Variant report

Variant	nsv874850
Chromosome Location	chr2:112052955-112163931
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:746)
CpG islands
(count:122)
Chromatin interactive
region (count:3)
LncRNA
region (count:33)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:746 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:112077982-112078035	K562	blood:	n/a	n/a
2	ARID3A	chr2:112142989-112143245	K562	blood:	n/a	n/a
3	ARID3A	chr2:112134733-112134923	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:112078700-112078866	K562	blood:	n/a	n/a
5	ATF1	chr2:112139588-112139732	K562	blood:	n/a	n/a
6	ATF1	chr2:112123600-112123901	K562	blood:	n/a	n/a
7	ATF1	chr2:112104247-112104437	K562	blood:	n/a	n/a
8	BACH1	chr2:112078561-112079019	H1-hESC	embryonic stem cell:	n/a	chr2:112078792-112078806
9	BACH1	chr2:112078641-112078944	K562	blood:	n/a	chr2:112078792-112078806
10	BACH1	chr2:112143146-112143417	K562	blood:	n/a	n/a
11	BATF	chr2:112131695-112131857	GM12878	blood:	n/a	n/a
12	BATF	chr2:112077128-112077551	GM12878	blood:	n/a	n/a
13	BATF	chr2:112072875-112073150	GM12878	blood:	n/a	chr2:112073011-112073022 chr2:112072925-112072935
14	BATF	chr2:112077193-112077517	GM12878	blood:	n/a	n/a
15	BATF	chr2:112073963-112074275	GM12878	blood:	n/a	n/a
16	BATF	chr2:112125609-112126213	GM12878	blood:	n/a	chr2:112125629-112125642
17	BATF	chr2:112158868-112159229	GM12878	blood:	n/a	chr2:112159209-112159219
18	BATF	chr2:112072847-112073098	GM12878	blood:	n/a	chr2:112073011-112073022 chr2:112072925-112072935
19	BATF	chr2:112158949-112159184	GM12878	blood:	n/a	n/a
20	BATF	chr2:112125762-112126285	GM12878	blood:	n/a	n/a
21	BATF	chr2:112074635-112074933	GM12878	blood:	n/a	chr2:112074773-112074784
22	BATF	chr2:112074557-112074916	GM12878	blood:	n/a	chr2:112074773-112074784
23	BCL11A	chr2:112087560-112087812	GM12878	blood:	n/a	n/a
24	BCL11A	chr2:112072754-112073092	GM12878	blood:	n/a	chr2:112072837-112072846
25	BCL11A	chr2:112125764-112126223	GM12878	blood:	n/a	n/a
26	BCL11A	chr2:112072806-112073106	GM12878	blood:	n/a	chr2:112072837-112072846
27	BCL11A	chr2:112125918-112126134	GM12878	blood:	n/a	n/a
28	BHLHE40	chr2:112078723-112078845	K562	blood:	n/a	n/a
29	BHLHE40	chr2:112133109-112133309	K562	blood:	n/a	n/a
30	CBX3	chr2:112158181-112158517	K562	blood:	n/a	n/a
31	CBX3	chr2:112097533-112097824	K562	blood:	n/a	n/a
32	CBX3	chr2:112105200-112105741	K562	blood:	n/a	n/a
33	CBX3	chr2:112104099-112104804	K562	blood:	n/a	n/a
34	CBX3	chr2:112116534-112117202	K562	blood:	n/a	n/a
35	CBX3	chr2:112078409-112078978	K562	blood:	n/a	n/a
36	CBX3	chr2:112109995-112110254	K562	blood:	n/a	n/a
37	CBX3	chr2:112116542-112117069	K562	blood:	n/a	n/a
38	CBX3	chr2:112139460-112139855	K562	blood:	n/a	n/a
39	CBX3	chr2:112123477-112124140	K562	blood:	n/a	n/a
40	CBX3	chr2:112077663-112078252	K562	blood:	n/a	n/a
41	CBX3	chr2:112117660-112118021	K562	blood:	n/a	n/a
42	CBX3	chr2:112109931-112110500	K562	blood:	n/a	n/a
43	CBX3	chr2:112097460-112097828	K562	blood:	n/a	n/a
44	CEBPB	chr2:112125562-112125759	IMR90	lung:	n/a	n/a
45	CEBPB	chr2:112132889-112133427	K562	blood:	n/a	chr2:112133186-112133195 chr2:112133185-112133196 chr2:112133184-112133197 chr2:112133186-112133195 chr2:112133184-112133197 chr2:112133186-112133195
46	CEBPB	chr2:112133123-112133338	A549	lung:	n/a	chr2:112133186-112133195 chr2:112133185-112133196 chr2:112133184-112133197 chr2:112133186-112133195 chr2:112133184-112133197 chr2:112133186-112133195
47	CEBPB	chr2:112132956-112133341	K562	blood:	n/a	chr2:112133186-112133195 chr2:112133185-112133196 chr2:112133184-112133197 chr2:112133186-112133195 chr2:112133184-112133197 chr2:112133186-112133195
48	CEBPB	chr2:112061597-112061658	HepG2	liver:	n/a	chr2:112061630-112061641
49	CEBPB	chr2:112078572-112078922	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr2:112132929-112133356	K562	blood:	n/a	chr2:112133186-112133195 chr2:112133185-112133196 chr2:112133184-112133197 chr2:112133186-112133195 chr2:112133184-112133197 chr2:112133186-112133195

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:112124118-112124168	HNPCEpiC	eye:	n/a
2	chr2:112124118-112124168	BJ	skin:	n/a
3	chr2:112124118-112124168	CMK	blood:	n/a
4	chr2:112124380-112124430	AG10803	skin:	n/a
5	chr2:112124380-112124430	GM06990	blood:	n/a
6	chr2:112124118-112124168	Jurkat	blood:	n/a
7	chr2:112124118-112124168	AG09309	skin:	n/a
8	chr2:112124118-112124168	SAEC	small airway:	n/a
9	chr2:112124380-112124430	RPTEC	kidney:	n/a
10	chr2:112124380-112124430	BE2_C	brain:	n/a
11	chr2:112124380-112124430	Caco-2	colon:	n/a
12	chr2:112124118-112124168	AoSMC	blood vessel:	n/a
13	chr2:112124380-112124430	PANC-1	pancreas:	n/a
14	chr2:112124380-112124430	AG09309	skin:	n/a
15	chr2:112124380-112124430	PrEC	prostate:	n/a
16	chr2:112124380-112124430	HRE	kidney:	n/a
17	chr2:112124380-112124430	AG09319	gingival:	n/a
18	chr2:112124118-112124168	PrEC	prostate:	n/a
19	chr2:112124118-112124168	HL-60	blood:	n/a
20	chr2:112124380-112124430	NHBE	bronchial:	n/a
21	chr2:112124380-112124430	NB4	blood:	n/a
22	chr2:112124118-112124168	AG04450	lung:	fetal
23	chr2:112124118-112124168	K562	blood:	n/a
24	chr2:112124380-112124430	MCF-7	breast:	n/a
25	chr2:112124380-112124430	T-47D	breast:	n/a
26	chr2:112124118-112124168	AG09319	gingival:	n/a
27	chr2:112124118-112124168	H1-hESC	embryonic stem cell:	embryo
28	chr2:112124380-112124430	PFSK-1	brain:	n/a
29	chr2:112124118-112124168	NH-A	brain:	n/a
30	chr2:112124380-112124430	HNPCEpiC	eye:	n/a
31	chr2:112124380-112124430	HIPEpiC	eye:	n/a
32	chr2:112124118-112124168	RPTEC	kidney:	n/a
33	chr2:112124380-112124430	HCF	heart:	n/a
34	chr2:112124380-112124430	HL-60	blood:	n/a
35	chr2:112124380-112124430	A549	lung:	n/a
36	chr2:112124380-112124430	GM19239	blood:	n/a
37	chr2:112124118-112124168	HRPEpiC	eye:	n/a
38	chr2:112124118-112124168	LNCaP	prostate:	n/a
39	chr2:112124380-112124430	SK-N-SH	brain:	n/a
40	chr2:112124380-112124430	HEEpiC	esophagus:	n/a
41	chr2:112124118-112124168	ovcar-3	ovarian:	n/a
42	chr2:112124118-112124168	HepG2	liver:	n/a
43	chr2:112124380-112124430	Hela-S3	cervix:	n/a
44	chr2:112124380-112124430	AG04450	lung:	fetal
45	chr2:112124380-112124430	NHDF-neo	bronchial:	n/a
46	chr2:112124118-112124168	SK-N-SH	brain:	n/a
47	chr2:112124380-112124430	NH-A	brain:	n/a
48	chr2:112124118-112124168	GM12891	blood:	n/a
49	chr2:112124118-112124168	HUVEC	blood vessel:	n/a
50	chr2:112124118-112124168	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr2:111878316..111879893-chr2:112101721..112103928,2	MCF-7	breast:
2	chr2:112158086..112161064-chr8:43095226..43096729,2	MCF-7	breast:
3	chr2:111879395..111881005-chr2:112073345..112075122,2	MCF-7	breast:

(count:33 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC108463.1-3	chr2:112108185-112108338	ENSG00000172965.6
2	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
3	lnc-AC108463.1-3	chr2:112125088-112125152	NONHSAT073639
4	lnc-BCL2L11-5	chr2:112081840-112081972	l_1923_chr2:112081839-112086268_testes
5	lnc-BCL2L11-7	chr2:112141383-112141840	NONHSAT147111
6	lnc-AC108463.1-3	chr2:112071889-112072139	ENSG00000172965.6
7	lnc-AC108463.1-6	chr2:112053206-112053623	NONHSAT073635
8	lnc-AC108463.1-3	chr2:112101789-112101814	NONHSAT073639
9	lnc-BCL2L11-5	chr2:112081889-112082063	NONHSAT073637
10	lnc-BCL2L11-6	chr2:112124594-112124991	NONHSAT073618
11	lnc-AC108463.1-3	chr2:112124591-112125152	NONHSAT073640
12	lnc-BCL2L11-5	chr2:112085950-112086268	l_1923_chr2:112081839-112086268_testes
13	lnc-AC108463.1-3	chr2:112101638-112101814	NONHSAT073622
14	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.10
15	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
16	lnc-AC108463.1-3	chr2:112101668-112101814	ENSG00000172965.6
17	lnc-AC108463.1-3	chr2:112125064-112125102	ENSG00000172965.10
18	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
19	lnc-BCL2L11-5	chr2:112081976-112082063	l_1923_chr2:112081839-112086268_testes
20	lnc-AC108463.1-3	chr2:112101638-112101701	NONHSAT073620
21	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
22	lnc-BCL2L11-6	chr2:112080919-112081327	NONHSAT073618
23	lnc-BCL2L11-7	chr2:112141329-112142569	NONHSAT073641
24	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
25	lnc-BCL2L11-6	chr2:112060981-112061323	NONHSAT073618
26	lnc-AC108463.1-3	chr2:112125064-112125152	NONHSAT073622
27	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
28	lnc-BCL2L11-5	chr2:112085950-112086566	NONHSAT073637
29	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
30	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
31	lnc-AC108463.1-3	chr2:112101638-112101675	ENSG00000172965.10
32	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
33	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4435	chr2:112078638-112078659	MIMAT0018951_1

No data

Variant related genes	Relation type
RPS14P4	TF binding region
MIR4435-1HG	TF binding region
ENSG00000223973	TF binding region
MIR4435-1	TF binding region
RPS14P4	CpG island
MIR4435-1HG	CpG island
ENSG00000223973	CpG island
MIR4435-1	CpG island
ENSG00000153094	chromatin interactions

Extended variants
information (count: 2686 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:2686 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56077498	chr2:112052955-112052956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs547471234	chr2:112052994-112052995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567295231	chr2:112053051-112053052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530304853	chr2:112053065-112053066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149523422	chr2:112053121-112053122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs149315692	chr2:112053173-112053174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569990284	chr2:112053182-112053183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538966335	chr2:112053267-112053268	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs4553828	chr2:112053278-112053279	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs375639600	chr2:112053312-112053313	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs4371359	chr2:112053352-112053353	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs566076728	chr2:112053363-112053364	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs534764488	chr2:112053372-112053373	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs555045678	chr2:112053435-112053436	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs369692078	chr2:112053453-112053454	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs373473527	chr2:112053454-112053455	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs540562471	chr2:112053455-112053456	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs113210524	chr2:112053458-112053459	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs201232819	chr2:112053583-112053584	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs574878011	chr2:112053600-112053601	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs542793213	chr2:112053636-112053637	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs556422160	chr2:112053660-112053661	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs148029388	chr2:112053670-112053671	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs576377274	chr2:112053682-112053683	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs545331439	chr2:112053703-112053704	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs564821670	chr2:112053711-112053712	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs527275606	chr2:112053859-112053860	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs540709902	chr2:112053886-112053887	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs62161608	chr2:112053891-112053892	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs529777241	chr2:112053913-112053914	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs200035284	chr2:112053987-112053988	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs116834718	chr2:112054101-112054102	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs150709727	chr2:112054117-112054118	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs552458183	chr2:112054143-112054144	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs566294046	chr2:112054144-112054145	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs535009860	chr2:112054171-112054172	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs113407391	chr2:112054497-112054498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554702061	chr2:112054630-112054631	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs568521082	chr2:112054658-112054659	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs6747162	chr2:112054665-112054666	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs556359564	chr2:112054676-112054677	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs576307195	chr2:112054708-112054709	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs545269661	chr2:112054711-112054712	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs562220939	chr2:112054715-112054716	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs57979745	chr2:112054719-112054720	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs558804124	chr2:112054725-112054726	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs572283136	chr2:112054730-112054731	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs59371312	chr2:112054739-112054740	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs542268524	chr2:112054755-112054756	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs4849546	chr2:112054761-112054762	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Breast cancer	22314128	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:639 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:112025600-112116600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr2:112046400-112057400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr2:112048800-112069600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr2:112049800-112059800	Weak transcription	HSMMtube	muscle
5	chr2:112051000-112058200	Weak transcription	HepG2	liver
6	chr2:112053200-112053400	Enhancers	Primary B cells from peripheral blood	blood
7	chr2:112053200-112053600	Enhancers	Lung	lung
8	chr2:112053200-112053800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr2:112055000-112070600	Weak transcription	NHLF	lung
10	chr2:112055800-112056200	Weak transcription	HSMM	muscle
11	chr2:112056200-112056800	ZNF genes & repeats	HSMM	muscle
12	chr2:112056800-112059800	Weak transcription	HSMM	muscle
13	chr2:112057400-112057600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr2:112057600-112058000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr2:112058000-112058200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr2:112058000-112058200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr2:112058200-112058600	Enhancers	HepG2	liver
18	chr2:112058200-112069600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr2:112058200-112071000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr2:112058600-112068400	Weak transcription	HepG2	liver
21	chr2:112059800-112060400	Enhancers	HSMMtube	muscle
22	chr2:112059800-112060600	Enhancers	Left Ventricle	heart
23	chr2:112059800-112060800	Enhancers	Fetal Thymus	thymus
24	chr2:112059800-112061000	Enhancers	Dnd41	blood
25	chr2:112059800-112061000	Enhancers	HSMM	muscle
26	chr2:112060000-112060800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr2:112060400-112079200	Weak transcription	HSMMtube	muscle
28	chr2:112060600-112060800	Enhancers	NH-A	brain
29	chr2:112060800-112062600	Weak transcription	NH-A	brain
30	chr2:112062200-112062400	Enhancers	Osteobl	bone
31	chr2:112062200-112062800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr2:112062400-112070200	Weak transcription	Osteobl	bone
33	chr2:112062600-112062800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr2:112062600-112062800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr2:112062600-112062800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr2:112062600-112062800	Enhancers	NH-A	brain
37	chr2:112062800-112063400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr2:112062800-112070600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr2:112062800-112070600	Weak transcription	NH-A	brain
40	chr2:112063000-112067200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr2:112063400-112063600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr2:112063600-112070000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr2:112063600-112086200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr2:112066800-112067000	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr2:112067200-112067400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr2:112067200-112067400	Enhancers	Fetal Muscle Leg	muscle
47	chr2:112067200-112068600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr2:112067400-112069600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr2:112067400-112070400	Weak transcription	Fetal Muscle Leg	muscle
50	chr2:112068000-112068200	Enhancers	Primary neutrophils fromperipheralblood	blood

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