Variant report

Variant	nsv904427
Chromosome Location	chr15:78129964-78251431
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3314)
CpG islands
(count:1528)
Chromatin interactive
region (count:44)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3314 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:78235026-78235383	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:78236893-78236910	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:78162883-78163100	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:78237679-78237763	K562	blood:	n/a	n/a
5	ATF1	chr15:78151266-78151590	K562	blood:	n/a	n/a
6	ATF1	chr15:78219190-78219467	K562	blood:	n/a	n/a
7	ATF3	chr15:78236808-78236989	K562	blood:	n/a	n/a
8	ATF3	chr15:78246365-78246569	K562	blood:	n/a	n/a
9	BACH1	chr15:78191284-78191344	K562	blood:	n/a	n/a
10	BATF	chr15:78202770-78203254	GM12878	blood:	n/a	n/a
11	BATF	chr15:78240702-78240880	GM12878	blood:	n/a	n/a
12	BATF	chr15:78246140-78246599	GM12878	blood:	n/a	n/a
13	BATF	chr15:78246086-78246649	GM12878	blood:	n/a	n/a
14	BATF	chr15:78200510-78200771	GM12878	blood:	n/a	n/a
15	BCL11A	chr15:78246175-78246575	GM12878	blood:	n/a	n/a
16	BCL11A	chr15:78236927-78237145	GM12878	blood:	n/a	n/a
17	BCL11A	chr15:78246237-78246453	GM12878	blood:	n/a	n/a
18	BCL11A	chr15:78202965-78203220	GM12878	blood:	n/a	chr15:78202981-78202994
19	BCL11A	chr15:78181243-78181441	GM12878	blood:	n/a	chr15:78181308-78181321
20	BCL11A	chr15:78183650-78183946	GM12878	blood:	n/a	n/a
21	BCL3	chr15:78177816-78178379	GM12878	blood:	n/a	n/a
22	BCL3	chr15:78177167-78177695	GM12878	blood:	n/a	chr15:78177500-78177509 chr15:78177265-78177274
23	BCL3	chr15:78177756-78178421	GM12878	blood:	n/a	n/a
24	BCL3	chr15:78177235-78177691	GM12878	blood:	n/a	chr15:78177500-78177509 chr15:78177265-78177274
25	BCL3	chr15:78191128-78191516	GM12878	blood:	n/a	n/a
26	BCL3	chr15:78191134-78191391	GM12878	blood:	n/a	n/a
27	BHLHE40	chr15:78167567-78167705	GM12878	blood:	n/a	n/a
28	BHLHE40	chr15:78162833-78163083	K562	blood:	n/a	n/a
29	BHLHE40	chr15:78200229-78200546	K562	blood:	n/a	n/a
30	BHLHE40	chr15:78176969-78177063	K562	blood:	n/a	n/a
31	BHLHE40	chr15:78236789-78237064	GM12878	blood:	n/a	n/a
32	BHLHE40	chr15:78143515-78143667	K562	blood:	n/a	n/a
33	BHLHE40	chr15:78192717-78192924	K562	blood:	n/a	n/a
34	BHLHE40	chr15:78151239-78151677	K562	blood:	n/a	n/a
35	BHLHE40	chr15:78236781-78237088	HepG2	liver:	n/a	n/a
36	BHLHE40	chr15:78202964-78203186	K562	blood:	n/a	n/a
37	BHLHE40	chr15:78151267-78151451	GM12878	blood:	n/a	n/a
38	BHLHE40	chr15:78162937-78162982	GM12878	blood:	n/a	n/a
39	BHLHE40	chr15:78236789-78237097	K562	blood:	n/a	n/a
40	BHLHE40	chr15:78181314-78181673	GM12878	blood:	n/a	n/a
41	BHLHE40	chr15:78183229-78183978	GM12878	blood:	n/a	n/a
42	BHLHE40	chr15:78190603-78190942	K562	blood:	n/a	chr15:78190757-78190766 chr15:78190757-78190766 chr15:78190758-78190767
43	BHLHE40	chr15:78195387-78195410	GM12878	blood:	n/a	n/a
44	BHLHE40	chr15:78137185-78137422	GM12878	blood:	n/a	n/a
45	BHLHE40	chr15:78197822-78197825	K562	blood:	n/a	n/a
46	BHLHE40	chr15:78203005-78203198	GM12878	blood:	n/a	n/a
47	BHLHE40	chr15:78200363-78200447	GM12878	blood:	n/a	n/a
48	BHLHE40	chr15:78177249-78177916	GM12878	blood:	n/a	n/a
49	BHLHE40	chr15:78191369-78191376	K562	blood:	n/a	n/a
50	BHLHE40	chr15:78156549-78156840	K562	blood:	n/a	n/a

(count:1528 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:78133639-78133689	ProgFib	skin:	n/a
2	chr15:78196287-78196337	HEEpiC	esophagus:	n/a
3	chr15:78219273-78219323	AG10803	skin:	n/a
4	chr15:78133639-78133689	ProgFib	skin:	n/a
5	chr15:78196287-78196337	HEEpiC	esophagus:	n/a
6	chr15:78219273-78219323	AG10803	skin:	n/a
7	chr15:78133639-78133689	RPTEC	kidney:	n/a
8	chr15:78200484-78200534	AG10803	skin:	n/a
9	chr15:78189695-78189745	HEEpiC	esophagus:	n/a
10	chr15:78219748-78219798	PrEC	prostate:	n/a
11	chr15:78191179-78191229	SK-N-SH	brain:	n/a
12	chr15:78219748-78219798	BE2_C	brain:	n/a
13	chr15:78189752-78189802	NB4	blood:	n/a
14	chr15:78236860-78236910	ovcar-3	ovarian:	n/a
15	chr15:78237003-78237053	CMK	blood:	n/a
16	chr15:78237003-78237053	ovcar-3	ovarian:	n/a
17	chr15:78189625-78189675	ProgFib	skin:	n/a
18	chr15:78196623-78196673	ovcar-3	ovarian:	n/a
19	chr15:78236707-78236757	SAEC	small airway:	n/a
20	chr15:78208251-78208301	T-47D	breast:	n/a
21	chr15:78233786-78233836	AG04450	lung:	fetal
22	chr15:78237003-78237053	LNCaP	prostate:	n/a
23	chr15:78196623-78196673	HIPEpiC	eye:	n/a
24	chr15:78191179-78191229	NT2-D1	testis:	n/a
25	chr15:78189625-78189675	SK-N-MC	brain:	n/a
26	chr15:78186622-78186672	Hela-S3	cervix:	n/a
27	chr15:78237003-78237053	PANC-1	pancreas:	n/a
28	chr15:78240223-78240273	T-47D	breast:	n/a
29	chr15:78189695-78189745	GM19239	blood:	n/a
30	chr15:78238416-78238466	HCT-116	colon:	n/a
31	chr15:78236860-78236910	U87	brain:	n/a
32	chr15:78233786-78233836	CMK	blood:	n/a
33	chr15:78219423-78219473	NHDF-neo	bronchial:	n/a
34	chr15:78196623-78196673	HUVEC	blood vessel:	n/a
35	chr15:78189695-78189745	SK-N-SH	brain:	n/a
36	chr15:78219423-78219473	SKMC	muscle:	n/a
37	chr15:78233786-78233836	HPAEpiC	pulmonary alveolar:	n/a
38	chr15:78237003-78237053	HNPCEpiC	eye:	n/a
39	chr15:78196623-78196673	Caco-2	colon:	n/a
40	chr15:78219273-78219323	SK-N-SH	brain:	n/a
41	chr15:78240223-78240273	GM12892	blood:	n/a
42	chr15:78190123-78190173	HRE	kidney:	n/a
43	chr15:78236707-78236757	HEEpiC	esophagus:	n/a
44	chr15:78208251-78208301	HNPCEpiC	eye:	n/a
45	chr15:78186622-78186672	NHBE	bronchial:	n/a
46	chr15:78240223-78240273	HPAEpiC	pulmonary alveolar:	n/a
47	chr15:78240223-78240273	CMK	blood:	n/a
48	chr15:78191302-78191352	ovcar-3	ovarian:	n/a
49	chr15:78209119-78209169	HMEC	breast:	n/a
50	chr15:78237003-78237053	SAEC	small airway:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:78232364..78235120-chr15:78235300..78238762,3	K562	blood:
2	chr15:78145789..78149716-chr15:78150304..78153392,4	K562	blood:
3	chr15:78115470..78116424-chr15:78167241..78167877,2	MCF-7	breast:
4	chr15:78129825..78131680-chr15:78135529..78137556,2	K562	blood:
5	chr15:78170552..78173513-chr15:78177098..78179231,2	K562	blood:
6	chr15:78151615..78153202-chr15:78155593..78157169,2	MCF-7	breast:
7	chr15:78145789..78147609-chr15:78150785..78152558,2	K562	blood:
8	chr15:78200418..78201162-chr15:78910453..78911204,2	K562	blood:
9	chr15:78151280..78153244-chr15:78194302..78196153,2	MCF-7	breast:
10	chr15:78145789..78147609-chr15:78150785..78152558,2	K562	blood:
11	chr15:78125331..78127542-chr15:78130355..78132025,2	K562	blood:
12	chr15:78146921..78148792-chr15:78155697..78158259,2	K562	blood:
13	chr15:78146921..78148792-chr15:78155697..78158259,2	K562	blood:
14	chr15:77925519..77926294-chr15:78162494..78163468,3	MCF-7	breast:
15	chr15:78133236..78134995-chr15:78137476..78140280,2	K562	blood:
16	chr15:78133236..78134995-chr15:78137476..78140280,2	K562	blood:
17	chr15:77835482..77836422-chr15:78167231..78168063,2	K562	blood:
18	chr15:78236783..78237478-chrX:151999319..151999901,2	NB4	blood:
19	chr15:77925583..77927500-chr15:78167130..78168054,7	MCF-7	breast:
20	chr15:78251353..78252448-chr15:78400281..78401311,8	MCF-7	breast:
21	chr15:78170552..78173513-chr15:78177098..78179231,2	K562	blood:
22	chr15:78148872..78151118-chr15:78152940..78154458,3	MCF-7	breast:
23	chr15:77925526..77926907-chr15:78167143..78168054,6	MCF-7	breast:
24	chr15:77942627..77943302-chr15:78167255..78168112,2	MCF-7	breast:
25	chr15:78143411..78145783-chr15:78149960..78151669,2	MCF-7	breast:
26	chr15:78151280..78153244-chr15:78194302..78196153,2	MCF-7	breast:
27	chr15:78143411..78145783-chr15:78149960..78151669,2	MCF-7	breast:
28	chr15:77951644..77952520-chr15:78167212..78167992,3	MCF-7	breast:
29	chr15:75975803..75976315-chr15:78195454..78196010,2	K562	blood:
30	chr15:78162688..78164962-chr15:78166571..78168544,2	K562	blood:
31	chr15:77925576..77926405-chr15:78167119..78167924,3	K562	blood:
32	chr15:78148872..78151118-chr15:78152940..78154458,3	MCF-7	breast:
33	chr15:78251411..78252367-chr15:78280153..78280696,2	MCF-7	breast:
34	chr15:75978451..75979139-chr15:78192424..78193254,5	MCF-7	breast:
35	chr15:75978476..75979174-chr15:78192448..78193224,3	MCF-7	breast:
36	chr15:78200661..78201180-chr15:79032859..79033389,2	MCF-7	breast:
37	chr15:78162688..78164962-chr15:78166571..78168544,2	K562	blood:
38	chr15:78194874..78195656-chr15:78400670..78401266,2	MCF-7	breast:
39	chr15:78129825..78131680-chr15:78135529..78137556,2	K562	blood:
40	chr15:78251300..78252464-chr15:78292151..78292856,3	MCF-7	breast:
41	chr15:78151615..78153202-chr15:78155593..78157169,2	MCF-7	breast:
42	chr15:77925580..77926309-chr15:78156358..78157211,2	MCF-7	breast:
43	chr15:78145789..78149716-chr15:78150304..78153392,4	K562	blood:
44	chr15:78232364..78235120-chr15:78235300..78238762,3	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH2D7-9	chr15:78146122-78146242	NONHSAT047464
2	lnc-SH2D7-4	chr15:78208864-78208974	ENSG00000261244.1
3	lnc-TBC1D2B-1	chr15:78246417-78246686	ENSG00000261403.1
4	lnc-TBC1D2B-5	chr15:78209065-78209324	NONHSAT047472
5	lnc-SH2D7-4	chr15:78214120-78214361	ENSG00000261244.1
6	lnc-SH2D7-9	chr15:78145098-78145465	NONHSAT047464

No data

Variant related genes	Relation type
CSPG4P13	TF binding region
ENSG00000261244	TF binding region
RN7SL214P	TF binding region
ENSG00000260776	TF binding region
ENSG00000214646	TF binding region
CSPG4P13	CpG island
ENSG00000261244	CpG island
RN7SL214P	CpG island
ENSG00000260776	CpG island
ENSG00000214646	CpG island
ENSG00000169783	chromatin interactions
ENSG00000261143	chromatin interactions
ENSG00000147400	chromatin interactions
ENSG00000214646	chromatin interactions
ENSG00000147383	chromatin interactions
ENSG00000259281	chromatin interactions

Extended variants
information (count: 5835 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:5835 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7174757	chr15:78129964-78129965	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556882963	chr15:78130003-78130004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190230766	chr15:78130016-78130017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs56061318	chr15:78130088-78130089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535675012	chr15:78130098-78130099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569128608	chr15:78130109-78130110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539671210	chr15:78130154-78130155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs35487286	chr15:78130155-78130156	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs150157403	chr15:78130156-78130157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138233566	chr15:78130166-78130167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376745545	chr15:78130203-78130204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555744956	chr15:78130229-78130230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573918120	chr15:78130240-78130241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs371028441	chr15:78130307-78130308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112066539	chr15:78130320-78130321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533450396	chr15:78130322-78130323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181387451	chr15:78130342-78130343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs74026876	chr15:78130370-78130371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527586823	chr15:78130412-78130413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548965740	chr15:78130413-78130414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs74026878	chr15:78130433-78130434	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs531178102	chr15:78130440-78130441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs34628865	chr15:78130441-78130442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs549726204	chr15:78130503-78130504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs114235175	chr15:78130505-78130506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs538345320	chr15:78130513-78130514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs557935718	chr15:78130535-78130536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs11072680	chr15:78130580-78130581	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs373396866	chr15:78130595-78130596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs541600065	chr15:78130696-78130697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534523024	chr15:78130723-78130724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs555757777	chr15:78130729-78130730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs561471554	chr15:78130738-78130739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs574253810	chr15:78130747-78130748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs377145211	chr15:78130774-78130775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs377509407	chr15:78130776-78130777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs544316541	chr15:78130786-78130787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs556587556	chr15:78130803-78130804	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs578177690	chr15:78130811-78130812	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs545470629	chr15:78130819-78130820	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs560398636	chr15:78130842-78130843	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs369441370	chr15:78130914-78130915	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs8040443	chr15:78130915-78130916	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs561052792	chr15:78130961-78130962	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs531615453	chr15:78130979-78130980	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs549413996	chr15:78131005-78131006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142789982	chr15:78131036-78131037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532089136	chr15:78131077-78131078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547058592	chr15:78131078-78131079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs4886932	chr15:78131097-78131098	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:53)

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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1415 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78124800-78132800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr15:78125800-78132600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:78126200-78130600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr15:78128800-78133200	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr15:78129200-78132600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr15:78129200-78132600	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr15:78130400-78130800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr15:78130600-78131000	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr15:78130800-78131000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr15:78131800-78134200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr15:78132400-78132800	Bivalent Enhancer	Fetal Intestine Large	intestine
12	chr15:78132400-78133400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr15:78132400-78134200	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr15:78132400-78134800	Enhancers	Fetal Intestine Small	intestine
15	chr15:78132600-78133000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr15:78132600-78133200	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr15:78132600-78133600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr15:78132600-78134000	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr15:78132600-78134000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr15:78132600-78134200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr15:78132800-78133400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr15:78132800-78133600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr15:78132800-78134600	Enhancers	Fetal Intestine Large	intestine
24	chr15:78133000-78133200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr15:78133000-78133400	Bivalent Enhancer	NHEK	skin
26	chr15:78133000-78133600	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr15:78133000-78134200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr15:78133200-78133400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr15:78133200-78133600	Enhancers	H9 Cell Line	embryonic stem cell
30	chr15:78133200-78134000	Enhancers	H1 Cell Line	embryonic stem cell
31	chr15:78133200-78134000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr15:78133200-78134000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr15:78133200-78134000	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr15:78133200-78134000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr15:78133200-78134200	Bivalent Enhancer	A549	lung
36	chr15:78133200-78134200	Flanking Active TSS	Hela-S3	cervix
37	chr15:78133200-78134200	Enhancers	HMEC	breast
38	chr15:78133200-78134200	Bivalent Enhancer	Osteobl	bone
39	chr15:78133200-78134400	Enhancers	NH-A	brain
40	chr15:78133200-78134600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr15:78133200-78134600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr15:78133400-78133600	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr15:78133400-78134000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
44	chr15:78133400-78134200	Enhancers	NHEK	skin
45	chr15:78133600-78133800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
46	chr15:78133600-78133800	Bivalent Enhancer	HSMM	muscle
47	chr15:78133600-78134000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr15:78133600-78134200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr15:78133800-78134000	Bivalent Enhancer	Placenta	Placenta
50	chr15:78133800-78134200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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