Variant report

Variant	nsv961450
Chromosome Location	chr2:96082078-96152892
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	BATF	chr2:96086663-96086898	GM12878	blood:	n/a	n/a
2	BHLHE40	chr2:96095542-96095812	HepG2	liver:	n/a	n/a
3	CBX3	chr2:96086613-96087007	K562	blood:	n/a	n/a
4	CEBPB	chr2:96082659-96082868	HepG2	liver:	n/a	chr2:96082835-96082848 chr2:96082836-96082847 chr2:96082835-96082848 chr2:96082835-96082848
5	CEBPB	chr2:96086532-96086791	IMR90	lung:	n/a	n/a
6	CEBPB	chr2:96086158-96086233	HepG2	liver:	n/a	n/a
7	CEBPB	chr2:96086584-96086784	A549	lung:	n/a	n/a
8	CEBPB	chr2:96082668-96082929	A549	lung:	n/a	chr2:96082835-96082848 chr2:96082836-96082847 chr2:96082835-96082848 chr2:96082835-96082848
9	CEBPB	chr2:96100508-96100752	IMR90	lung:	n/a	n/a
10	CEBPB	chr2:96082826-96082851	K562	blood:	n/a	chr2:96082835-96082848 chr2:96082836-96082847 chr2:96082835-96082848 chr2:96082835-96082848
11	CEBPB	chr2:96086461-96086787	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:96086087-96086333	K562	blood:	n/a	n/a
13	CEBPB	chr2:96082817-96082928	H1-hESC	embryonic stem cell:	n/a	chr2:96082835-96082848 chr2:96082836-96082847 chr2:96082835-96082848 chr2:96082835-96082848
14	CEBPB	chr2:96086043-96086325	K562	blood:	n/a	n/a
15	CTCF	chr2:96146779-96146846	GM10248	blood:	n/a	n/a
16	CTCF	chr2:96105438-96105486	GM13976	blood:	n/a	n/a
17	CTCF	chr2:96129197-96129343	MCF-7	breast:	n/a	chr2:96129299-96129317
18	CTCF	chr2:96086630-96086688	K562	blood:	n/a	n/a
19	CTCF	chr2:96088577-96088647	GM13976	blood:	n/a	n/a
20	CTCF	chr2:96135332-96135366	GM10266	blood:	n/a	n/a
21	CTCF	chr2:96086698-96086990	LNCaP	prostate:	n/a	chr2:96086824-96086833 chr2:96086823-96086836 chr2:96086818-96086836 chr2:96086813-96086834
22	CTCF	chr2:96095932-96096026	LNCaP	prostate:	n/a	n/a
23	CTCF	chr2:96086714-96086901	GM19239	blood:	n/a	chr2:96086824-96086833 chr2:96086823-96086836 chr2:96086818-96086836 chr2:96086813-96086834
24	CTCF	chr2:96086520-96086670	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr2:96095715-96095778	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr2:96086500-96086650	GM12873	blood:	n/a	n/a
27	CTCF	chr2:96086500-96086650	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr2:96092506-96092572	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr2:96086520-96086670	NHDF-neo	bronchial:	n/a	n/a
30	CTCF	chr2:96148072-96148126	Medullo	brain:	n/a	n/a
31	CTCF	chr2:96129238-96129338	GM20000	blood:	n/a	chr2:96129299-96129317
32	CTCF	chr2:96086520-96086670	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr2:96086702-96086971	Gliobla	brain:	n/a	chr2:96086824-96086833 chr2:96086823-96086836 chr2:96086818-96086836 chr2:96086813-96086834
34	CTCF	chr2:96129255-96129343	HUVEC	blood vessel:	n/a	chr2:96129299-96129317
35	CTCF	chr2:96129245-96129272	GM19239	blood:	n/a	n/a
36	CTCF	chr2:96086520-96086670	HFF	foreskin:	n/a	n/a
37	CTCF	chr2:96111409-96111438	GM13976	blood:	n/a	n/a
38	CTCF	chr2:96085004-96085080	LNCaP	prostate:	n/a	n/a
39	CTCF	chr2:96086520-96086670	AG09319	gingival:	n/a	n/a
40	CTCF	chr2:96086500-96086650	BJ	skin:	n/a	n/a
41	CTCF	chr2:96086708-96086931	GM12892	blood:	n/a	chr2:96086824-96086833 chr2:96086823-96086836 chr2:96086818-96086836 chr2:96086813-96086834
42	CTCF	chr2:96101649-96101794	NHEK	skin:	n/a	n/a
43	CTCF	chr2:96129169-96129366	MCF-7	breast:	n/a	chr2:96129299-96129317
44	CTCF	chr2:96086715-96086927	GM19240	blood:	n/a	chr2:96086824-96086833 chr2:96086823-96086836 chr2:96086818-96086836 chr2:96086813-96086834
45	CTCF	chr2:96129110-96129475	A549	lung:	n/a	chr2:96129299-96129317
46	CTCF	chr2:96086720-96086945	GM13976	blood:	n/a	chr2:96086824-96086833 chr2:96086823-96086836 chr2:96086818-96086836 chr2:96086813-96086834
47	CTCF	chr2:96086520-96086670	RPTEC	kidney:	n/a	n/a
48	CTCF	chr2:96086713-96086902	GM12891	blood:	n/a	chr2:96086824-96086833 chr2:96086823-96086836 chr2:96086818-96086836 chr2:96086813-96086834
49	CTCF	chr2:96086721-96086897	Hela-S3	cervix:	n/a	chr2:96086824-96086833 chr2:96086823-96086836 chr2:96086818-96086836 chr2:96086813-96086834
50	CTCF	chr2:96086712-96086900	MCF-7	breast:	n/a	chr2:96086824-96086833 chr2:96086823-96086836 chr2:96086818-96086836 chr2:96086813-96086834

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:96093031-96093081	Caco-2	colon:	n/a
2	chr2:96148075-96148125	SKMC	muscle:	n/a
3	chr2:96149768-96149818	Caco-2	colon:	n/a
4	chr2:96093031-96093081	Hela-S3	cervix:	n/a
5	chr2:96148075-96148125	ECC-1	luminal epithelium:	n/a
6	chr2:96093020-96093070	GM06990	blood:	n/a
7	chr2:96151359-96151409	SK-N-MC	brain:	n/a
8	chr2:96093020-96093070	ProgFib	skin:	n/a
9	chr2:96097880-96097930	HMEC	breast:	n/a
10	chr2:96151359-96151409	HEK293	kidney:	embryo
11	chr2:96093020-96093070	HL-60	blood:	n/a
12	chr2:96149768-96149818	AG09309	skin:	n/a
13	chr2:96151359-96151409	NT2-D1	testis:	n/a
14	chr2:96151359-96151409	SK-N-SH_RA	brain:	n/a
15	chr2:96097880-96097930	K562	blood:	n/a
16	chr2:96093020-96093070	HIPEpiC	eye:	n/a
17	chr2:96149768-96149818	T-47D	breast:	n/a
18	chr2:96148075-96148125	HCT-116	colon:	n/a
19	chr2:96151359-96151409	NH-A	brain:	n/a
20	chr2:96149768-96149818	SAEC	small airway:	n/a
21	chr2:96151370-96151420	AoSMC	blood vessel:	n/a
22	chr2:96151370-96151420	AG09309	skin:	n/a
23	chr2:96151359-96151409	HAEpiC	amniotic membrane:	n/a
24	chr2:96093031-96093081	HepG2	liver:	n/a
25	chr2:96093031-96093081	LNCaP	prostate:	n/a
26	chr2:96151370-96151420	ProgFib	skin:	n/a
27	chr2:96151370-96151420	Hepatocyte	liver:	n/a
28	chr2:96093031-96093081	AG09319	gingival:	n/a
29	chr2:96093020-96093070	AG09319	gingival:	n/a
30	chr2:96151359-96151409	SKMC	muscle:	n/a
31	chr2:96093020-96093070	SK-N-SH	brain:	n/a
32	chr2:96093020-96093070	IMR90	lung:	fetal
33	chr2:96093020-96093070	GM12891	blood:	n/a
34	chr2:96097880-96097930	AG09309	skin:	n/a
35	chr2:96097880-96097930	BE2_C	brain:	n/a
36	chr2:96149768-96149818	NHDF-neo	bronchial:	n/a
37	chr2:96093031-96093081	NH-A	brain:	n/a
38	chr2:96093031-96093081	T-47D	breast:	n/a
39	chr2:96097880-96097930	LNCaP	prostate:	n/a
40	chr2:96093031-96093081	HCF	heart:	n/a
41	chr2:96093020-96093070	GM19239	blood:	n/a
42	chr2:96148075-96148125	Hela-S3	cervix:	n/a
43	chr2:96151359-96151409	U87	brain:	n/a
44	chr2:96093020-96093070	LNCaP	prostate:	n/a
45	chr2:96093031-96093081	AG09309	skin:	n/a
46	chr2:96151370-96151420	NT2-D1	testis:	n/a
47	chr2:96093020-96093070	BJ	skin:	n/a
48	chr2:96151370-96151420	HRCEpiC	kidney:	n/a
49	chr2:96148075-96148125	K562	blood:	n/a
50	chr2:96151370-96151420	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:96075502..96078062-chr2:96080565..96082450,2	K562	blood:
2	chr2:96065770..96068557-chr2:96149024..96150845,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNIP3-4	chr2:96080756-96082345	NONHSAT072486
2	lnc-FAHD2A-2	chr2:96100507-96100861	NONHSAT072487
3	lnc-FAHD2A-3	chr2:96101881-96102304	NONHSAT072488
4	lnc-ZNF514-8	chr2:96135337-96135526	NONHSAT072489
5	lnc-ZNF514-9	chr2:96152228-96152510	NONHSAT072490
6	lnc-ZNF514-8	chr2:96134611-96134638	NONHSAT072489

Variant related genes	Relation type
ENSG00000238162	TF binding region
TRIM43B	TF binding region
ENSG00000227120	TF binding region
UBTFL5	TF binding region
ENSG00000234903	TF binding region
ENSG00000233275	TF binding region
ENSG00000248821	TF binding region
ENSG00000238162	CpG island
TRIM43B	CpG island
ENSG00000227120	CpG island
UBTFL5	CpG island
ENSG00000234903	CpG island
ENSG00000233275	CpG island
ENSG00000248821	CpG island
ENSG00000115042	chromatin interactions

Extended variants
information (count: 291 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:291 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35655198	chr2:96082088-96082089	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs13015296	chr2:96082102-96082103	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs12995499	chr2:96082107-96082108	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs561194646	chr2:96082158-96082159	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs184707202	chr2:96082274-96082275	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs142968238	chr2:96082275-96082276	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs372347687	chr2:96082288-96082289	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs141593973	chr2:96082373-96082374	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs199748175	chr2:96082420-96082421	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs571354927	chr2:96082458-96082459	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs537189683	chr2:96082459-96082460	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs539572053	chr2:96082484-96082485	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs188451604	chr2:96082544-96082545	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs192229497	chr2:96082609-96082610	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs552964525	chr2:96082619-96082620	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs184612851	chr2:96082713-96082714	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs112709571	chr2:96082720-96082721	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs189359643	chr2:96082765-96082766	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs138414475	chr2:96082844-96082845	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs575334302	chr2:96082897-96082898	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs181936584	chr2:96082947-96082948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184379883	chr2:96083013-96083014	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs574906389	chr2:96083020-96083021	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs540847578	chr2:96083024-96083025	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs189039349	chr2:96083026-96083027	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs532878446	chr2:96083048-96083049	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs3967705	chr2:96083058-96083059	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs551392108	chr2:96083072-96083073	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs564821738	chr2:96083087-96083088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530528668	chr2:96083136-96083137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113218313	chr2:96083138-96083139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550660630	chr2:96083147-96083148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567378881	chr2:96083189-96083190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536037918	chr2:96083200-96083201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs546807990	chr2:96083202-96083203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200645037	chr2:96083211-96083212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2551307	chr2:96083215-96083216	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs149232023	chr2:96083273-96083274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558433646	chr2:96083284-96083285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575197280	chr2:96083309-96083310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537868871	chr2:96083413-96083414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554619594	chr2:96083429-96083430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs574907797	chr2:96083430-96083431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537061470	chr2:96083437-96083438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182194370	chr2:96083441-96083442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186275723	chr2:96083459-96083460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs377236303	chr2:96083511-96083512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs71427030	chr2:96083534-96083535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577369142	chr2:96083548-96083549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546478468	chr2:96083549-96083550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

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
Neuroblastoma	18574593	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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Breast cancer	22522925	CNVD
Epilepsy	22083797	CNVD

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:96070000-96083000	Weak transcription	Right Atrium	heart
2	chr2:96074600-96082600	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr2:96077600-96084800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr2:96079000-96082200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr2:96079600-96082200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr2:96079600-96084000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:96079800-96083000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr2:96080200-96082800	Weak transcription	Fetal Stomach	stomach
9	chr2:96080600-96082200	Weak transcription	Fetal Intestine Small	intestine
10	chr2:96084000-96084200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr2:96084800-96085000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr2:96085600-96085800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr2:96092800-96093000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
14	chr2:96098400-96098800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr2:96098400-96098800	Enhancers	Stomach Smooth Muscle	stomach
16	chr2:96098600-96098800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr2:96098600-96098800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr2:96098600-96098800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr2:96098600-96098800	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr2:96098600-96098800	Enhancers	HMEC	breast
21	chr2:96098600-96098800	Enhancers	HSMM	muscle
22	chr2:96098600-96098800	Enhancers	NHDF-Ad	bronchial
23	chr2:96098600-96099200	Enhancers	Osteobl	bone
24	chr2:96098600-96100800	Enhancers	Muscle Satellite Cultured Cells	--
25	chr2:96098800-96099200	Enhancers	NH-A	brain
26	chr2:96098800-96099800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr2:96098800-96099800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr2:96098800-96099800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr2:96098800-96099800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr2:96098800-96099800	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr2:96098800-96099800	Weak transcription	Stomach Smooth Muscle	stomach
32	chr2:96098800-96099800	Weak transcription	HMEC	breast
33	chr2:96098800-96099800	Weak transcription	HSMM	muscle
34	chr2:96098800-96099800	Weak transcription	NHDF-Ad	bronchial
35	chr2:96099200-96099600	Weak transcription	NH-A	brain
36	chr2:96099200-96099600	Weak transcription	Osteobl	bone
37	chr2:96099400-96100800	Enhancers	NHEK	skin
38	chr2:96099600-96100800	Enhancers	NH-A	brain
39	chr2:96099600-96100800	Enhancers	Osteobl	bone
40	chr2:96099800-96100000	Enhancers	Stomach Smooth Muscle	stomach
41	chr2:96099800-96100200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr2:96099800-96100200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr2:96099800-96100200	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr2:96099800-96100200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr2:96099800-96100200	Enhancers	Brain Anterior Caudate	brain
46	chr2:96099800-96100200	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr2:96099800-96100200	Enhancers	Fetal Heart	heart
48	chr2:96099800-96100200	Enhancers	Fetal Muscle Leg	muscle
49	chr2:96099800-96100200	Enhancers	Placenta	Placenta
50	chr2:96099800-96100200	Enhancers	Lung	lung

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