Variant report

Variant	nsv1011640
Chromosome Location	chr2:112050871-112196221
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1366)
CpG islands
(count:122)
Chromatin interactive
region (count:3)
LncRNA
region (count:39)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1366 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:112165582-112165606	K562	blood:	n/a	n/a
2	ARID3A	chr2:112134733-112134923	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:112191601-112191749	K562	blood:	n/a	n/a
4	ARID3A	chr2:112078700-112078866	K562	blood:	n/a	n/a
5	ARID3A	chr2:112142989-112143245	K562	blood:	n/a	n/a
6	ARID3A	chr2:112077982-112078035	K562	blood:	n/a	n/a
7	ATF1	chr2:112139588-112139732	K562	blood:	n/a	n/a
8	ATF1	chr2:112123600-112123901	K562	blood:	n/a	n/a
9	ATF1	chr2:112191568-112191846	K562	blood:	n/a	n/a
10	ATF1	chr2:112174751-112174909	K562	blood:	n/a	n/a
11	ATF1	chr2:112104247-112104437	K562	blood:	n/a	n/a
12	ATF1	chr2:112174026-112174226	K562	blood:	n/a	n/a
13	ATF1	chr2:112165410-112165614	K562	blood:	n/a	n/a
14	ATF2	chr2:112183361-112183645	GM12878	blood:	n/a	n/a
15	ATF2	chr2:112183348-112183699	GM12878	blood:	n/a	n/a
16	BACH1	chr2:112078641-112078944	K562	blood:	n/a	chr2:112078792-112078806
17	BACH1	chr2:112143146-112143417	K562	blood:	n/a	n/a
18	BACH1	chr2:112078561-112079019	H1-hESC	embryonic stem cell:	n/a	chr2:112078792-112078806
19	BATF	chr2:112077128-112077551	GM12878	blood:	n/a	n/a
20	BATF	chr2:112158949-112159184	GM12878	blood:	n/a	n/a
21	BATF	chr2:112195688-112196162	GM12878	blood:	n/a	n/a
22	BATF	chr2:112186949-112187402	GM12878	blood:	n/a	n/a
23	BATF	chr2:112125762-112126285	GM12878	blood:	n/a	n/a
24	BATF	chr2:112188947-112189209	GM12878	blood:	n/a	n/a
25	BATF	chr2:112195246-112195683	GM12878	blood:	n/a	chr2:112195574-112195583
26	BATF	chr2:112072847-112073098	GM12878	blood:	n/a	chr2:112073011-112073022 chr2:112072925-112072935
27	BATF	chr2:112195786-112196106	GM12878	blood:	n/a	n/a
28	BATF	chr2:112190573-112190841	GM12878	blood:	n/a	n/a
29	BATF	chr2:112158868-112159229	GM12878	blood:	n/a	chr2:112159209-112159219
30	BATF	chr2:112195321-112195643	GM12878	blood:	n/a	chr2:112195574-112195583
31	BATF	chr2:112074635-112074933	GM12878	blood:	n/a	chr2:112074773-112074784
32	BATF	chr2:112190544-112190853	GM12878	blood:	n/a	n/a
33	BATF	chr2:112188889-112189327	GM12878	blood:	n/a	n/a
34	BATF	chr2:112183233-112184090	GM12878	blood:	n/a	n/a
35	BATF	chr2:112182048-112182971	GM12878	blood:	n/a	n/a
36	BATF	chr2:112125609-112126213	GM12878	blood:	n/a	chr2:112125629-112125642
37	BATF	chr2:112183252-112183819	GM12878	blood:	n/a	n/a
38	BATF	chr2:112193854-112194550	GM12878	blood:	n/a	chr2:112194264-112194272
39	BATF	chr2:112169777-112169962	GM12878	blood:	n/a	chr2:112169903-112169914
40	BATF	chr2:112186898-112187455	GM12878	blood:	n/a	n/a
41	BATF	chr2:112072875-112073150	GM12878	blood:	n/a	chr2:112073011-112073022 chr2:112072925-112072935
42	BATF	chr2:112077193-112077517	GM12878	blood:	n/a	n/a
43	BATF	chr2:112193934-112194446	GM12878	blood:	n/a	chr2:112194264-112194272
44	BATF	chr2:112182205-112182825	GM12878	blood:	n/a	n/a
45	BATF	chr2:112074557-112074916	GM12878	blood:	n/a	chr2:112074773-112074784
46	BATF	chr2:112073963-112074275	GM12878	blood:	n/a	n/a
47	BATF	chr2:112131695-112131857	GM12878	blood:	n/a	n/a
48	BCL11A	chr2:112195289-112195669	GM12878	blood:	n/a	n/a
49	BCL11A	chr2:112072754-112073092	GM12878	blood:	n/a	chr2:112072837-112072846
50	BCL11A	chr2:112193953-112194442	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:112124118-112124168	PrEC	prostate:	n/a
2	chr2:112124118-112124168	SK-N-MC	brain:	n/a
3	chr2:112124118-112124168	HRCEpiC	kidney:	n/a
4	chr2:112124380-112124430	Hela-S3	cervix:	n/a
5	chr2:112124118-112124168	BJ	skin:	n/a
6	chr2:112124380-112124430	HIPEpiC	eye:	n/a
7	chr2:112124380-112124430	HCT-116	colon:	n/a
8	chr2:112124380-112124430	AG04449	skin:	fetal
9	chr2:112124380-112124430	AG10803	skin:	n/a
10	chr2:112124380-112124430	GM12892	blood:	n/a
11	chr2:112124380-112124430	NH-A	brain:	n/a
12	chr2:112124118-112124168	SK-N-SH	brain:	n/a
13	chr2:112124380-112124430	HCM	heart:	n/a
14	chr2:112124380-112124430	SK-N-SH	brain:	n/a
15	chr2:112124118-112124168	HCM	heart:	n/a
16	chr2:112124118-112124168	BE2_C	brain:	n/a
17	chr2:112124380-112124430	SK-N-MC	brain:	n/a
18	chr2:112124380-112124430	IMR90	lung:	fetal
19	chr2:112124380-112124430	RPTEC	kidney:	n/a
20	chr2:112124118-112124168	HepG2	liver:	n/a
21	chr2:112124380-112124430	AoSMC	blood vessel:	n/a
22	chr2:112124380-112124430	HEEpiC	esophagus:	n/a
23	chr2:112124380-112124430	T-47D	breast:	n/a
24	chr2:112124118-112124168	ovcar-3	ovarian:	n/a
25	chr2:112124118-112124168	HEEpiC	esophagus:	n/a
26	chr2:112124118-112124168	HMEC	breast:	n/a
27	chr2:112124380-112124430	HNPCEpiC	eye:	n/a
28	chr2:112124380-112124430	ovcar-3	ovarian:	n/a
29	chr2:112124380-112124430	PANC-1	pancreas:	n/a
30	chr2:112124118-112124168	LNCaP	prostate:	n/a
31	chr2:112124118-112124168	GM06990	blood:	n/a
32	chr2:112124380-112124430	HEK293	kidney:	embryo
33	chr2:112124380-112124430	ProgFib	skin:	n/a
34	chr2:112124380-112124430	HAEpiC	amniotic membrane:	n/a
35	chr2:112124380-112124430	SAEC	small airway:	n/a
36	chr2:112124380-112124430	NHBE	bronchial:	n/a
37	chr2:112124380-112124430	HRE	kidney:	n/a
38	chr2:112124118-112124168	T-47D	breast:	n/a
39	chr2:112124380-112124430	NHDF-neo	bronchial:	n/a
40	chr2:112124118-112124168	SKMC	muscle:	n/a
41	chr2:112124380-112124430	A549	lung:	n/a
42	chr2:112124118-112124168	NH-A	brain:	n/a
43	chr2:112124118-112124168	HUVEC	blood vessel:	n/a
44	chr2:112124380-112124430	NT2-D1	testis:	n/a
45	chr2:112124118-112124168	ECC-1	luminal epithelium:	n/a
46	chr2:112124118-112124168	MCF-7	breast:	n/a
47	chr2:112124380-112124430	Hepatocyte	liver:	n/a
48	chr2:112124118-112124168	IMR90	lung:	fetal
49	chr2:112124118-112124168	HIPEpiC	eye:	n/a
50	chr2:112124380-112124430	PFSK-1	brain:	n/a

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

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

(count:39 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC108463.1-3	chr2:112125088-112125152	NONHSAT073639
2	lnc-BCL2L11-5	chr2:112085950-112086268	l_1923_chr2:112081839-112086268_testes
3	lnc-AC108463.1-3	chr2:112101638-112101701	NONHSAT073620
4	lnc-AC108463.1-3	chr2:112125064-112125152	NONHSAT073622
5	lnc-BCL2L11-5	chr2:112081976-112082063	l_1923_chr2:112081839-112086268_testes
6	lnc-BCL2L11-7	chr2:112141329-112142569	NONHSAT073641
7	lnc-AC108463.1-3	chr2:112125064-112125102	ENSG00000172965.10
8	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
9	lnc-AC108463.1-3	chr2:112108185-112108338	ENSG00000172965.6
10	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.10
11	lnc-AC108463.1-3	chr2:112101638-112101675	ENSG00000172965.10
12	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
13	lnc-AC108463.1-3	chr2:112101668-112101814	ENSG00000172965.6
14	lnc-BCL2L11-5	chr2:112081889-112082063	NONHSAT073637
15	lnc-AC108463.1-3	chr2:112071889-112072139	ENSG00000172965.6
16	lnc-AC108463.1-6	chr2:112053206-112053623	NONHSAT073635
17	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
18	lnc-BCL2L11-7	chr2:112141383-112141840	NONHSAT147111
19	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
20	lnc-AC108463.1-3	chr2:112186891-112187197	ENSG00000172965.6
21	lnc-AC108463.1-3	chr2:112187048-112187197	NONHSAT073639
22	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
23	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
24	lnc-AC108463.1-3	chr2:112186891-112187197	ENSG00000172965.6
25	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
26	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
27	lnc-AC108463.1-3	chr2:112186886-112187197	NONHSAT073642
28	lnc-BCL2L11-8	chr2:112186899-112187197	NONHSAT073647
29	lnc-BCL2L11-6	chr2:112124594-112124991	NONHSAT073618
30	lnc-BCL2L11-6	chr2:112080919-112081327	NONHSAT073618
31	lnc-AC108463.1-3	chr2:112124591-112125152	NONHSAT073640
32	lnc-BCL2L11-6	chr2:112060981-112061323	NONHSAT073618
33	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
34	lnc-AC108463.1-3	chr2:112101638-112101814	NONHSAT073622
35	lnc-AC108463.1-3	chr2:112101789-112101814	NONHSAT073639
36	lnc-BCL2L11-5	chr2:112081840-112081972	l_1923_chr2:112081839-112086268_testes
37	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
38	lnc-BCL2L11-5	chr2:112085950-112086566	NONHSAT073637
39	lnc-AC108463.1-3	chr2:112187020-112187197	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: 3585 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:3585 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62161604	chr2:112050877-112050878	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs562922346	chr2:112050908-112050909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs145105407	chr2:112050915-112050916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs202078691	chr2:112050926-112050927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533544522	chr2:112050929-112050930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531660575	chr2:112050980-112050981	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545109548	chr2:112051076-112051077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs563893133	chr2:112051130-112051131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201656289	chr2:112051249-112051250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532959244	chr2:112051255-112051256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs368319028	chr2:112051361-112051362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546815987	chr2:112051391-112051392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs199505755	chr2:112051448-112051449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529218182	chr2:112051473-112051474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548670561	chr2:112051542-112051543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568882668	chr2:112051562-112051563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537898311	chr2:112051572-112051573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551502058	chr2:112051587-112051588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs72627493	chr2:112051623-112051624	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs201613121	chr2:112051624-112051625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534382233	chr2:112051631-112051632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554378772	chr2:112051646-112051647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs368184921	chr2:112051807-112051808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201971097	chr2:112051862-112051863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs148996438	chr2:112051866-112051867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556244120	chr2:112051878-112051879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576032423	chr2:112051887-112051888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545048903	chr2:112051902-112051903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565030757	chr2:112051928-112051929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572243119	chr2:112051987-112051988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540034820	chr2:112052034-112052035	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560314451	chr2:112052075-112052076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529138943	chr2:112052076-112052077	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549266385	chr2:112052091-112052092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs562418989	chr2:112052095-112052096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531328941	chr2:112052099-112052100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551435051	chr2:112052104-112052105	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200848467	chr2:112052115-112052116	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564665784	chr2:112052154-112052155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571348178	chr2:112052160-112052161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368761685	chr2:112052183-112052184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533915382	chr2:112052193-112052194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547642533	chr2:112052201-112052202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201346008	chr2:112052241-112052242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536499448	chr2:112052299-112052300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556437928	chr2:112052322-112052323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374681718	chr2:112052355-112052356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538633940	chr2:112052357-112052358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs558558902	chr2:112052431-112052432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572181730	chr2:112052446-112052447	Weak transcription	n/a	n/a	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:1024 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

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	chr2:112047800-112052400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:112048600-112051000	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr2:112048800-112069600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr2:112049400-112051000	Enhancers	HepG2	liver
7	chr2:112049800-112051000	Enhancers	Duodenum Mucosa	Duodenum
8	chr2:112049800-112052000	Weak transcription	Liver	Liver
9	chr2:112049800-112059800	Weak transcription	HSMMtube	muscle
10	chr2:112050600-112051000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr2:112050600-112051000	Enhancers	K562	blood
12	chr2:112050800-112051000	Enhancers	Placenta	Placenta
13	chr2:112050800-112051000	Enhancers	Osteobl	bone
14	chr2:112051000-112052000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr2:112051000-112058200	Weak transcription	HepG2	liver
16	chr2:112052000-112052200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr2:112052000-112052200	Enhancers	Liver	Liver
18	chr2:112053200-112053400	Enhancers	Primary B cells from peripheral blood	blood
19	chr2:112053200-112053600	Enhancers	Lung	lung
20	chr2:112053200-112053800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr2:112055000-112070600	Weak transcription	NHLF	lung
22	chr2:112055800-112056200	Weak transcription	HSMM	muscle
23	chr2:112056200-112056800	ZNF genes & repeats	HSMM	muscle
24	chr2:112056800-112059800	Weak transcription	HSMM	muscle
25	chr2:112057400-112057600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr2:112057600-112058000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr2:112058000-112058200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr2:112058000-112058200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr2:112058200-112058600	Enhancers	HepG2	liver
30	chr2:112058200-112069600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr2:112058200-112071000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr2:112058600-112068400	Weak transcription	HepG2	liver
33	chr2:112059800-112060400	Enhancers	HSMMtube	muscle
34	chr2:112059800-112060600	Enhancers	Left Ventricle	heart
35	chr2:112059800-112060800	Enhancers	Fetal Thymus	thymus
36	chr2:112059800-112061000	Enhancers	Dnd41	blood
37	chr2:112059800-112061000	Enhancers	HSMM	muscle
38	chr2:112060000-112060800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr2:112060400-112079200	Weak transcription	HSMMtube	muscle
40	chr2:112060600-112060800	Enhancers	NH-A	brain
41	chr2:112060800-112062600	Weak transcription	NH-A	brain
42	chr2:112062200-112062400	Enhancers	Osteobl	bone
43	chr2:112062200-112062800	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr2:112062400-112070200	Weak transcription	Osteobl	bone
45	chr2:112062600-112062800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr2:112062600-112062800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr2:112062600-112062800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr2:112062600-112062800	Enhancers	NH-A	brain
49	chr2:112062800-112063400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr2:112062800-112070600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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