Variant report

Variant	nsv4924
Chromosome Location	chr5:96391451-96437233
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:308)
CpG islands
(count:305)
Chromatin interactive
region (count:14)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:96424587-96424845	K562	blood:	n/a	n/a
2	ARID3A	chr5:96407458-96407610	K562	blood:	n/a	n/a
3	ARID3A	chr5:96407023-96407145	K562	blood:	n/a	n/a
4	ATF1	chr5:96407587-96407588	K562	blood:	n/a	n/a
5	ATF1	chr5:96424591-96425404	K562	blood:	n/a	n/a
6	ATF2	chr5:96430546-96431435	GM12878	blood:	n/a	n/a
7	ATF2	chr5:96430604-96431433	GM12878	blood:	n/a	n/a
8	ATF3	chr5:96425318-96425532	K562	blood:	n/a	n/a
9	BACH1	chr5:96424894-96425343	K562	blood:	n/a	n/a
10	BATF	chr5:96430639-96431326	GM12878	blood:	n/a	chr5:96430968-96430978 chr5:96430967-96430978 chr5:96430947-96430958
11	BATF	chr5:96430694-96431298	GM12878	blood:	n/a	chr5:96430968-96430978 chr5:96430967-96430978 chr5:96430947-96430958
12	BCL11A	chr5:96430693-96431212	GM12878	blood:	n/a	chr5:96430902-96430911
13	BCL11A	chr5:96430751-96431093	GM12878	blood:	n/a	chr5:96430902-96430911
14	BCL3	chr5:96430753-96431143	GM12878	blood:	n/a	chr5:96430902-96430911
15	BCLAF1	chr5:96430683-96431174	GM12878	blood:	n/a	chr5:96430902-96430911
16	BCLAF1	chr5:96430534-96431334	GM12878	blood:	n/a	chr5:96430902-96430911
17	BHLHE40	chr5:96430676-96431125	GM12878	blood:	n/a	n/a
18	BHLHE40	chr5:96424892-96425674	K562	blood:	n/a	chr5:96425411-96425424
19	CBX3	chr5:96420299-96420625	K562	blood:	n/a	n/a
20	CBX3	chr5:96424434-96425591	K562	blood:	n/a	n/a
21	CCNT2	chr5:96425020-96425392	K562	blood:	n/a	n/a
22	CEBPB	chr5:96413593-96413613	K562	blood:	n/a	n/a
23	CEBPB	chr5:96399274-96399287	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr5:96430810-96431062	GM12878	blood:	n/a	n/a
25	CEBPB	chr5:96413136-96413388	K562	blood:	n/a	n/a
26	CEBPB	chr5:96430561-96431422	GM12878	blood:	n/a	n/a
27	CEBPB	chr5:96414719-96415001	IMR90	lung:	n/a	n/a
28	CEBPB	chr5:96425212-96425529	K562	blood:	n/a	n/a
29	CEBPB	chr5:96413111-96413398	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPD	chr5:96424449-96424938	K562	blood:	n/a	n/a
31	CHD1	chr5:96431214-96431295	GM12878	blood:	n/a	n/a
32	CTCF	chr5:96397465-96397512	GM19240	blood:	n/a	n/a
33	CTCF	chr5:96397447-96397519	GM19238	blood:	n/a	n/a
34	CTCF	chr5:96397416-96397584	K562	blood:	n/a	n/a
35	CTCF	chr5:96397480-96397630	K562	blood:	n/a	n/a
36	CTCF	chr5:96397328-96397597	GM12878	blood:	n/a	n/a
37	CTCF	chr5:96421574-96421601	Lung_OC	lung:	n/a	n/a
38	CTCF	chr5:96397438-96397540	GM12892	blood:	n/a	n/a
39	CTCF	chr5:96407004-96407081	NHEK	skin:	n/a	n/a
40	CTCF	chr5:96397500-96397650	BE2_C	brain:	n/a	n/a
41	CTCF	chr5:96397432-96397562	GM12878	blood:	n/a	n/a
42	CTCF	chr5:96397440-96397590	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr5:96406902-96406974	GM10248	blood:	n/a	n/a
44	CTCF	chr5:96397323-96397658	K562	blood:	n/a	n/a
45	CTCF	chr5:96397320-96397470	BE2_C	brain:	n/a	n/a
46	CTCF	chr5:96391820-96391970	A549	lung:	n/a	n/a
47	CTCF	chr5:96425040-96425190	GM12864	blood:	n/a	n/a
48	CTCF	chr5:96433498-96433513	Spleen_OC	spleen:	n/a	n/a
49	CUX1	chr5:96397493-96397675	K562	blood:	n/a	n/a
50	E2F4	chr5:96406915-96407134	MCF10A-Er-Src	breast:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:96432518-96432568	T-47D	breast:	n/a
2	chr5:96421037-96421087	H1-hESC	embryonic stem cell:	embryo
3	chr5:96401915-96401965	NHBE	bronchial:	n/a
4	chr5:96421037-96421087	U87	brain:	n/a
5	chr5:96401915-96401965	AG04449	skin:	fetal
6	chr5:96430437-96430487	HMEC	breast:	n/a
7	chr5:96432518-96432568	HCT-116	colon:	n/a
8	chr5:96421245-96421295	ECC-1	luminal epithelium:	n/a
9	chr5:96432518-96432568	CMK	blood:	n/a
10	chr5:96430437-96430487	HCT-116	colon:	n/a
11	chr5:96401915-96401965	HL-60	blood:	n/a
12	chr5:96421245-96421295	AG10803	skin:	n/a
13	chr5:96421037-96421087	SKMC	muscle:	n/a
14	chr5:96401915-96401965	HRPEpiC	eye:	n/a
15	chr5:96432518-96432568	GM06990	blood:	n/a
16	chr5:96430437-96430487	SKMC	muscle:	n/a
17	chr5:96432518-96432568	AG04450	lung:	fetal
18	chr5:96421037-96421087	NH-A	brain:	n/a
19	chr5:96401915-96401965	Hepatocyte	liver:	n/a
20	chr5:96421245-96421295	BE2_C	brain:	n/a
21	chr5:96432518-96432568	HIPEpiC	eye:	n/a
22	chr5:96421037-96421087	IMR90	lung:	fetal
23	chr5:96430437-96430487	AG04449	skin:	fetal
24	chr5:96430437-96430487	HCM	heart:	n/a
25	chr5:96401915-96401965	HEEpiC	esophagus:	n/a
26	chr5:96430437-96430487	GM19239	blood:	n/a
27	chr5:96421245-96421295	AoSMC	blood vessel:	n/a
28	chr5:96430437-96430487	U87	brain:	n/a
29	chr5:96401915-96401965	Jurkat	blood:	n/a
30	chr5:96430437-96430487	HEK293	kidney:	embryo
31	chr5:96401915-96401965	NH-A	brain:	n/a
32	chr5:96421245-96421295	SKMC	muscle:	n/a
33	chr5:96401915-96401965	CMK	blood:	n/a
34	chr5:96401915-96401965	A549	lung:	n/a
35	chr5:96421245-96421295	HPAEpiC	pulmonary alveolar:	n/a
36	chr5:96421037-96421087	BE2_C	brain:	n/a
37	chr5:96421037-96421087	A549	lung:	n/a
38	chr5:96421245-96421295	Hepatocyte	liver:	n/a
39	chr5:96430437-96430487	ECC-1	luminal epithelium:	n/a
40	chr5:96421245-96421295	A549	lung:	n/a
41	chr5:96430437-96430487	AG10803	skin:	n/a
42	chr5:96430437-96430487	IMR90	lung:	fetal
43	chr5:96401915-96401965	AG10803	skin:	n/a
44	chr5:96432518-96432568	HPAEpiC	pulmonary alveolar:	n/a
45	chr5:96432518-96432568	HCF	heart:	n/a
46	chr5:96421245-96421295	HEEpiC	esophagus:	n/a
47	chr5:96421037-96421087	HCT-116	colon:	n/a
48	chr5:96421037-96421087	CMK	blood:	n/a
49	chr5:96421037-96421087	HL-60	blood:	n/a
50	chr5:96401915-96401965	NHDF-neo	bronchial:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:96425190..96428341-chr5:96429686..96433552,4	K562	blood:
2	chr5:96425765..96427339-chr5:96454933..96458511,3	K562	blood:
3	chr5:96413541..96415661-chr5:96445428..96448359,2	MCF-7	breast:
4	chr5:96396537..96398150-chr5:96400211..96401928,2	K562	blood:
5	chr5:96422481..96423221-chr5:96497763..96498668,2	K562	blood:
6	chr5:96396537..96398150-chr5:96400211..96401928,2	K562	blood:
7	chr5:96422091..96424070-chr5:96427925..96429531,2	K562	blood:
8	chr5:96431878..96433663-chr5:96441346..96442854,2	K562	blood:
9	chr5:96419619..96421604-chr5:96424040..96426656,2	K562	blood:
10	chr5:96425190..96428341-chr5:96429686..96433552,4	K562	blood:
11	chr5:96414990..96416706-chr5:96466146..96468878,2	MCF-7	breast:
12	chr5:96422091..96424070-chr5:96427925..96429531,2	K562	blood:
13	chr5:96405505..96407862-chr5:96413976..96415782,2	K562	blood:
14	chr5:96405505..96407862-chr5:96413976..96415782,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LNPEP-4	chr5:96396070-96396412	expReg_chr5_5489_+
2	lnc-LNPEP-2	chr5:96391087-96391521	expReg_chr5_5481_+
3	lnc-LNPEP-3	chr5:96395285-96395811	expReg_chr5_5487_+

No data

Variant related genes	Relation type
ENSG00000251606	TF binding region
SETP22	TF binding region
ENSG00000251606	CpG island
SETP22	CpG island
ENSG00000251606	chromatin interactions

Extended variants
information (count: 1783 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1783 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535068472	chr5:96391489-96391490	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs546681789	chr5:96391513-96391514	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs571579897	chr5:96391574-96391575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs538774494	chr5:96391580-96391581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs421173	chr5:96391590-96391591	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs188806253	chr5:96391612-96391613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536431675	chr5:96391627-96391628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs57359849	chr5:96391636-96391637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554881121	chr5:96391642-96391643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573196434	chr5:96391678-96391679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150105285	chr5:96391702-96391703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138435068	chr5:96391703-96391704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192188411	chr5:96391762-96391763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185502767	chr5:96391790-96391791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148831293	chr5:96391798-96391799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs530767456	chr5:96391812-96391813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs199695263	chr5:96391837-96391838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116405853	chr5:96391848-96391849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561020231	chr5:96391896-96391897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573280712	chr5:96391926-96391927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190429940	chr5:96391938-96391939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546840703	chr5:96391942-96391943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs571577237	chr5:96391945-96391946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs143443183	chr5:96391968-96391969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs180862450	chr5:96391990-96391991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568998458	chr5:96392001-96392002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536494026	chr5:96392016-96392017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554745911	chr5:96392018-96392019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs78977991	chr5:96392019-96392020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566683147	chr5:96392020-96392021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556881287	chr5:96392026-96392027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs149568695	chr5:96392031-96392032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112621507	chr5:96392040-96392041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113353622	chr5:96392058-96392059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs59654717	chr5:96392067-96392068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542250738	chr5:96392073-96392074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs370663524	chr5:96392082-96392083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577602019	chr5:96392089-96392090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544981399	chr5:96392092-96392093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs556827041	chr5:96392197-96392198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575709884	chr5:96392199-96392200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575416919	chr5:96392211-96392212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542706400	chr5:96392222-96392223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561084578	chr5:96392316-96392317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188600434	chr5:96392334-96392335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138231667	chr5:96392354-96392355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs143688175	chr5:96392357-96392358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146374932	chr5:96392364-96392365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138795398	chr5:96392387-96392388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs541712837	chr5:96392398-96392399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:455 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96386800-96397800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr5:96395600-96395800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr5:96395600-96395800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr5:96395800-96397800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr5:96395800-96398800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr5:96397400-96398000	Enhancers	Psoas Muscle	Psoas
7	chr5:96397400-96398200	Enhancers	Skeletal Muscle Male	skeletal muscle
8	chr5:96397400-96398400	Enhancers	Skeletal Muscle Female	skeletal muscle
9	chr5:96397400-96399800	Enhancers	Fetal Muscle Leg	muscle
10	chr5:96397600-96398000	Enhancers	Fetal Muscle Trunk	muscle
11	chr5:96397600-96398200	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr5:96397600-96398200	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr5:96397800-96398000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:96397800-96398000	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr5:96397800-96398000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr5:96397800-96398200	Enhancers	H1 Cell Line	embryonic stem cell
17	chr5:96397800-96398200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr5:96397800-96398200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr5:96398000-96398200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr5:96398000-96401000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr5:96398200-96400800	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr5:96398200-96401000	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr5:96398400-96401200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr5:96398800-96399600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr5:96398800-96399800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr5:96399000-96399600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr5:96399200-96399600	Enhancers	Fetal Kidney	kidney
28	chr5:96399600-96402800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr5:96399600-96407400	Weak transcription	Fetal Kidney	kidney
30	chr5:96399800-96401000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr5:96399800-96405800	Weak transcription	Fetal Muscle Leg	muscle
32	chr5:96400400-96400800	Active TSS	GM12878-XiMat	blood
33	chr5:96400600-96401000	Active TSS	HSMM	muscle
34	chr5:96400600-96401400	Enhancers	Primary T cells from cord blood	blood
35	chr5:96400800-96401600	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr5:96400800-96401800	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr5:96400800-96402400	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr5:96400800-96403000	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr5:96401000-96401400	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr5:96401000-96401600	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr5:96401000-96401800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr5:96401200-96401400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr5:96401200-96401400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr5:96401200-96401600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr5:96401200-96403200	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr5:96401400-96403000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr5:96401800-96402800	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr5:96402800-96403400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr5:96402800-96403400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr5:96403000-96403200	Enhancers	HUES64 Cell Line	embryonic stem cell

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