Variant report

Variant	nsv998690
Chromosome Location	chr2:112119611-112196221
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:925)
CpG islands
(count:122)
Chromatin interactive
region (count:1)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:925 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:112134733-112134923	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:112191601-112191749	K562	blood:	n/a	n/a
3	ARID3A	chr2:112142989-112143245	K562	blood:	n/a	n/a
4	ARID3A	chr2:112165582-112165606	K562	blood:	n/a	n/a
5	ATF1	chr2:112191568-112191846	K562	blood:	n/a	n/a
6	ATF1	chr2:112174026-112174226	K562	blood:	n/a	n/a
7	ATF1	chr2:112174751-112174909	K562	blood:	n/a	n/a
8	ATF1	chr2:112123600-112123901	K562	blood:	n/a	n/a
9	ATF1	chr2:112165410-112165614	K562	blood:	n/a	n/a
10	ATF1	chr2:112139588-112139732	K562	blood:	n/a	n/a
11	ATF2	chr2:112183348-112183699	GM12878	blood:	n/a	n/a
12	ATF2	chr2:112183361-112183645	GM12878	blood:	n/a	n/a
13	BACH1	chr2:112143146-112143417	K562	blood:	n/a	n/a
14	BATF	chr2:112158868-112159229	GM12878	blood:	n/a	chr2:112159209-112159219
15	BATF	chr2:112183233-112184090	GM12878	blood:	n/a	n/a
16	BATF	chr2:112188889-112189327	GM12878	blood:	n/a	n/a
17	BATF	chr2:112193934-112194446	GM12878	blood:	n/a	chr2:112194264-112194272
18	BATF	chr2:112182048-112182971	GM12878	blood:	n/a	n/a
19	BATF	chr2:112186949-112187402	GM12878	blood:	n/a	n/a
20	BATF	chr2:112195786-112196106	GM12878	blood:	n/a	n/a
21	BATF	chr2:112169777-112169962	GM12878	blood:	n/a	chr2:112169903-112169914
22	BATF	chr2:112195688-112196162	GM12878	blood:	n/a	n/a
23	BATF	chr2:112193854-112194550	GM12878	blood:	n/a	chr2:112194264-112194272
24	BATF	chr2:112190544-112190853	GM12878	blood:	n/a	n/a
25	BATF	chr2:112195321-112195643	GM12878	blood:	n/a	chr2:112195574-112195583
26	BATF	chr2:112190573-112190841	GM12878	blood:	n/a	n/a
27	BATF	chr2:112183252-112183819	GM12878	blood:	n/a	n/a
28	BATF	chr2:112125762-112126285	GM12878	blood:	n/a	n/a
29	BATF	chr2:112195246-112195683	GM12878	blood:	n/a	chr2:112195574-112195583
30	BATF	chr2:112131695-112131857	GM12878	blood:	n/a	n/a
31	BATF	chr2:112158949-112159184	GM12878	blood:	n/a	n/a
32	BATF	chr2:112182205-112182825	GM12878	blood:	n/a	n/a
33	BATF	chr2:112186898-112187455	GM12878	blood:	n/a	n/a
34	BATF	chr2:112125609-112126213	GM12878	blood:	n/a	chr2:112125629-112125642
35	BATF	chr2:112188947-112189209	GM12878	blood:	n/a	n/a
36	BCL11A	chr2:112194068-112194334	GM12878	blood:	n/a	n/a
37	BCL11A	chr2:112193953-112194442	GM12878	blood:	n/a	n/a
38	BCL11A	chr2:112183223-112183810	GM12878	blood:	n/a	n/a
39	BCL11A	chr2:112195300-112195479	GM12878	blood:	n/a	n/a
40	BCL11A	chr2:112182226-112182918	GM12878	blood:	n/a	n/a
41	BCL11A	chr2:112182331-112182639	GM12878	blood:	n/a	n/a
42	BCL11A	chr2:112125918-112126134	GM12878	blood:	n/a	n/a
43	BCL11A	chr2:112195289-112195669	GM12878	blood:	n/a	n/a
44	BCL11A	chr2:112195836-112195990	GM12878	blood:	n/a	n/a
45	BCL11A	chr2:112188940-112189225	GM12878	blood:	n/a	n/a
46	BCL11A	chr2:112188884-112189288	GM12878	blood:	n/a	n/a
47	BCL11A	chr2:112125764-112126223	GM12878	blood:	n/a	n/a
48	BCL11A	chr2:112186983-112187434	GM12878	blood:	n/a	chr2:112187266-112187275
49	BCL11A	chr2:112195753-112196105	GM12878	blood:	n/a	n/a
50	BCL3	chr2:112183366-112183629	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	chr2:112124380-112124430	H1-hESC	embryonic stem cell:	embryo
2	chr2:112124118-112124168	ECC-1	luminal epithelium:	n/a
3	chr2:112124118-112124168	HNPCEpiC	eye:	n/a
4	chr2:112124118-112124168	PFSK-1	brain:	n/a
5	chr2:112124380-112124430	Hela-S3	cervix:	n/a
6	chr2:112124118-112124168	AG10803	skin:	n/a
7	chr2:112124380-112124430	HCT-116	colon:	n/a
8	chr2:112124380-112124430	GM12891	blood:	n/a
9	chr2:112124380-112124430	SAEC	small airway:	n/a
10	chr2:112124380-112124430	HRPEpiC	eye:	n/a
11	chr2:112124118-112124168	NH-A	brain:	n/a
12	chr2:112124118-112124168	HRPEpiC	eye:	n/a
13	chr2:112124380-112124430	SK-N-MC	brain:	n/a
14	chr2:112124380-112124430	NHDF-neo	bronchial:	n/a
15	chr2:112124380-112124430	T-47D	breast:	n/a
16	chr2:112124118-112124168	BJ	skin:	n/a
17	chr2:112124118-112124168	Caco-2	colon:	n/a
18	chr2:112124380-112124430	HCF	heart:	n/a
19	chr2:112124118-112124168	HPAEpiC	pulmonary alveolar:	n/a
20	chr2:112124380-112124430	PANC-1	pancreas:	n/a
21	chr2:112124118-112124168	NHDF-neo	bronchial:	n/a
22	chr2:112124380-112124430	GM06990	blood:	n/a
23	chr2:112124118-112124168	SKMC	muscle:	n/a
24	chr2:112124380-112124430	NH-A	brain:	n/a
25	chr2:112124118-112124168	HCF	heart:	n/a
26	chr2:112124380-112124430	RPTEC	kidney:	n/a
27	chr2:112124118-112124168	HUVEC	blood vessel:	n/a
28	chr2:112124380-112124430	CMK	blood:	n/a
29	chr2:112124118-112124168	HEEpiC	esophagus:	n/a
30	chr2:112124380-112124430	A549	lung:	n/a
31	chr2:112124380-112124430	NB4	blood:	n/a
32	chr2:112124380-112124430	GM19239	blood:	n/a
33	chr2:112124380-112124430	HAEpiC	amniotic membrane:	n/a
34	chr2:112124118-112124168	SAEC	small airway:	n/a
35	chr2:112124380-112124430	AG09319	gingival:	n/a
36	chr2:112124118-112124168	Hela-S3	cervix:	n/a
37	chr2:112124380-112124430	SKMC	muscle:	n/a
38	chr2:112124118-112124168	PANC-1	pancreas:	n/a
39	chr2:112124118-112124168	Jurkat	blood:	n/a
40	chr2:112124118-112124168	PrEC	prostate:	n/a
41	chr2:112124380-112124430	Caco-2	colon:	n/a
42	chr2:112124118-112124168	HL-60	blood:	n/a
43	chr2:112124380-112124430	HL-60	blood:	n/a
44	chr2:112124380-112124430	HIPEpiC	eye:	n/a
45	chr2:112124118-112124168	AG09309	skin:	n/a
46	chr2:112124118-112124168	SK-N-MC	brain:	n/a
47	chr2:112124380-112124430	NHBE	bronchial:	n/a
48	chr2:112124118-112124168	CMK	blood:	n/a
49	chr2:112124380-112124430	HCM	heart:	n/a
50	chr2:112124118-112124168	T-47D	breast:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:112158086..112161064-chr8:43095226..43096729,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC108463.1-3	chr2:112125064-112125152	NONHSAT073622
2	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
3	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
4	lnc-BCL2L11-6	chr2:112124594-112124991	NONHSAT073618
5	lnc-BCL2L11-7	chr2:112141329-112142569	NONHSAT073641
6	lnc-AC108463.1-3	chr2:112186891-112187197	ENSG00000172965.6
7	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
8	lnc-AC108463.1-3	chr2:112124591-112125152	NONHSAT073640
9	lnc-BCL2L11-7	chr2:112141383-112141840	NONHSAT147111
10	lnc-AC108463.1-3	chr2:112125064-112125102	ENSG00000172965.10
11	lnc-AC108463.1-3	chr2:112187020-112187197	ENSG00000172965.6
12	lnc-AC108463.1-3	chr2:112186886-112187197	NONHSAT073642
13	lnc-BCL2L11-8	chr2:112186899-112187197	NONHSAT073647
14	lnc-AC108463.1-3	chr2:112125088-112125152	NONHSAT073639
15	lnc-AC108463.1-3	chr2:112186891-112187197	ENSG00000172965.6
16	lnc-AC108463.1-3	chr2:112187048-112187197	NONHSAT073639
17	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
18	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6

No data

Variant related genes	Relation type
ENSG00000223973	TF binding region
MIR4435-1HG	TF binding region
ENSG00000223973	CpG island
MIR4435-1HG	CpG island

Extended variants
information (count: 1965 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1965 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570953376	chr2:112119623-112119624	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs377763663	chr2:112119630-112119631	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs533640291	chr2:112119715-112119716	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs553476933	chr2:112119738-112119739	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs567502370	chr2:112119743-112119744	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs182785954	chr2:112119804-112119805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs199951707	chr2:112119817-112119818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576667358	chr2:112119839-112119840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545344865	chr2:112119898-112119899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200885293	chr2:112119909-112119910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572518618	chr2:112120032-112120033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541524293	chr2:112120070-112120071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs372680137	chr2:112120265-112120266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs377036592	chr2:112120273-112120274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561384881	chr2:112120346-112120347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs186525900	chr2:112120355-112120356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190262259	chr2:112120356-112120357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs4283430	chr2:112120376-112120377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112919764	chr2:112120485-112120486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182825837	chr2:112120505-112120506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540056615	chr2:112120545-112120546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs145030071	chr2:112120665-112120666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551702622	chr2:112120670-112120671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374868196	chr2:112120671-112120672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377235069	chr2:112120677-112120678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369551097	chr2:112120682-112120683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373738397	chr2:112120683-112120684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376708061	chr2:112120685-112120686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368975974	chr2:112120687-112120688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113117590	chr2:112120696-112120697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370881709	chr2:112120718-112120719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374509363	chr2:112120774-112120775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200013242	chr2:112120779-112120780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547052597	chr2:112120780-112120781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187470989	chr2:112120809-112120810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs75980570	chr2:112120824-112120825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548551166	chr2:112120833-112120834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570270728	chr2:112120880-112120881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs148762065	chr2:112120890-112120891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559328709	chr2:112121027-112121028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572438202	chr2:112121139-112121140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs56193472	chr2:112121171-112121172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555054581	chr2:112121199-112121200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574849195	chr2:112121208-112121209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs543939004	chr2:112121415-112121416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562541413	chr2:112121459-112121460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576215456	chr2:112121654-112121655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544956669	chr2:112121682-112121683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552840051	chr2:112121694-112121695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564849542	chr2:112121802-112121803	Weak transcription Enhancers	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:684 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:112095400-112123600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr2:112104400-112134600	Weak transcription	HSMMtube	muscle
3	chr2:112113800-112191600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr2:112114400-112125800	Weak transcription	A549	lung
5	chr2:112115000-112123600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr2:112115000-112125200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr2:112115000-112125400	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr2:112115000-112125400	Weak transcription	NHEK	skin
9	chr2:112115000-112128000	Weak transcription	HMEC	breast
10	chr2:112115000-112153200	Weak transcription	HSMM	muscle
11	chr2:112115200-112158600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr2:112115400-112126800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr2:112117000-112123800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr2:112117200-112124000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr2:112117200-112124000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr2:112118200-112119800	ZNF genes & repeats	Dnd41	blood
17	chr2:112119400-112119800	ZNF genes & repeats	K562	blood
18	chr2:112119400-112123600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr2:112119600-112125000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr2:112119800-112123200	Weak transcription	K562	blood
21	chr2:112119800-112136400	Weak transcription	Dnd41	blood
22	chr2:112121800-112122200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr2:112121800-112122400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr2:112122200-112123600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr2:112122400-112123400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr2:112123200-112123400	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr2:112123200-112123600	Enhancers	K562	blood
28	chr2:112123400-112123800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr2:112123600-112123800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
30	chr2:112123600-112123800	Flanking Active TSS	Brain Cingulate Gyrus	brain
31	chr2:112123600-112123800	Enhancers	Left Ventricle	heart
32	chr2:112123600-112123800	Flanking Active TSS	K562	blood
33	chr2:112123600-112123800	Bivalent/Poised TSS	Monocytes-CD14+_RO01746	blood
34	chr2:112123600-112124000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr2:112123600-112124000	Enhancers	Primary B cells from peripheral blood	blood
36	chr2:112123600-112124000	Active TSS	Primary T cells from cord blood	blood
37	chr2:112123600-112124000	Enhancers	Primary hematopoietic stem cells	blood
38	chr2:112123600-112124000	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr2:112123600-112124000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr2:112123600-112124000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
41	chr2:112123600-112124000	Active TSS	Right Atrium	heart
42	chr2:112123600-112124200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr2:112123600-112124200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr2:112123600-112124200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr2:112123600-112124200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr2:112123600-112124200	Active TSS	Adipose Nuclei	Adipose
47	chr2:112123600-112124200	Active TSS	Stomach Smooth Muscle	stomach
48	chr2:112123600-112124400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr2:112123600-112124400	Active TSS	Fetal Brain Female	brain
50	chr2:112123600-112124600	Enhancers	Primary monocytes fromperipheralblood	blood

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