78109450-78109500	GM06990	blood:	n/a
16	chr15:78112026-78112076	GM12891	blood:	n/a
17	chr15:78110106-78110156	HCPEpiC	choroid plexus:	n/a
18	chr15:78111390-78111440	SK-N-SH_RA	brain:	n/a
19	chr15:78111196-78111246	HNPCEpiC	eye:	n/a
20	chr15:78109450-78109500	NT2-D1	testis:	n/a
21	chr15:78111830-78111880	Hepatocyte	liver:	n/a
22	chr15:78110106-78110156	GM19239	blood:	n/a
23	chr15:78118816-78118866	BJ	skin:	n/a
24	chr15:78112026-78112076	HEEpiC	esophagus:	n/a
25	chr15:78113237-78113287	AoSMC	blood vessel:	n/a
26	chr15:78110857-78110907	SAEC	small airway:	n/a
27	chr15:78114278-78114328	NB4	blood:	n/a
28	chr15:78110106-78110156	NB4	blood:	n/a
29	chr15:78111830-78111880	AG04450	lung:	fetal
30	chr15:78108562-78108612	NB4	blood:	n/a
31	chr15:78113667-78113717	SK-N-MC	brain:	n/a
32	chr15:78114888-78114938	ovcar-3	ovarian:	n/a
33	chr15:78109450-78109500	AG09309	skin:	n/a
34	chr15:78113237-78113287	MCF-7	breast:	n/a
35	chr15:78112026-78112076	SK-N-MC	brain:	n/a
36	chr15:78111830-78111880	IMR90	lung:	fetal
37	chr15:78112818-78112868	NB4	blood:	n/a
38	chr15:78113237-78113287	AG04450	lung:	fetal
39	chr15:78108562-78108612	HMEC	breast:	n/a
40	chr15:78113667-78113717	GM12878	blood:	n/a
41	chr15:78118816-78118866	RPTEC	kidney:	n/a
42	chr15:78109450-78109500	HPAEpiC	pulmonary alveolar:	n/a
43	chr15:78114888-78114938	ProgFib	skin:	n/a
44	chr15:78112818-78112868	Caco-2	colon:	n/a
45	chr15:78112026-78112076	GM06990	blood:	n/a
46	chr15:78114278-78114328	T-47D	breast:	n/a
47	chr15:78110106-78110156	MCF-7	breast:	n/a
48	chr15:78111390-78111440	K562	blood:	n/a
49	chr15:78109450-78109500	GM12878	blood:	n/a
50	chr15:78112026-78112076	HCPEpiC	choroid plexus:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:77950482..77951067-chr15:78113646..78114389,2	K562	blood:
2	chr15:77835732..77836546-chr15:78113747..78114395,2	MCF-7	breast:
3	chr15:77925397..77927315-chr15:78112259..78115116,2	K562	blood:
4	chr15:78109668..78112280-chr15:78112604..78115106,3	MCF-7	breast:
5	chr15:77925299..77927652-chr15:78112444..78114100,3	MCF-7	breast:
6	chr15:78116064..78118754-chr15:78122840..78125004,2	MCF-7	breast:
7	chr15:78093726..78095482-chr15:78109302..78111368,2	K562	blood:
8	chr15:77951738..77952728-chr15:78113529..78114461,5	K562	blood:
9	chr15:78115470..78116424-chr15:78167241..78167877,2	MCF-7	breast:
10	chr15:78083797..78085667-chr15:78106019..78108853,2	K562	blood:
11	chr15:77925249..77927257-chr15:78113205..78115049,24	MCF-7	breast:
12	chr15:77411244..77411752-chr15:78113897..78114465,2	K562	blood:
13	chr15:77951840..77952665-chr15:78112887..78114250,4	MCF-7	breast:
14	chr15:78092486..78095378-chr15:78106571..78109428,2	K562	blood:
15	chr15:77925397..77928069-chr15:78112259..78116246,3	K562	blood:
16	chr15:78107758..78109313-chr15:78111361..78113671,2	K562	blood:
17	chr15:78103078..78104823-chr15:78106896..78108558,2	K562	blood:
18	chr15:77925435..77927439-chr15:78112259..78115090,22	K562	blood:
19	chr15:78109668..78112280-chr15:78112604..78115106,3	MCF-7	breast:
20	chr15:77925072..77927787-chr15:78111223..78115888,59	MCF-7	breast:
21	chr15:78118529..78120395-chr15:78122461..78124625,2	K562	blood:
22	chr15:77951785..77952749-chr15:78113535..78114168,4	MCF-7	breast:
23	chr15:77923251..77928296-chr15:78111448..78115771,8	MCF-7	breast:
24	chr15:77948459..77951097-chr15:78104975..78107913,2	MCF-7	breast:
25	chr15:78115466..78118484-chr15:78120011..78123409,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TBC1D2B-7	chr15:78111613-78111870	NONHSAT047458
2	lnc-TBC1D2B-7	chr15:78113121-78113196	NONHSAT047459
3	lnc-TBC1D2B-7	chr15:78112376-78112566	NONHSAT047460

No data

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

Extended variants
information (count: 513 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:513 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374349925	chr15:78106177-78106178	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs569562420	chr15:78106190-78106191	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs183827093	chr15:78106194-78106195	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs139853352	chr15:78106206-78106207	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs576495941	chr15:78106226-78106227	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs570083520	chr15:78106239-78106240	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs553974233	chr15:78106252-78106253	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs572589625	chr15:78106255-78106256	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs542959576	chr15:78106318-78106319	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs561581548	chr15:78106329-78106330	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs59403190	chr15:78106333-78106334	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs538999769	chr15:78106341-78106342	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs542750424	chr15:78106343-78106344	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs137888528	chr15:78106348-78106349	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs373855247	chr15:78106350-78106351	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs564388956	chr15:78106369-78106370	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs61326106	chr15:78106378-78106379	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs532678822	chr15:78106382-78106383	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs547907311	chr15:78106387-78106388	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs565779469	chr15:78106457-78106458	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs565953291	chr15:78106483-78106484	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529859708	chr15:78106534-78106535	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs548193595	chr15:78106548-78106549	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs554365583	chr15:78106610-78106611	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569907187	chr15:78106683-78106684	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs79362461	chr15:78106696-78106697	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558164881	chr15:78106697-78106698	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376254448	chr15:78106708-78106709	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs149306415	chr15:78106719-78106720	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534459572	chr15:78106778-78106779	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs546154095	chr15:78106848-78106849	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374512770	chr15:78106865-78106866	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144541819	chr15:78106875-78106876	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs367789055	chr15:78106916-78106917	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572554985	chr15:78106961-78106962	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs536827264	chr15:78106962-78106963	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534613135	chr15:78106974-78106975	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs554979544	chr15:78106978-78106979	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576705311	chr15:78106995-78106996	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188771460	chr15:78107047-78107048	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs116239209	chr15:78107049-78107050	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs577299971	chr15:78107067-78107068	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs541548872	chr15:78107081-78107082	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs559752790	chr15:78107105-78107106	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs529870185	chr15:78107117-78107118	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs548334976	chr15:78107118-78107119	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs554296539	chr15:78107161-78107162	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs530743630	chr15:78107162-78107163	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs4886919	chr15:78107164-78107165	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs570121452	chr15:78107265-78107266	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	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:393 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78100800-78106400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:78100800-78108400	Weak transcription	Fetal Brain Female	brain
3	chr15:78101000-78107200	Weak transcription	Brain Cingulate Gyrus	brain
4	chr15:78101400-78106400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr15:78101600-78110400	Weak transcription	Brain Angular Gyrus	brain
6	chr15:78102800-78108200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr15:78103600-78107200	Weak transcription	Gastric	stomach
8	chr15:78104800-78109200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr15:78104800-78109200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr15:78105600-78106400	Enhancers	Fetal Brain Male	brain
11	chr15:78105800-78109800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
12	chr15:78106000-78107000	Weak transcription	Placenta	Placenta
13	chr15:78106200-78106600	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr15:78106400-78108200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr15:78106400-78108200	Weak transcription	Fetal Brain Male	brain
16	chr15:78106400-78108400	Enhancers	Fetal Muscle Leg	muscle
17	chr15:78106400-78109200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr15:78107000-78107600	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr15:78107000-78107600	Enhancers	Placenta	Placenta
20	chr15:78107200-78107400	Enhancers	Gastric	stomach
21	chr15:78107200-78107600	Enhancers	Brain Cingulate Gyrus	brain
22	chr15:78107400-78107600	Enhancers	Esophagus	oesophagus
23	chr15:78107400-78107600	Bivalent Enhancer	Fetal Stomach	stomach
24	chr15:78107400-78111600	Weak transcription	Gastric	stomach
25	chr15:78107600-78109400	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr15:78108200-78108400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
27	chr15:78108200-78108800	Enhancers	Fetal Brain Male	brain
28	chr15:78108200-78109600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr15:78108400-78108600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr15:78108400-78108600	Enhancers	Fetal Brain Female	brain
31	chr15:78108400-78109000	Bivalent Enhancer	Fetal Muscle Leg	muscle
32	chr15:78108600-78108800	Bivalent Enhancer	Placenta	Placenta
33	chr15:78108800-78109800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr15:78108800-78110600	Bivalent Enhancer	Fetal Brain Male	brain
35	chr15:78109000-78110600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr15:78109000-78110800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr15:78109200-78109400	Bivalent/Poised TSS	Fetal Brain Female	brain
38	chr15:78109200-78109600	Bivalent Enhancer	Fetal Muscle Leg	muscle
39	chr15:78109200-78109800	Enhancers	H9 Cell Line	embryonic stem cell
40	chr15:78109200-78110200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr15:78109200-78110600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr15:78109200-78110600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
43	chr15:78109400-78109800	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr15:78109400-78110400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
45	chr15:78109400-78110400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr15:78109400-78110600	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
47	chr15:78109400-78110800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
48	chr15:78109600-78109800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr15:78109600-78109800	Bivalent Enhancer	Brain Cingulate Gyrus	brain
50	chr15:78109600-78109800	Active TSS	Spleen	Spleen

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