Variant report

Variant	nsv582521
Chromosome Location	chr2:99847890-99922967
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	ARID3A	chr2:99895164-99895764	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:99870939-99870988	K562	blood:	n/a	n/a
3	BATF	chr2:99856950-99857204	GM12878	blood:	n/a	n/a
4	BATF	chr2:99856972-99857225	GM12878	blood:	n/a	n/a
5	BHLHE40	chr2:99895235-99895694	HepG2	liver:	n/a	n/a
6	BHLHE40	chr2:99854703-99854753	K562	blood:	n/a	n/a
7	BHLHE40	chr2:99856952-99857274	GM12878	blood:	n/a	n/a
8	BRCA1	chr2:99897017-99897190	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr2:99887235-99887673	K562	blood:	n/a	n/a
10	CBX3	chr2:99887282-99887749	K562	blood:	n/a	n/a
11	CEBPB	chr2:99896815-99897096	A549	lung:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
12	CEBPB	chr2:99895163-99895672	MCF-7	breast:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
13	CEBPB	chr2:99867010-99867376	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr2:99895245-99895503	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
15	CEBPB	chr2:99867010-99867383	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:99867003-99867374	HepG2	liver:	n/a	n/a
17	CEBPB	chr2:99873103-99873596	ECC-1	luminal epithelium:	n/a	n/a
18	CEBPB	chr2:99895160-99895686	IMR90	lung:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
19	CEBPB	chr2:99867094-99867402	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr2:99895140-99895648	MCF-7	breast:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
21	CEBPB	chr2:99895106-99895826	Hela-S3	cervix:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
22	CEBPB	chr2:99895309-99895544	K562	blood:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
23	CEBPB	chr2:99896754-99897198	Hela-S3	cervix:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
24	CEBPB	chr2:99895111-99895596	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
25	CEBPB	chr2:99898969-99899023	K562	blood:	n/a	n/a
26	CEBPB	chr2:99867071-99867369	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr2:99896759-99897060	MCF-7	breast:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
28	CEBPB	chr2:99895144-99895666	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
29	CEBPB	chr2:99896793-99897128	HepG2	liver:	n/a	chr2:99896933-99896944 chr2:99896995-99897012
30	CEBPB	chr2:99895210-99895580	A549	lung:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
31	CEBPB	chr2:99895136-99895626	HepG2	liver:	n/a	chr2:99895401-99895414 chr2:99895403-99895414 chr2:99895401-99895412 chr2:99895401-99895414
32	CEBPB	chr2:99898960-99899066	HepG2	liver:	n/a	n/a
33	CHD2	chr2:99895156-99895749	Hela-S3	cervix:	n/a	n/a
34	CREB1	chr2:99867108-99867416	HepG2	liver:	n/a	n/a
35	CTCF	chr2:99862540-99862690	RPTEC	kidney:	n/a	n/a
36	CTCF	chr2:99862129-99862414	HepG2	liver:	n/a	n/a
37	CTCF	chr2:99862580-99862730	SAEC	small airway:	n/a	n/a
38	CTCF	chr2:99855805-99856036	K562	blood:	n/a	n/a
39	CTCF	chr2:99855800-99855950	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr2:99855880-99856030	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr2:99855840-99855990	HPF	lung:	n/a	n/a
42	CTCF	chr2:99862183-99862352	HepG2	liver:	n/a	n/a
43	CTCF	chr2:99862606-99862682	NHEK	skin:	n/a	n/a
44	CTCF	chr2:99862236-99862352	MCF-7	breast:	n/a	n/a
45	CTCF	chr2:99855880-99856030	GM12870	blood:	n/a	n/a
46	CTCF	chr2:99862600-99862750	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr2:99855940-99856090	SAEC	small airway:	n/a	n/a
48	CTCF	chr2:99869093-99869142	GM12878	blood:	n/a	n/a
49	CTCF	chr2:99855820-99855970	HVMF	connective:	n/a	n/a
50	CTCF	chr2:99862580-99862730	HL-60	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:99918664-99918714	GM12892	blood:	n/a
2	chr2:99918664-99918714	GM12892	blood:	n/a
3	chr2:99871270-99871320	HPAEpiC	pulmonary alveolar:	n/a
4	chr2:99871575-99871625	HCPEpiC	choroid plexus:	n/a
5	chr2:99871575-99871625	BE2_C	brain:	n/a
6	chr2:99912152-99912202	ProgFib	skin:	n/a
7	chr2:99871575-99871625	HL-60	blood:	n/a
8	chr2:99858763-99858813	SK-N-SH_RA	brain:	n/a
9	chr2:99867344-99867394	HCM	heart:	n/a
10	chr2:99871988-99872038	GM12891	blood:	n/a
11	chr2:99858763-99858813	NH-A	brain:	n/a
12	chr2:99908962-99909012	A549	lung:	n/a
13	chr2:99871988-99872038	HPAEpiC	pulmonary alveolar:	n/a
14	chr2:99918767-99918817	LNCaP	prostate:	n/a
15	chr2:99918767-99918817	Jurkat	blood:	n/a
16	chr2:99918664-99918714	HRPEpiC	eye:	n/a
17	chr2:99872119-99872169	HCPEpiC	choroid plexus:	n/a
18	chr2:99918603-99918653	AG10803	skin:	n/a
19	chr2:99918042-99918092	GM12891	blood:	n/a
20	chr2:99871988-99872038	AG10803	skin:	n/a
21	chr2:99918767-99918817	IMR90	lung:	fetal
22	chr2:99871738-99871788	HAEpiC	amniotic membrane:	n/a
23	chr2:99908962-99909012	NB4	blood:	n/a
24	chr2:99871270-99871320	GM19239	blood:	n/a
25	chr2:99918603-99918653	GM06990	blood:	n/a
26	chr2:99908962-99909012	HPAEpiC	pulmonary alveolar:	n/a
27	chr2:99918767-99918817	ECC-1	luminal epithelium:	n/a
28	chr2:99912152-99912202	U87	brain:	n/a
29	chr2:99912152-99912202	IMR90	lung:	fetal
30	chr2:99871270-99871320	IMR90	lung:	fetal
31	chr2:99871988-99872038	GM06990	blood:	n/a
32	chr2:99908962-99909012	SAEC	small airway:	n/a
33	chr2:99871270-99871320	A549	lung:	n/a
34	chr2:99918042-99918092	SK-N-SH	brain:	n/a
35	chr2:99871575-99871625	HRPEpiC	eye:	n/a
36	chr2:99912152-99912202	Jurkat	blood:	n/a
37	chr2:99871988-99872038	HepG2	liver:	n/a
38	chr2:99871738-99871788	SKMC	muscle:	n/a
39	chr2:99867344-99867394	AG04450	lung:	fetal
40	chr2:99867344-99867394	SK-N-SH_RA	brain:	n/a
41	chr2:99871575-99871625	AG10803	skin:	n/a
42	chr2:99871738-99871788	PFSK-1	brain:	n/a
43	chr2:99917669-99917719	Caco-2	colon:	n/a
44	chr2:99871988-99872038	AG04449	skin:	fetal
45	chr2:99871988-99872038	IMR90	lung:	fetal
46	chr2:99871988-99872038	AoSMC	blood vessel:	n/a
47	chr2:99912152-99912202	NHDF-neo	bronchial:	n/a
48	chr2:99918042-99918092	NT2-D1	testis:	n/a
49	chr2:99918767-99918817	SK-N-SH	brain:	n/a
50	chr2:99872119-99872169	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:99795164..99797878-chr2:99854234..99856098,2	K562	blood:
2	chr2:99906899..99908404-chr2:99910442..99912055,2	K562	blood:
3	chr2:99895187..99896703-chr2:99951053..99953668,2	MCF-7	breast:
4	chr2:99861336..99864136-chr2:99868070..99870464,2	K562	blood:
5	chr2:99860434..99863311-chr2:99975532..99977093,2	MCF-7	breast:
6	chr2:99906899..99908404-chr2:99910442..99912055,2	K562	blood:
7	chr2:99866201..99868659-chr2:99869387..99872001,2	K562	blood:
8	chr2:99919697..99922118-chr2:99951528..99953553,2	K562	blood:
9	chr2:99853855..99856752-chr2:99861068..99863308,2	K562	blood:
10	chr2:99900352..99903264-chr2:99910186..99913049,2	K562	blood:
11	chr2:99905599..99909122-chr2:99945751..99948599,3	MCF-7	breast:
12	chr2:99853855..99856752-chr2:99861068..99863308,2	K562	blood:
13	chr2:99862632..99864910-chr2:99865655..99867519,2	K562	blood:
14	chr2:99862632..99864910-chr2:99865655..99867519,2	K562	blood:
15	chr2:99918821..99920555-chr2:99920714..99922754,2	MCF-7	breast:
16	chr2:99900352..99903264-chr2:99910186..99913049,2	K562	blood:
17	chr2:99855888..99858243-chr2:99952048..99955134,3	MCF-7	breast:
18	chr2:99771253..99773056-chr2:99921350..99922897,2	K562	blood:
19	chr2:99861336..99864136-chr2:99868070..99870464,2	K562	blood:

Variant related genes	Relation type
C2orf15	TF binding region
LYG1	TF binding region
LYG2	TF binding region
C2orf15	CpG island
LYG1	CpG island
LYG2	CpG island
ENSG00000135951	chromatin interactions
ENSG00000241962	chromatin interactions
ENSG00000273155	chromatin interactions
ENSG00000144214	chromatin interactions
ENSG00000158417	chromatin interactions
ENSG00000185674	chromatin interactions
ENSG00000115514	chromatin interactions
ENSG00000158411	chromatin interactions
ENSG00000185414	chromatin interactions
ENSG00000144182	chromatin interactions

Extended variants
information (count: 2604 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2604 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7603462	chr2:99847890-99847891	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs78936118	chr2:99847894-99847895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148699847	chr2:99847898-99847899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551845995	chr2:99847899-99847900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571662215	chr2:99847905-99847906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376493997	chr2:99847946-99847947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551640445	chr2:99847985-99847986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs180849558	chr2:99847987-99847988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531089074	chr2:99848057-99848058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186456781	chr2:99848085-99848086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs199519776	chr2:99848214-99848215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190837180	chr2:99848215-99848216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs79648154	chr2:99848239-99848240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372708996	chr2:99848280-99848281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553731830	chr2:99848352-99848353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183106937	chr2:99848454-99848455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538263863	chr2:99848474-99848475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs558574975	chr2:99848486-99848487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs144535918	chr2:99848492-99848493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544360192	chr2:99848635-99848636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569896758	chr2:99848662-99848663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554324950	chr2:99848704-99848705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574317922	chr2:99848778-99848779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540131454	chr2:99848790-99848791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185957867	chr2:99848864-99848865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs13031919	chr2:99848932-99848933	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs377330084	chr2:99848947-99848948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545078851	chr2:99848957-99848958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369597598	chr2:99848987-99848988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112842287	chr2:99848993-99848994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530926996	chr2:99849045-99849046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs114558957	chr2:99849090-99849091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567839351	chr2:99849152-99849153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs76060792	chr2:99849184-99849185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs77889585	chr2:99849256-99849257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530366137	chr2:99849275-99849276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547305610	chr2:99849304-99849305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376553637	chr2:99849324-99849325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12993310	chr2:99849336-99849337	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs183113591	chr2:99849381-99849382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554029646	chr2:99849387-99849388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538600496	chr2:99849429-99849430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114600709	chr2:99849431-99849432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188254321	chr2:99849434-99849435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537520171	chr2:99849484-99849485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571625202	chr2:99849594-99849595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs6719145	chr2:99849617-99849618	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs574281755	chr2:99849698-99849699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533749136	chr2:99849748-99849749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs6748497	chr2:99849762-99849763	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:476 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:99818200-99854600	Weak transcription	Left Ventricle	heart
2	chr2:99840800-99874400	Weak transcription	Aorta	Aorta
3	chr2:99853600-99863200	Weak transcription	Esophagus	oesophagus
4	chr2:99854600-99854800	Enhancers	Left Ventricle	heart
5	chr2:99854600-99855200	Enhancers	K562	blood
6	chr2:99854800-99865800	Weak transcription	Left Ventricle	heart
7	chr2:99855200-99855600	Flanking Active TSS	K562	blood
8	chr2:99855600-99855800	Enhancers	K562	blood
9	chr2:99858200-99859200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr2:99858400-99859200	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr2:99858800-99864800	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr2:99860400-99899800	Weak transcription	Psoas Muscle	Psoas
13	chr2:99860800-99864400	Weak transcription	Lung	lung
14	chr2:99861200-99879200	Weak transcription	Stomach Smooth Muscle	stomach
15	chr2:99861200-99900800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr2:99861800-99871200	Weak transcription	Colon Smooth Muscle	Colon
17	chr2:99861800-99899400	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr2:99862000-99863600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr2:99862000-99879200	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr2:99862200-99864200	Enhancers	HepG2	liver
21	chr2:99862600-99863200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr2:99863000-99863400	Enhancers	Gastric	stomach
23	chr2:99863200-99863400	ZNF genes & repeats	Esophagus	oesophagus
24	chr2:99864200-99867200	Weak transcription	HepG2	liver
25	chr2:99867200-99867400	Enhancers	HepG2	liver
26	chr2:99867200-99867600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr2:99869800-99880000	Weak transcription	Right Ventricle	heart
28	chr2:99870600-99871200	Enhancers	Stomach Mucosa	stomach
29	chr2:99872000-99872200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr2:99872000-99873200	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr2:99872000-99873800	Enhancers	HMEC	breast
32	chr2:99872200-99872400	Bivalent Enhancer	HepG2	liver
33	chr2:99872200-99872600	Enhancers	NHEK	skin
34	chr2:99872200-99872800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr2:99872200-99873000	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr2:99872200-99873600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr2:99872400-99872800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr2:99872400-99873000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr2:99872400-99873000	Enhancers	Esophagus	oesophagus
40	chr2:99872400-99873200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr2:99872400-99873600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr2:99872600-99873000	Flanking Active TSS	NHEK	skin
43	chr2:99872600-99873200	Enhancers	NH-A	brain
44	chr2:99872800-99873200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr2:99872800-99873400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr2:99873000-99873800	Enhancers	NHEK	skin
47	chr2:99873000-99877600	Weak transcription	Esophagus	oesophagus
48	chr2:99873200-99875600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr2:99873400-99877600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr2:99873600-99877800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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