Variant report

Variant	nsv878696
Chromosome Location	chr4:10488726-10520693
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:92)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:92 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr4:10497303-10497547	K562	blood:	n/a	n/a
2	BHLHE40	chr4:10497245-10497653	K562	blood:	n/a	n/a
3	BHLHE40	chr4:10497301-10497575	HepG2	liver:	n/a	n/a
4	BHLHE40	chr4:10511488-10511709	K562	blood:	n/a	n/a
5	CTCF	chr4:10498590-10498665	LNCaP	prostate:	n/a	n/a
6	CTCF	chr4:10511563-10511623	K562	blood:	n/a	n/a
7	CTCF	chr4:10511467-10511742	K562	blood:	n/a	chr4:10511482-10511491
8	CTCF	chr4:10511546-10511620	MCF-7	breast:	n/a	n/a
9	CTCF	chr4:10494900-10495050	GM12866	blood:	n/a	n/a
10	CUX1	chr4:10493323-10493330	GM12878	blood:	n/a	n/a
11	CUX1	chr4:10496834-10496892	K562	blood:	n/a	n/a
12	ELK1	chr4:10490115-10490135	K562	blood:	n/a	n/a
13	EP300	chr4:10493058-10493292	K562	blood:	n/a	n/a
14	EP300	chr4:10497832-10498245	H1-hESC	embryonic stem cell:	n/a	n/a
15	FOS	chr4:10495512-10495703	MCF10A-Er-Src	breast:	n/a	n/a
16	GTF2F1	chr4:10497914-10498109	H1-hESC	embryonic stem cell:	n/a	n/a
17	GTF2F1	chr4:10497335-10497596	H1-hESC	embryonic stem cell:	n/a	n/a
18	HDAC2	chr4:10497841-10498272	H1-hESC	embryonic stem cell:	n/a	n/a
19	HDAC2	chr4:10497903-10498216	H1-hESC	embryonic stem cell:	n/a	n/a
20	IRF1	chr4:10493125-10493434	K562	blood:	n/a	n/a
21	IRF1	chr4:10520196-10520256	K562	blood:	n/a	n/a
22	MAFK	chr4:10502406-10502524	HepG2	liver:	n/a	chr4:10502415-10502430
23	MAFK	chr4:10502354-10502519	HepG2	liver:	n/a	chr4:10502415-10502430
24	MAX	chr4:10497322-10497571	K562	blood:	n/a	n/a
25	MAX	chr4:10511352-10511718	K562	blood:	n/a	chr4:10511547-10511556 chr4:10511545-10511553 chr4:10511545-10511558 chr4:10511546-10511557 chr4:10511547-10511556 chr4:10511545-10511558
26	MAX	chr4:10507841-10508023	NB4	blood:	n/a	n/a
27	MAX	chr4:10497839-10498307	H1-hESC	embryonic stem cell:	n/a	n/a
28	MAX	chr4:10497967-10498227	H1-hESC	embryonic stem cell:	n/a	n/a
29	MAX	chr4:10497341-10498219	H1-hESC	embryonic stem cell:	n/a	n/a
30	MYC	chr4:10511549-10511745	K562	blood:	n/a	n/a
31	NANOG	chr4:10497861-10498224	H1-hESC	embryonic stem cell:	n/a	n/a
32	NANOG	chr4:10497838-10498217	H1-hESC	embryonic stem cell:	n/a	n/a
33	NFE2	chr4:10497358-10497541	GM12878	blood:	n/a	n/a
34	POLR2A	chr4:10498143-10498159	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr4:10514325-10514370	MCF10A-Er-Src	breast:	n/a	n/a
36	POLR2A	chr4:10488769-10488918	ProgFib	skin:	n/a	n/a
37	POLR2A	chr4:10520178-10520196	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr4:10489304-10489434	GM12878	blood:	n/a	n/a
39	POLR2A	chr4:10496651-10496704	MCF10A-Er-Src	breast:	n/a	n/a
40	RAD21	chr4:10497801-10498221	H1-hESC	embryonic stem cell:	n/a	n/a
41	RAD21	chr4:10511529-10511656	K562	blood:	n/a	n/a
42	RAD21	chr4:10511459-10511710	H1-hESC	embryonic stem cell:	n/a	chr4:10511485-10511495
43	RAD21	chr4:10511508-10511677	K562	blood:	n/a	n/a
44	RCOR1	chr4:10497329-10497525	K562	blood:	n/a	n/a
45	REST	chr4:10489041-10489373	PFSK-1	brain:	n/a	n/a
46	REST	chr4:10489019-10489339	PFSK-1	brain:	n/a	n/a
47	REST	chr4:10509766-10509980	H1-hESC	embryonic stem cell:	n/a	n/a
48	REST	chr4:10489062-10489305	K562	blood:	n/a	n/a
49	RFX5	chr4:10497309-10497434	K562	blood:	n/a	n/a
50	SMC3	chr4:10511521-10511640	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10498037-10498087	HCT-116	colon:	n/a
2	chr4:10498037-10498087	AoSMC	blood vessel:	n/a
3	chr4:10498037-10498087	Hepatocyte	liver:	n/a
4	chr4:10498037-10498087	HPAEpiC	pulmonary alveolar:	n/a
5	chr4:10498037-10498087	HepG2	liver:	n/a
6	chr4:10498037-10498087	GM12892	blood:	n/a
7	chr4:10498037-10498087	HEEpiC	esophagus:	n/a
8	chr4:10498037-10498087	GM06990	blood:	n/a
9	chr4:10498037-10498087	AG10803	skin:	n/a
10	chr4:10498037-10498087	Jurkat	blood:	n/a
11	chr4:10498037-10498087	HMEC	breast:	n/a
12	chr4:10498037-10498087	SK-N-SH_RA	brain:	n/a
13	chr4:10498037-10498087	U87	brain:	n/a
14	chr4:10498037-10498087	AG04450	lung:	fetal
15	chr4:10498037-10498087	GM12891	blood:	n/a
16	chr4:10498037-10498087	Caco-2	colon:	n/a
17	chr4:10498037-10498087	HAEpiC	amniotic membrane:	n/a
18	chr4:10498037-10498087	BE2_C	brain:	n/a
19	chr4:10498037-10498087	ovcar-3	ovarian:	n/a
20	chr4:10498037-10498087	HCPEpiC	choroid plexus:	n/a
21	chr4:10498037-10498087	NHDF-neo	bronchial:	n/a
22	chr4:10498037-10498087	HEK293	kidney:	embryo
23	chr4:10498037-10498087	T-47D	breast:	n/a
24	chr4:10498037-10498087	H1-hESC	embryonic stem cell:	embryo
25	chr4:10498037-10498087	SK-N-MC	brain:	n/a
26	chr4:10498037-10498087	GM12878	blood:	n/a
27	chr4:10498037-10498087	LNCaP	prostate:	n/a
28	chr4:10498037-10498087	HCF	heart:	n/a
29	chr4:10498037-10498087	CMK	blood:	n/a
30	chr4:10498037-10498087	MCF-7	breast:	n/a
31	chr4:10498037-10498087	SK-N-SH	brain:	n/a
32	chr4:10498037-10498087	AG09309	skin:	n/a
33	chr4:10498037-10498087	PANC-1	pancreas:	n/a
34	chr4:10498037-10498087	A549	lung:	n/a
35	chr4:10498037-10498087	HRE	kidney:	n/a
36	chr4:10498037-10498087	ProgFib	skin:	n/a
37	chr4:10498037-10498087	K562	blood:	n/a
38	chr4:10498037-10498087	IMR90	lung:	fetal
39	chr4:10498037-10498087	HL-60	blood:	n/a
40	chr4:10498037-10498087	NH-A	brain:	n/a
41	chr4:10498037-10498087	ECC-1	luminal epithelium:	n/a
42	chr4:10498037-10498087	SKMC	muscle:	n/a
43	chr4:10498037-10498087	PrEC	prostate:	n/a
44	chr4:10498037-10498087	BJ	skin:	n/a
45	chr4:10498037-10498087	NHBE	bronchial:	n/a
46	chr4:10498037-10498087	HRPEpiC	eye:	n/a
47	chr4:10498037-10498087	HIPEpiC	eye:	n/a
48	chr4:10498037-10498087	HCM	heart:	n/a
49	chr4:10498037-10498087	NT2-D1	testis:	n/a
50	chr4:10498037-10498087	RPTEC	kidney:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:10489847..10492535-chr4:10493316..10497082,4	K562	blood:
2	chr4:10483661..10485837-chr4:10489240..10491538,2	K562	blood:
3	chr4:10489847..10492535-chr4:10493316..10497082,4	K562	blood:
4	chr4:10483820..10485837-chr4:10490038..10492249,2	K562	blood:
5	chr4:10489847..10492535-chr4:10493316..10495674,3	K562	blood:
6	chr4:10119097..10123564-chr4:10520690..10524781,5	K562	blood:
7	chr4:10489847..10492535-chr4:10493316..10495674,3	K562	blood:
8	chr4:10511298..10512999-chr4:10531999..10534299,2	K562	blood:
9	chr4:10513028..10514802-chr4:10517875..10519589,2	K562	blood:
10	chr4:10509410..10511877-chr4:10515360..10517382,2	K562	blood:
11	chr4:10509410..10511877-chr4:10515360..10517382,2	K562	blood:
12	chr4:10118463..10120223-chr4:10516574..10518474,2	K562	blood:
13	chr4:10120550..10123104-chr4:10488243..10490755,2	K562	blood:
14	chr4:10109397..10110994-chr4:10487986..10490652,2	K562	blood:
15	chr4:10119129..10122077-chr4:10500850..10502742,2	K562	blood:

No data

Variant related genes	Relation type
CLNK	TF binding region
CLNK	CpG island
ENSG00000109684	chromatin interactions
ENSG00000071127	chromatin interactions

Extended variants
information (count: 1258 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:1258 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370725402	chr4:10489214-10489215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs112982580	chr4:10489215-10489216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs116646151	chr4:10489225-10489226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs75675244	chr4:10489246-10489247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs78445114	chr4:10489247-10489248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559597965	chr4:10489254-10489255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573282008	chr4:10489257-10489258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs574829261	chr4:10489276-10489277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs183200436	chr4:10489278-10489279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs79719977	chr4:10489302-10489303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs151018213	chr4:10489325-10489326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs35057037	chr4:10489338-10489339	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs562454273	chr4:10489390-10489391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186008946	chr4:10489395-10489396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs7658580	chr4:10489396-10489397	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs140692336	chr4:10489417-10489418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs530938915	chr4:10489439-10489440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs551137022	chr4:10489526-10489527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs374251013	chr4:10489546-10489547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs144246684	chr4:10489548-10489549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs13130674	chr4:10489600-10489601	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs4530623	chr4:10489629-10489630	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs7686391	chr4:10489688-10489689	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs183342334	chr4:10489698-10489699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528290661	chr4:10489716-10489717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569614425	chr4:10489718-10489719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs73090100	chr4:10489826-10489827	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs557898971	chr4:10489834-10489835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs7685344	chr4:10489855-10489856	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs34601639	chr4:10489856-10489857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs187882460	chr4:10489864-10489865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534011617	chr4:10489888-10489889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147797505	chr4:10489911-10489912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573464008	chr4:10489949-10489950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535710081	chr4:10489959-10489960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73226433	chr4:10489988-10489989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544045204	chr4:10490028-10490029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs141233406	chr4:10490086-10490087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577888598	chr4:10490147-10490148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544975254	chr4:10490159-10490160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550872962	chr4:10490170-10490171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559864924	chr4:10490182-10490183	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs7685992	chr4:10490218-10490219	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs549058381	chr4:10490233-10490234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192721490	chr4:10490243-10490244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529504020	chr4:10490277-10490278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10488945	chr4:10490278-10490279	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs111475369	chr4:10490296-10490297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539708823	chr4:10490434-10490435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138900887	chr4:10490484-10490485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD

Chromatin state (count:138 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10489200-10489400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr4:10489200-10489600	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr4:10489600-10492800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:10490000-10490200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr4:10490400-10497800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:10490800-10491200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr4:10491200-10491600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr4:10491600-10491800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr4:10491800-10493800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr4:10492000-10492200	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr4:10492800-10493000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr4:10492800-10493400	Enhancers	K562	blood
13	chr4:10493000-10497000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr4:10493400-10497400	Weak transcription	K562	blood
15	chr4:10493800-10494400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr4:10493800-10494400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr4:10493800-10494600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr4:10494000-10494400	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr4:10494200-10494600	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr4:10494400-10494600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
21	chr4:10494400-10497000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr4:10494600-10495400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr4:10494600-10496800	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr4:10495400-10495600	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
25	chr4:10495400-10495600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr4:10495600-10495800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr4:10495800-10496000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
28	chr4:10496600-10497200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
29	chr4:10496600-10497400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
30	chr4:10496800-10497400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
31	chr4:10496800-10497600	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr4:10496800-10497600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
33	chr4:10496800-10497600	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr4:10496800-10497600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
35	chr4:10497000-10497200	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
36	chr4:10497000-10497600	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr4:10497000-10497600	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr4:10497000-10497600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr4:10497000-10497800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr4:10497000-10498800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr4:10497000-10499600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr4:10497200-10497600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr4:10497200-10497600	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr4:10497200-10498200	Enhancers	H9 Cell Line	embryonic stem cell
45	chr4:10497400-10497600	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr4:10497400-10499200	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr4:10497400-10499400	Enhancers	K562	blood
48	chr4:10497600-10497800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
49	chr4:10497600-10497800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
50	chr4:10497600-10498000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell

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