Variant report

Variant	nsv1042033
Chromosome Location	chr14:24474511-24500989
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:558)
CpG islands
(count:366)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:558 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:24483175-24483522	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:24483172-24483507	K562	blood:	n/a	n/a
3	BACH1	chr14:24476252-24476312	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr14:24483187-24483465	GM12878	blood:	n/a	n/a
5	BHLHE40	chr14:24483227-24483438	K562	blood:	n/a	n/a
6	BHLHE40	chr14:24475943-24476541	HepG2	liver:	n/a	n/a
7	BRCA1	chr14:24483351-24483423	GM12878	blood:	n/a	n/a
8	CBX3	chr14:24483227-24483553	K562	blood:	n/a	n/a
9	CBX3	chr14:24483218-24483539	K562	blood:	n/a	n/a
10	CBX3	chr14:24476155-24476416	K562	blood:	n/a	n/a
11	CEBPB	chr14:24482978-24483461	A549	lung:	n/a	n/a
12	CEBPD	chr14:24475992-24476248	HepG2	liver:	n/a	n/a
13	CHD1	chr14:24483316-24483498	GM12878	blood:	n/a	n/a
14	CHD2	chr14:24483281-24483447	GM12878	blood:	n/a	n/a
15	CTCF	chr14:24483280-24483430	SK-N-SH_RA	brain:	n/a	n/a
16	CTCF	chr14:24483260-24483410	HL-60	blood:	n/a	n/a
17	CTCF	chr14:24483220-24483370	GM12869	blood:	n/a	n/a
18	CTCF	chr14:24483280-24483430	GM12872	blood:	n/a	n/a
19	CTCF	chr14:24483260-24483410	HRE	kidney:	n/a	n/a
20	CTCF	chr14:24489140-24489290	GM12870	blood:	n/a	n/a
21	CTCF	chr14:24483073-24483654	HepG2	liver:	n/a	n/a
22	CTCF	chr14:24483195-24483455	GM10266	blood:	n/a	n/a
23	CTCF	chr14:24483179-24483476	Medullo	brain:	n/a	n/a
24	CTCF	chr14:24483147-24483522	ECC-1	luminal epithelium:	n/a	n/a
25	CTCF	chr14:24476148-24476235	Spleen_OC	spleen:	n/a	chr14:24476168-24476181
26	CTCF	chr14:24489404-24489445	HUVEC	blood vessel:	n/a	n/a
27	CTCF	chr14:24483220-24483370	HA-sp	spinal cord:	n/a	n/a
28	CTCF	chr14:24483162-24483512	K562	blood:	n/a	n/a
29	CTCF	chr14:24483280-24483430	HCM	heart:	n/a	n/a
30	CTCF	chr14:24483220-24483370	GM12878	blood:	n/a	n/a
31	CTCF	chr14:24489400-24489550	GM12871	blood:	n/a	n/a
32	CTCF	chr14:24489360-24489510	GM12874	blood:	n/a	n/a
33	CTCF	chr14:24483240-24483390	NHLF	lung:	n/a	n/a
34	CTCF	chr14:24483260-24483410	GM12868	blood:	n/a	n/a
35	CTCF	chr14:24483240-24483390	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr14:24489280-24489430	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr14:24483192-24483458	Pancreas_OC	pancreas:	n/a	n/a
38	CTCF	chr14:24489290-24489446	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr14:24489315-24489451	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr14:24489340-24489490	AG04449	skin:	n/a	n/a
41	CTCF	chr14:24489380-24489530	GM12868	blood:	n/a	n/a
42	CTCF	chr14:24482840-24482990	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr14:24482940-24483090	GM12878	blood:	n/a	n/a
44	CTCF	chr14:24483120-24483569	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr14:24489400-24489550	BE2_C	brain:	n/a	n/a
46	CTCF	chr14:24483199-24483448	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr14:24489302-24489433	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr14:24482840-24482990	AG10803	skin:	n/a	n/a
49	CTCF	chr14:24483260-24483410	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr14:24483180-24483330	WI-38	lung:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24475053-24475103	HCM	heart:	n/a
2	chr14:24475906-24475956	ECC-1	luminal epithelium:	n/a
3	chr14:24476559-24476609	NHDF-neo	bronchial:	n/a
4	chr14:24475906-24475956	H1-hESC	embryonic stem cell:	embryo
5	chr14:24476082-24476132	AG10803	skin:	n/a
6	chr14:24476082-24476132	SK-N-SH	brain:	n/a
7	chr14:24476082-24476132	HUVEC	blood vessel:	n/a
8	chr14:24475906-24475956	AG09309	skin:	n/a
9	chr14:24475053-24475103	GM12878	blood:	n/a
10	chr14:24475906-24475956	HCT-116	colon:	n/a
11	chr14:24475906-24475956	SK-N-SH_RA	brain:	n/a
12	chr14:24476559-24476609	SAEC	small airway:	n/a
13	chr14:24478620-24478670	CMK	blood:	n/a
14	chr14:24475053-24475103	RPTEC	kidney:	n/a
15	chr14:24476478-24476528	NH-A	brain:	n/a
16	chr14:24475053-24475103	PANC-1	pancreas:	n/a
17	chr14:24476559-24476609	SK-N-SH_RA	brain:	n/a
18	chr14:24476082-24476132	NHDF-neo	bronchial:	n/a
19	chr14:24476478-24476528	PANC-1	pancreas:	n/a
20	chr14:24476082-24476132	HPAEpiC	pulmonary alveolar:	n/a
21	chr14:24475053-24475103	A549	lung:	n/a
22	chr14:24476559-24476609	AoSMC	blood vessel:	n/a
23	chr14:24476559-24476609	AG10803	skin:	n/a
24	chr14:24478620-24478670	AG04449	skin:	fetal
25	chr14:24475053-24475103	MCF-7	breast:	n/a
26	chr14:24476478-24476528	SK-N-SH	brain:	n/a
27	chr14:24475053-24475103	Hela-S3	cervix:	n/a
28	chr14:24476082-24476132	H1-hESC	embryonic stem cell:	embryo
29	chr14:24476559-24476609	SK-N-SH	brain:	n/a
30	chr14:24478620-24478670	T-47D	breast:	n/a
31	chr14:24476559-24476609	ovcar-3	ovarian:	n/a
32	chr14:24476559-24476609	GM12878	blood:	n/a
33	chr14:24478620-24478670	Caco-2	colon:	n/a
34	chr14:24476082-24476132	MCF-7	breast:	n/a
35	chr14:24475053-24475103	PFSK-1	brain:	n/a
36	chr14:24478620-24478670	NHDF-neo	bronchial:	n/a
37	chr14:24475053-24475103	GM12892	blood:	n/a
38	chr14:24476478-24476528	MCF-7	breast:	n/a
39	chr14:24475906-24475956	Jurkat	blood:	n/a
40	chr14:24475906-24475956	HRCEpiC	kidney:	n/a
41	chr14:24478620-24478670	HPAEpiC	pulmonary alveolar:	n/a
42	chr14:24475906-24475956	HRE	kidney:	n/a
43	chr14:24476478-24476528	GM19239	blood:	n/a
44	chr14:24475906-24475956	AG04450	lung:	fetal
45	chr14:24476082-24476132	BJ	skin:	n/a
46	chr14:24476478-24476528	GM06990	blood:	n/a
47	chr14:24475906-24475956	MCF10A-Er-Src	breast:	n/a
48	chr14:24475053-24475103	Hepatocyte	liver:	n/a
49	chr14:24476559-24476609	GM19239	blood:	n/a
50	chr14:24475906-24475956	HCF	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:24482659..24484974-chr14:24503307..24504865,2	MCF-7	breast:
2	chr14:24476695..24479385-chr14:24563251..24564763,2	MCF-7	breast:
3	chr14:24482858..24483785-chr14:24559502..24560237,2	K562	blood:
4	chr14:24482802..24483800-chr14:24505642..24506553,4	MCF-7	breast:
5	chr14:24421533..24423333-chr14:24480435..24482151,2	K562	blood:
6	chr14:24482946..24483934-chr14:24503845..24504435,3	MCF-7	breast:
7	chr14:24482840..24483718-chr14:24710880..24711620,2	MCF-7	breast:
8	chr14:24483165..24483827-chr14:24559565..24560642,4	MCF-7	breast:
9	chr14:24483262..24483795-chr14:24906005..24906586,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000225766	TF binding region
ENSG00000225766	CpG island
ENSG00000225766	chromatin interactions
ENSG00000215256	chromatin interactions
ENSG00000129535	chromatin interactions
ENSG00000157326	chromatin interactions
ENSG00000100889	chromatin interactions
ENSG00000092330	chromatin interactions

Extended variants
information (count: 1095 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1095 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201034726	chr14:24474638-24474639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs530797127	chr14:24474687-24474688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs1062729	chr14:24474711-24474712	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs567625777	chr14:24474730-24474731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs536753782	chr14:24474790-24474791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546838768	chr14:24474813-24474814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567045841	chr14:24474841-24474842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs538912054	chr14:24474941-24474942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs376044607	chr14:24474942-24474943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs184702556	chr14:24474976-24474977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372778956	chr14:24474980-24474981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs386775664	chr14:24474989-24474990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs559920637	chr14:24475011-24475012	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530202251	chr14:24475027-24475028	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576042319	chr14:24475042-24475043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537809342	chr14:24475052-24475053	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554628689	chr14:24475053-24475054	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574404959	chr14:24475062-24475063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540334602	chr14:24475068-24475069	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560033187	chr14:24475076-24475077	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186823944	chr14:24475082-24475083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545625424	chr14:24475084-24475085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562407035	chr14:24475094-24475095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531521864	chr14:24475116-24475117	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2760086	chr14:24475177-24475178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550513955	chr14:24475179-24475180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561342827	chr14:24475190-24475191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs199548804	chr14:24475250-24475251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs146813679	chr14:24475259-24475260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1043501	chr14:24475265-24475266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547068366	chr14:24475273-24475274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372881743	chr14:24475292-24475293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566881017	chr14:24475293-24475294	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201582507	chr14:24475318-24475319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552821685	chr14:24475330-24475331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191202223	chr14:24475371-24475372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs369542947	chr14:24475375-24475376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373899901	chr14:24475386-24475387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554230423	chr14:24475475-24475476	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs202236552	chr14:24475489-24475490	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs55703791	chr14:24475495-24475496	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs574368858	chr14:24475548-24475549	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs533579312	chr14:24475553-24475554	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs200449993	chr14:24475564-24475565	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs576879450	chr14:24475615-24475616	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545564007	chr14:24475619-24475620	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201092772	chr14:24475674-24475675	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112825580	chr14:24475822-24475823	Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562345155	chr14:24475872-24475873	Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575891314	chr14:24475873-24475874	Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Cancer	20164920	CNVD
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21390271	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:413 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24458800-24476000	Weak transcription	Fetal Intestine Small	intestine
2	chr14:24459000-24475200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr14:24459200-24476000	Weak transcription	Liver	Liver
4	chr14:24459400-24475800	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr14:24459600-24474800	Weak transcription	Dnd41	blood
6	chr14:24470800-24475000	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr14:24471200-24475000	Weak transcription	Primary B cells from peripheral blood	blood
8	chr14:24471200-24475000	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr14:24472800-24476000	Weak transcription	Pancreas	Pancrea
10	chr14:24474000-24475800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr14:24474800-24475000	Enhancers	Primary B cells from cord blood	blood
12	chr14:24474800-24475000	Enhancers	Fetal Brain Female	brain
13	chr14:24474800-24475200	Enhancers	Primary T helper naive cells from peripheral blood	blood
14	chr14:24474800-24475400	Enhancers	Dnd41	blood
15	chr14:24475000-24475200	Enhancers	H1 Cell Line	embryonic stem cell
16	chr14:24475000-24475200	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr14:24475000-24475200	Enhancers	Brain Hippocampus Middle	brain
18	chr14:24475000-24475200	Enhancers	GM12878-XiMat	blood
19	chr14:24475000-24475200	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr14:24475000-24475800	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr14:24475000-24475800	Enhancers	Primary B cells from peripheral blood	blood
22	chr14:24475000-24475800	Enhancers	Primary T cells fromperipheralblood	blood
23	chr14:24475000-24475800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
24	chr14:24475000-24475800	Enhancers	Primary T helper cells PMA-I stimulated	--
25	chr14:24475000-24475800	Enhancers	Primary T helper cells fromperipheralblood	blood
26	chr14:24475000-24475800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr14:24475000-24475800	Enhancers	Fetal Muscle Leg	muscle
28	chr14:24475000-24475800	Enhancers	Stomach Smooth Muscle	stomach
29	chr14:24475000-24476000	Weak transcription	Primary B cells from cord blood	blood
30	chr14:24475200-24475600	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr14:24475200-24475800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr14:24475200-24475800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr14:24475200-24480000	Weak transcription	GM12878-XiMat	blood
34	chr14:24475400-24475600	Enhancers	Fetal Brain Male	brain
35	chr14:24475400-24475600	Flanking Active TSS	Dnd41	blood
36	chr14:24475400-24475800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr14:24475400-24475800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
38	chr14:24475400-24475800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr14:24475400-24475800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr14:24475400-24475800	Enhancers	Adipose Nuclei	Adipose
41	chr14:24475400-24475800	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr14:24475400-24475800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
43	chr14:24475400-24475800	Enhancers	Duodenum Mucosa	Duodenum
44	chr14:24475400-24475800	Enhancers	Placenta	Placenta
45	chr14:24475400-24475800	Enhancers	Skeletal Muscle Male	skeletal muscle
46	chr14:24475400-24475800	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr14:24475400-24475800	Enhancers	HepG2	liver
48	chr14:24475400-24476200	Active TSS	iPS-20b Cell Line	embryonic stem cell
49	chr14:24475400-24476600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr14:24475400-24476800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood

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