Variant report

Variant	nsv599062
Chromosome Location	chr5:97258619-97430527
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr5:97386385-97386732	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr5:97405650-97405889	GM12878	blood:	n/a	chr5:97405750-97405760 chr5:97405746-97405756
3	BCL11A	chr5:97378749-97378960	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr5:97259838-97260091	GM12878	blood:	n/a	n/a
5	CEBPB	chr5:97398022-97398187	A549	lung:	n/a	chr5:97398105-97398116
6	CEBPB	chr5:97397978-97398244	IMR90	lung:	n/a	chr5:97398105-97398116
7	CEBPB	chr5:97403339-97403632	IMR90	lung:	n/a	chr5:97403516-97403527
8	CEBPB	chr5:97403339-97403649	HepG2	liver:	n/a	chr5:97403516-97403527
9	CEBPB	chr5:97386400-97386600	K562	blood:	n/a	chr5:97386563-97386574
10	CEBPB	chr5:97386421-97386690	HepG2	liver:	n/a	chr5:97386563-97386574
11	CEBPB	chr5:97386386-97386756	Hela-S3	cervix:	n/a	chr5:97386563-97386574
12	CEBPB	chr5:97394376-97394700	HepG2	liver:	n/a	chr5:97394544-97394557 chr5:97394544-97394555
13	CEBPB	chr5:97386405-97386694	MCF-7	breast:	n/a	chr5:97386563-97386574
14	CEBPB	chr5:97397977-97398256	HepG2	liver:	n/a	chr5:97398105-97398116
15	CEBPB	chr5:97386430-97386669	A549	lung:	n/a	chr5:97386563-97386574
16	CEBPB	chr5:97288323-97288547	HepG2	liver:	n/a	chr5:97288387-97288400 chr5:97288387-97288400 chr5:97288519-97288532
17	CEBPB	chr5:97414072-97414411	HepG2	liver:	n/a	chr5:97414272-97414285 chr5:97414232-97414243
18	CEBPB	chr5:97414103-97414348	A549	lung:	n/a	chr5:97414272-97414285 chr5:97414232-97414243
19	CEBPB	chr5:97315569-97315781	IMR90	lung:	n/a	n/a
20	CEBPB	chr5:97324575-97324602	A549	lung:	n/a	n/a
21	CEBPB	chr5:97325294-97325607	IMR90	lung:	n/a	n/a
22	CEBPB	chr5:97324370-97324626	HepG2	liver:	n/a	chr5:97324472-97324483
23	CEBPB	chr5:97378783-97379050	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr5:97386366-97386723	IMR90	lung:	n/a	chr5:97386563-97386574
25	CEBPB	chr5:97324361-97324490	H1-hESC	embryonic stem cell:	n/a	chr5:97324472-97324483
26	CEBPB	chr5:97394381-97394670	A549	lung:	n/a	chr5:97394544-97394557 chr5:97394544-97394555
27	CEBPB	chr5:97385404-97385851	HepG2	liver:	n/a	chr5:97385748-97385759 chr5:97385748-97385761 chr5:97385748-97385759
28	CEBPB	chr5:97335052-97335326	HepG2	liver:	n/a	chr5:97335304-97335315 chr5:97335304-97335313
29	CEBPB	chr5:97403393-97403603	A549	lung:	n/a	chr5:97403516-97403527
30	CHD2	chr5:97259772-97260470	GM12878	blood:	n/a	n/a
31	CHD2	chr5:97386435-97386634	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr5:97321869-97322189	GM12878	blood:	n/a	chr5:97322002-97322018 chr5:97321996-97322017 chr5:97322001-97322019
33	CTCF	chr5:97296840-97296990	K562	blood:	n/a	n/a
34	CTCF	chr5:97366100-97366250	GM12874	blood:	n/a	n/a
35	CTCF	chr5:97389453-97389482	GM10248	blood:	n/a	n/a
36	CTCF	chr5:97321900-97322102	Fibrobl	skin:	n/a	chr5:97322002-97322018 chr5:97321996-97322017 chr5:97322001-97322019
37	CTCF	chr5:97366100-97366250	GM12871	blood:	n/a	n/a
38	CTCF	chr5:97366140-97366290	GM12873	blood:	n/a	n/a
39	CTCF	chr5:97366100-97366250	WI-38	lung:	n/a	n/a
40	CTCF	chr5:97321980-97322130	AG10803	skin:	n/a	chr5:97322002-97322018 chr5:97321996-97322017 chr5:97322001-97322019
41	CTCF	chr5:97366120-97366270	HA-sp	spinal cord:	n/a	n/a
42	CTCF	chr5:97366120-97366270	GM12873	blood:	n/a	n/a
43	CTCF	chr5:97321940-97322090	AG10803	skin:	n/a	chr5:97322002-97322018 chr5:97321996-97322017 chr5:97322001-97322019
44	CTCF	chr5:97366140-97366290	BE2_C	brain:	n/a	n/a
45	CTCF	chr5:97366140-97366290	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr5:97366040-97366190	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr5:97366140-97366290	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr5:97366080-97366230	HFF	foreskin:	n/a	n/a
49	CTCF	chr5:97366100-97366250	A549	lung:	n/a	n/a
50	CTCF	chr5:97321940-97322090	HMF	breast:	n/a	chr5:97322002-97322018 chr5:97321996-97322017 chr5:97322001-97322019

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:97315689-97315739	HCT-116	colon:	n/a
2	chr5:97315689-97315739	HL-60	blood:	n/a
3	chr5:97315689-97315739	SAEC	small airway:	n/a
4	chr5:97315689-97315739	HMEC	breast:	n/a
5	chr5:97315689-97315739	AG04450	lung:	fetal
6	chr5:97315689-97315739	SKMC	muscle:	n/a
7	chr5:97315689-97315739	NHBE	bronchial:	n/a
8	chr5:97315689-97315739	Jurkat	blood:	n/a
9	chr5:97315689-97315739	GM12878	blood:	n/a
10	chr5:97315689-97315739	PrEC	prostate:	n/a
11	chr5:97315689-97315739	SK-N-SH	brain:	n/a
12	chr5:97315689-97315739	NHDF-neo	bronchial:	n/a
13	chr5:97315689-97315739	HPAEpiC	pulmonary alveolar:	n/a
14	chr5:97315689-97315739	GM12891	blood:	n/a
15	chr5:97315689-97315739	GM06990	blood:	n/a
16	chr5:97315689-97315739	SK-N-MC	brain:	n/a
17	chr5:97315689-97315739	HEEpiC	esophagus:	n/a
18	chr5:97315689-97315739	Hepatocyte	liver:	n/a
19	chr5:97315689-97315739	K562	blood:	n/a
20	chr5:97315689-97315739	HCM	heart:	n/a
21	chr5:97315689-97315739	U87	brain:	n/a
22	chr5:97315689-97315739	H1-hESC	embryonic stem cell:	embryo
23	chr5:97315689-97315739	HUVEC	blood vessel:	n/a
24	chr5:97315689-97315739	T-47D	breast:	n/a
25	chr5:97315689-97315739	PFSK-1	brain:	n/a
26	chr5:97315689-97315739	HepG2	liver:	n/a
27	chr5:97315689-97315739	Caco-2	colon:	n/a
28	chr5:97315689-97315739	AG04449	skin:	fetal
29	chr5:97315689-97315739	NT2-D1	testis:	n/a
30	chr5:97315689-97315739	HRE	kidney:	n/a
31	chr5:97315689-97315739	IMR90	lung:	fetal
32	chr5:97315689-97315739	LNCaP	prostate:	n/a
33	chr5:97315689-97315739	AG09309	skin:	n/a
34	chr5:97315689-97315739	MCF10A-Er-Src	breast:	n/a
35	chr5:97315689-97315739	Hela-S3	cervix:	n/a
36	chr5:97315689-97315739	SK-N-SH_RA	brain:	n/a
37	chr5:97315689-97315739	ECC-1	luminal epithelium:	n/a
38	chr5:97315689-97315739	ovcar-3	ovarian:	n/a
39	chr5:97315689-97315739	GM12892	blood:	n/a
40	chr5:97315689-97315739	PANC-1	pancreas:	n/a
41	chr5:97315689-97315739	MCF-7	breast:	n/a
42	chr5:97315689-97315739	NH-A	brain:	n/a
43	chr5:97315689-97315739	HRPEpiC	eye:	n/a
44	chr5:97315689-97315739	HCPEpiC	choroid plexus:	n/a
45	chr5:97315689-97315739	HNPCEpiC	eye:	n/a
46	chr5:97315689-97315739	AG10803	skin:	n/a
47	chr5:97315689-97315739	HIPEpiC	eye:	n/a
48	chr5:97315689-97315739	HEK293	kidney:	embryo
49	chr5:97315689-97315739	BJ	skin:	n/a
50	chr5:97315689-97315739	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:97331985..97334979-chr5:97337146..97339738,2	K562	blood:
2	chr5:97331985..97334979-chr5:97337146..97339738,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHD1-2	chr5:97429104-97429275	XLOC_004935
2	lnc-CHD1-2	chr5:97421964-97421988	XLOC_004935

Variant related genes	Relation type
ENSG00000249101	TF binding region
ENSG00000249101	CpG island
ARFIP1	miRNA target sites
CTLA4	miRNA target sites

Extended variants
information (count: 3817 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:3817 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192238982	chr5:97259864-97259865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs541847628	chr5:97259959-97259960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs112876676	chr5:97260041-97260042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs1423319	chr5:97260047-97260048	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs527419710	chr5:97260103-97260104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546388555	chr5:97260132-97260133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539670456	chr5:97260162-97260163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs10078008	chr5:97260217-97260218	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs566512599	chr5:97260250-97260251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs149722548	chr5:97260261-97260262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568777249	chr5:97260282-97260283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs1423320	chr5:97260358-97260359	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs369051185	chr5:97260388-97260389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182766884	chr5:97260411-97260412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs541606868	chr5:97260508-97260509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs369381573	chr5:97260509-97260510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs28474721	chr5:97264602-97264603	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs575337052	chr5:97264638-97264639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181753030	chr5:97264658-97264659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs111958649	chr5:97264697-97264698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150783722	chr5:97264714-97264715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs539810606	chr5:97264716-97264717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564563381	chr5:97264755-97264756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs139653333	chr5:97264767-97264768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs187359473	chr5:97264798-97264799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562641216	chr5:97264900-97264901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs562157003	chr5:97264902-97264903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs201422248	chr5:97264996-97264997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79860406	chr5:97264999-97265000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs145485658	chr5:97265004-97265005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs138613786	chr5:97265028-97265029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs115268391	chr5:97265048-97265049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528005737	chr5:97265049-97265050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs147267027	chr5:97265056-97265057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs533240853	chr5:97265075-97265076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs17653177	chr5:97265092-97265093	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs538278917	chr5:97265112-97265113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs190502752	chr5:97265171-97265172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556380641	chr5:97265192-97265193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs12108846	chr5:97265230-97265231	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs140787406	chr5:97265244-97265245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs563295372	chr5:97265283-97265284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs572775351	chr5:97265344-97265345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs559822465	chr5:97265352-97265353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs149776167	chr5:97265353-97265354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374028534	chr5:97265379-97265380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs180928178	chr5:97265402-97265403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs576751049	chr5:97265407-97265408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs544239170	chr5:97265419-97265420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs562418469	chr5:97265451-97265452	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21611746	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:174 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97259800-97260600	Enhancers	GM12878-XiMat	blood
2	chr5:97264600-97265800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr5:97265200-97265800	Enhancers	NHDF-Ad	bronchial
4	chr5:97265800-97271800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr5:97271800-97272200	Enhancers	Adipose Nuclei	Adipose
6	chr5:97271800-97272200	Enhancers	Brain Cingulate Gyrus	brain
7	chr5:97271800-97272200	Enhancers	Fetal Lung	lung
8	chr5:97271800-97272400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr5:97271800-97272400	Enhancers	Brain Substantia Nigra	brain
10	chr5:97271800-97272600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr5:97271800-97272800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr5:97272000-97272200	Enhancers	NHDF-Ad	bronchial
13	chr5:97272000-97272400	Enhancers	Brain Angular Gyrus	brain
14	chr5:97272000-97272800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr5:97273200-97274400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr5:97291400-97291600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr5:97297800-97298200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr5:97297800-97298200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr5:97297800-97298200	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr5:97307800-97308400	Enhancers	Duodenum Mucosa	Duodenum
21	chr5:97310600-97321800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr5:97313200-97313800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr5:97313800-97315000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr5:97314800-97321400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr5:97315000-97315600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr5:97315000-97316000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr5:97315000-97316400	Enhancers	Fetal Lung	lung
28	chr5:97315400-97316600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr5:97315600-97316000	Enhancers	Fetal Stomach	stomach
30	chr5:97315600-97316800	Enhancers	HUVEC	blood vessel
31	chr5:97315800-97316200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr5:97316200-97321600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr5:97316400-97316600	Weak transcription	Fetal Lung	lung
34	chr5:97318200-97318400	Enhancers	Fetal Lung	lung
35	chr5:97321400-97321800	Enhancers	Osteobl	bone
36	chr5:97321400-97322400	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr5:97321400-97322400	Enhancers	Muscle Satellite Cultured Cells	--
38	chr5:97321400-97322600	Enhancers	NHDF-Ad	bronchial
39	chr5:97321600-97321800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr5:97321600-97321800	Enhancers	NH-A	brain
41	chr5:97321800-97322000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr5:97321800-97322200	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr5:97321800-97322200	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr5:97321800-97322200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr5:97321800-97322200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr5:97321800-97322200	Enhancers	HSMM	muscle
47	chr5:97321800-97322200	Flanking Active TSS	NH-A	brain
48	chr5:97321800-97322200	Flanking Active TSS	Osteobl	bone
49	chr5:97322000-97322200	Enhancers	NHLF	lung
50	chr5:97322200-97322400	Enhancers	NH-A	brain

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