Variant report

Variant	nsv830013
Chromosome Location	chr4:97033125-97204291
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:482)
CpG islands
(count:366)
Chromatin interactive
region (count:15)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr4:97181320-97181623	GM12878	blood:	n/a	n/a
2	CBX3	chr4:97091368-97091657	K562	blood:	n/a	n/a
3	CBX3	chr4:97091295-97091494	K562	blood:	n/a	n/a
4	CEBPB	chr4:97071933-97071937	K562	blood:	n/a	n/a
5	CEBPB	chr4:97103049-97103464	IMR90	lung:	n/a	chr4:97103174-97103185
6	CEBPB	chr4:97058473-97058673	A549	lung:	n/a	chr4:97058529-97058540 chr4:97058530-97058541
7	CEBPB	chr4:97033522-97033611	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr4:97092306-97092550	A549	lung:	n/a	chr4:97092391-97092402
9	CEBPB	chr4:97103081-97103335	HepG2	liver:	n/a	chr4:97103174-97103185
10	CEBPB	chr4:97181245-97181515	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr4:97196970-97197200	IMR90	lung:	n/a	chr4:97197086-97197097 chr4:97197086-97197099 chr4:97197088-97197099
12	CEBPB	chr4:97092252-97092583	IMR90	lung:	n/a	chr4:97092391-97092402
13	CEBPB	chr4:97121791-97122057	HepG2	liver:	n/a	chr4:97121932-97121945 chr4:97121932-97121945 chr4:97121933-97121944
14	CEBPB	chr4:97040249-97040449	HepG2	liver:	n/a	chr4:97040363-97040374 chr4:97040363-97040376 chr4:97040364-97040375
15	CEBPB	chr4:97169823-97170116	IMR90	lung:	n/a	chr4:97169952-97169963
16	CEBPB	chr4:97092270-97092566	H1-hESC	embryonic stem cell:	n/a	chr4:97092391-97092402
17	CEBPB	chr4:97121782-97122027	K562	blood:	n/a	chr4:97121932-97121945 chr4:97121932-97121945 chr4:97121933-97121944
18	CEBPB	chr4:97103129-97103234	H1-hESC	embryonic stem cell:	n/a	chr4:97103174-97103185
19	CEBPB	chr4:97169804-97170043	HepG2	liver:	n/a	chr4:97169952-97169963
20	CEBPB	chr4:97092257-97092575	K562	blood:	n/a	chr4:97092391-97092402
21	CEBPB	chr4:97092245-97092570	HepG2	liver:	n/a	chr4:97092391-97092402
22	CEBPB	chr4:97196996-97197265	HepG2	liver:	n/a	chr4:97197086-97197097 chr4:97197086-97197099 chr4:97197088-97197099
23	CEBPB	chr4:97058408-97058689	HepG2	liver:	n/a	chr4:97058529-97058540 chr4:97058530-97058541
24	CEBPZ	chr4:97142345-97142434	HepG2	liver:	n/a	n/a
25	CHD2	chr4:97148728-97148991	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr4:97181136-97181419	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr4:97091420-97091570	HVMF	connective:	n/a	n/a
28	CTCF	chr4:97091460-97091610	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr4:97091440-97091590	GM12871	blood:	n/a	n/a
30	CTCF	chr4:97091408-97091630	MCF-7	breast:	n/a	n/a
31	CTCF	chr4:97091429-97091618	GM12892	blood:	n/a	n/a
32	CTCF	chr4:97091318-97091658	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr4:97149800-97149950	MCF-7	breast:	n/a	n/a
34	CTCF	chr4:97091400-97091550	GM12873	blood:	n/a	n/a
35	CTCF	chr4:97091500-97091650	GM12875	blood:	n/a	n/a
36	CTCF	chr4:97091580-97091730	GM12868	blood:	n/a	n/a
37	CTCF	chr4:97091420-97091570	GM12870	blood:	n/a	n/a
38	CTCF	chr4:97149860-97150010	HEK293	kidney:	n/a	n/a
39	CTCF	chr4:97091442-97091548	Fibrobl	skin:	n/a	n/a
40	CTCF	chr4:97091420-97091570	HCT-116	colon:	n/a	n/a
41	CTCF	chr4:97185140-97185290	K562	blood:	n/a	n/a
42	CTCF	chr4:97091440-97091590	HEK293	kidney:	n/a	n/a
43	CTCF	chr4:97091460-97091610	GM12872	blood:	n/a	n/a
44	CTCF	chr4:97149760-97149910	MCF-7	breast:	n/a	n/a
45	CTCF	chr4:97091485-97091553	GM10248	blood:	n/a	n/a
46	CTCF	chr4:97091500-97091650	BE2_C	brain:	n/a	n/a
47	CTCF	chr4:97100780-97100930	AG09319	gingival:	n/a	n/a
48	CTCF	chr4:97091440-97091590	BE2_C	brain:	n/a	n/a
49	CTCF	chr4:97091400-97091632	GM12891	blood:	n/a	n/a
50	CTCF	chr4:97091394-97091609	HepG2	liver:	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	chr4:97148730-97148780	U87	brain:	n/a
2	chr4:97182116-97182166	NB4	blood:	n/a
3	chr4:97148730-97148780	CMK	blood:	n/a
4	chr4:97047512-97047562	AG04449	skin:	fetal
5	chr4:97148730-97148780	SK-N-SH	brain:	n/a
6	chr4:97047135-97047185	HEK293	kidney:	embryo
7	chr4:97141368-97141418	SK-N-SH_RA	brain:	n/a
8	chr4:97047512-97047562	AoSMC	blood vessel:	n/a
9	chr4:97047512-97047562	HMEC	breast:	n/a
10	chr4:97047181-97047231	GM12878	blood:	n/a
11	chr4:97047135-97047185	NHDF-neo	bronchial:	n/a
12	chr4:97182116-97182166	HIPEpiC	eye:	n/a
13	chr4:97148730-97148780	HCM	heart:	n/a
14	chr4:97141368-97141418	HCPEpiC	choroid plexus:	n/a
15	chr4:97148730-97148780	Caco-2	colon:	n/a
16	chr4:97047135-97047185	HPAEpiC	pulmonary alveolar:	n/a
17	chr4:97148730-97148780	LNCaP	prostate:	n/a
18	chr4:97182116-97182166	AG10803	skin:	n/a
19	chr4:97047135-97047185	PrEC	prostate:	n/a
20	chr4:97047512-97047562	MCF10A-Er-Src	breast:	n/a
21	chr4:97141368-97141418	ProgFib	skin:	n/a
22	chr4:97047512-97047562	H1-hESC	embryonic stem cell:	embryo
23	chr4:97047181-97047231	BJ	skin:	n/a
24	chr4:97047135-97047185	LNCaP	prostate:	n/a
25	chr4:97182116-97182166	BJ	skin:	n/a
26	chr4:97148730-97148780	Hepatocyte	liver:	n/a
27	chr4:97047181-97047231	SK-N-MC	brain:	n/a
28	chr4:97182116-97182166	AG09319	gingival:	n/a
29	chr4:97148730-97148780	MCF-7	breast:	n/a
30	chr4:97182116-97182166	SK-N-SH_RA	brain:	n/a
31	chr4:97141368-97141418	SAEC	small airway:	n/a
32	chr4:97148730-97148780	HepG2	liver:	n/a
33	chr4:97047181-97047231	NH-A	brain:	n/a
34	chr4:97148730-97148780	HNPCEpiC	eye:	n/a
35	chr4:97182116-97182166	AG04449	skin:	fetal
36	chr4:97047135-97047185	AoSMC	blood vessel:	n/a
37	chr4:97182116-97182166	SAEC	small airway:	n/a
38	chr4:97047181-97047231	GM19239	blood:	n/a
39	chr4:97047512-97047562	HRCEpiC	kidney:	n/a
40	chr4:97047181-97047231	ovcar-3	ovarian:	n/a
41	chr4:97148730-97148780	BJ	skin:	n/a
42	chr4:97047181-97047231	GM12891	blood:	n/a
43	chr4:97047135-97047185	HCPEpiC	choroid plexus:	n/a
44	chr4:97141368-97141418	NHBE	bronchial:	n/a
45	chr4:97047135-97047185	NT2-D1	testis:	n/a
46	chr4:97047135-97047185	NB4	blood:	n/a
47	chr4:97141368-97141418	HEK293	kidney:	embryo
48	chr4:97141368-97141418	PrEC	prostate:	n/a
49	chr4:97047512-97047562	HAEpiC	amniotic membrane:	n/a
50	chr4:97047135-97047185	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:97091475..97092009-chr4:98641981..98642501,2	MCF-7	breast:
2	chr4:97080339..97083190-chr4:97083678..97085424,2	K562	blood:
3	chr4:97103707..97106316-chr4:97112297..97115167,2	K562	blood:
4	chr4:97098106..97100868-chr4:97101753..97104134,2	K562	blood:
5	chr4:97090980..97093234-chr4:97096848..97099424,2	K562	blood:
6	chr4:97075485..97077606-chr4:97078674..97081310,2	K562	blood:
7	chr4:97090980..97093234-chr4:97096848..97099424,2	K562	blood:
8	chr4:97080339..97083190-chr4:97083678..97085424,2	K562	blood:
9	chr4:97090606..97093234-chr4:97096848..97099825,3	K562	blood:
10	chr4:97204222..97205966-chr4:97206787..97209522,2	K562	blood:
11	chr4:97098106..97100868-chr4:97101753..97104134,2	K562	blood:
12	chr4:97090606..97093234-chr4:97096848..97099825,3	K562	blood:
13	chr4:97103707..97106316-chr4:97112297..97115167,2	K562	blood:
14	chr4:97174563..97176732-chr4:97282381..97284958,2	K562	blood:
15	chr4:97075485..97077606-chr4:97078674..97081310,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDHA2-3	chr4:97133430-97134251	NONHSAT097469

No data

Variant related genes	Relation type
ENSG00000250655	TF binding region
RNU6-34P	TF binding region
ENSG00000250655	CpG island
RNU6-34P	CpG island

Extended variants
information (count: 2399 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:2399 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559000356	chr4:97035403-97035404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs149865778	chr4:97035436-97035437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574043213	chr4:97035463-97035464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114226329	chr4:97035485-97035486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs147590852	chr4:97035531-97035532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs117946001	chr4:97035547-97035548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545190490	chr4:97035558-97035559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs7695694	chr4:97035575-97035576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs187344964	chr4:97035596-97035597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115861111	chr4:97035601-97035602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191737246	chr4:97035636-97035637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183994807	chr4:97035692-97035693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs551955265	chr4:97035694-97035695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs530052142	chr4:97035701-97035702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142116664	chr4:97035705-97035706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563496043	chr4:97035753-97035754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532298600	chr4:97035755-97035756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs17025073	chr4:97035768-97035769	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs565810745	chr4:97035787-97035788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534418011	chr4:97035792-97035793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534396056	chr4:97035829-97035830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548194251	chr4:97035864-97035865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555833247	chr4:97035885-97035886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188290442	chr4:97035936-97035937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs536560906	chr4:97035938-97035939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs180754795	chr4:97035948-97035949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs576231772	chr4:97035952-97035953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539182047	chr4:97035967-97035968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185613058	chr4:97035987-97035988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs190567489	chr4:97035994-97035995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs181841807	chr4:97036023-97036024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs555019973	chr4:97036050-97036051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs574857319	chr4:97036125-97036126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs543743030	chr4:97036128-97036129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs375580006	chr4:97036173-97036174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs565110703	chr4:97041209-97041210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs116336486	chr4:97041213-97041214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs184527072	chr4:97041232-97041233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs374453856	chr4:97041239-97041240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561088509	chr4:97041266-97041267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs529867664	chr4:97041276-97041277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs549991930	chr4:97041295-97041296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs571886438	chr4:97041299-97041300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532088142	chr4:97041311-97041312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs141263384	chr4:97041343-97041344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189024377	chr4:97041355-97041356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs569285503	chr4:97041360-97041361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs76252711	chr4:97041378-97041379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77170893	chr4:97041382-97041383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs567531021	chr4:97041392-97041393	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	19197363	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20688739	CNVD

Chromatin state (count:158 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:97035400-97035800	Enhancers	Fetal Brain Male	brain
2	chr4:97035800-97036200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr4:97041200-97041800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr4:97041600-97042600	Enhancers	HSMMtube	muscle
5	chr4:97052200-97052600	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr4:97066400-97068000	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr4:97066400-97068200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr4:97066400-97068200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr4:97066600-97067400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr4:97066800-97067200	Enhancers	Osteobl	bone
11	chr4:97066800-97067400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr4:97067400-97067800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr4:97067800-97068400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr4:97068200-97071000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr4:97068200-97071000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr4:97070800-97071200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr4:97071000-97071200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr4:97071000-97071600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr4:97071000-97071600	Active TSS	Right Atrium	heart
20	chr4:97071200-97071400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:97071200-97071400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr4:97071200-97071400	Enhancers	HSMM	muscle
23	chr4:97071200-97071600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr4:97071600-97071800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr4:97075200-97076600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr4:97075800-97076400	Enhancers	Muscle Satellite Cultured Cells	--
27	chr4:97075800-97076400	Enhancers	Osteobl	bone
28	chr4:97076000-97076400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr4:97076000-97076400	Enhancers	NH-A	brain
30	chr4:97076000-97076800	Enhancers	HSMM	muscle
31	chr4:97079600-97080000	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr4:97080000-97083600	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr4:97083400-97083800	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr4:97083600-97084000	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr4:97083600-97084000	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr4:97083600-97084200	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr4:97083600-97085200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr4:97083600-97085200	Enhancers	Muscle Satellite Cultured Cells	--
39	chr4:97083600-97088200	Enhancers	Osteobl	bone
40	chr4:97083800-97084200	Enhancers	HSMMtube	muscle
41	chr4:97084200-97084600	Weak transcription	HSMMtube	muscle
42	chr4:97084600-97085200	Enhancers	HSMMtube	muscle
43	chr4:97084800-97085200	Enhancers	HSMM	muscle
44	chr4:97085000-97085600	Enhancers	NHDF-Ad	bronchial
45	chr4:97085000-97086200	Enhancers	NH-A	brain
46	chr4:97085200-97085400	Flanking Active TSS	HSMMtube	muscle
47	chr4:97085200-97085800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr4:97085200-97085800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
49	chr4:97085200-97085800	Genic enhancers	HSMM	muscle
50	chr4:97085200-97087000	Enhancers	HMEC	breast

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