Variant report

Variant	nsv1001412
Chromosome Location	chr2:112085437-112196221
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1076)
CpG islands
(count:123)
Chromatin interactive
region (count:2)
LncRNA
region (count:32)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1076 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:112142989-112143245	K562	blood:	n/a	n/a
2	ARID3A	chr2:112191601-112191749	K562	blood:	n/a	n/a
3	ARID3A	chr2:112165582-112165606	K562	blood:	n/a	n/a
4	ARID3A	chr2:112134733-112134923	HepG2	liver:	n/a	n/a
5	ATF1	chr2:112104247-112104437	K562	blood:	n/a	n/a
6	ATF1	chr2:112174751-112174909	K562	blood:	n/a	n/a
7	ATF1	chr2:112165410-112165614	K562	blood:	n/a	n/a
8	ATF1	chr2:112191568-112191846	K562	blood:	n/a	n/a
9	ATF1	chr2:112174026-112174226	K562	blood:	n/a	n/a
10	ATF1	chr2:112123600-112123901	K562	blood:	n/a	n/a
11	ATF1	chr2:112139588-112139732	K562	blood:	n/a	n/a
12	ATF2	chr2:112183361-112183645	GM12878	blood:	n/a	n/a
13	ATF2	chr2:112183348-112183699	GM12878	blood:	n/a	n/a
14	BACH1	chr2:112143146-112143417	K562	blood:	n/a	n/a
15	BATF	chr2:112183233-112184090	GM12878	blood:	n/a	n/a
16	BATF	chr2:112125762-112126285	GM12878	blood:	n/a	n/a
17	BATF	chr2:112195786-112196106	GM12878	blood:	n/a	n/a
18	BATF	chr2:112183252-112183819	GM12878	blood:	n/a	n/a
19	BATF	chr2:112131695-112131857	GM12878	blood:	n/a	n/a
20	BATF	chr2:112188947-112189209	GM12878	blood:	n/a	n/a
21	BATF	chr2:112190573-112190841	GM12878	blood:	n/a	n/a
22	BATF	chr2:112195246-112195683	GM12878	blood:	n/a	chr2:112195574-112195583
23	BATF	chr2:112190544-112190853	GM12878	blood:	n/a	n/a
24	BATF	chr2:112182048-112182971	GM12878	blood:	n/a	n/a
25	BATF	chr2:112125609-112126213	GM12878	blood:	n/a	chr2:112125629-112125642
26	BATF	chr2:112186949-112187402	GM12878	blood:	n/a	n/a
27	BATF	chr2:112195688-112196162	GM12878	blood:	n/a	n/a
28	BATF	chr2:112195321-112195643	GM12878	blood:	n/a	chr2:112195574-112195583
29	BATF	chr2:112193854-112194550	GM12878	blood:	n/a	chr2:112194264-112194272
30	BATF	chr2:112186898-112187455	GM12878	blood:	n/a	n/a
31	BATF	chr2:112169777-112169962	GM12878	blood:	n/a	chr2:112169903-112169914
32	BATF	chr2:112158868-112159229	GM12878	blood:	n/a	chr2:112159209-112159219
33	BATF	chr2:112158949-112159184	GM12878	blood:	n/a	n/a
34	BATF	chr2:112193934-112194446	GM12878	blood:	n/a	chr2:112194264-112194272
35	BATF	chr2:112188889-112189327	GM12878	blood:	n/a	n/a
36	BATF	chr2:112182205-112182825	GM12878	blood:	n/a	n/a
37	BCL11A	chr2:112125918-112126134	GM12878	blood:	n/a	n/a
38	BCL11A	chr2:112195836-112195990	GM12878	blood:	n/a	n/a
39	BCL11A	chr2:112186983-112187434	GM12878	blood:	n/a	chr2:112187266-112187275
40	BCL11A	chr2:112193953-112194442	GM12878	blood:	n/a	n/a
41	BCL11A	chr2:112195300-112195479	GM12878	blood:	n/a	n/a
42	BCL11A	chr2:112087560-112087812	GM12878	blood:	n/a	n/a
43	BCL11A	chr2:112194068-112194334	GM12878	blood:	n/a	n/a
44	BCL11A	chr2:112183223-112183810	GM12878	blood:	n/a	n/a
45	BCL11A	chr2:112195753-112196105	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	chr2:112182331-112182639	GM12878	blood:	n/a	n/a
49	BCL11A	chr2:112188940-112189225	GM12878	blood:	n/a	n/a
50	BCL11A	chr2:112195289-112195669	GM12878	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:112124380-112124430	BE2_C	brain:	n/a
2	chr2:112124380-112124430	BE2_C	brain:	n/a
3	chr2:112124118-112124168	AG09309	skin:	n/a
4	chr2:112124118-112124168	NB4	blood:	n/a
5	chr2:112124118-112124168	AG04449	skin:	fetal
6	chr2:112124380-112124430	HRE	kidney:	n/a
7	chr2:112124380-112124430	U87	brain:	n/a
8	chr2:112124118-112124168	SKMC	muscle:	n/a
9	chr2:112124118-112124168	SK-N-SH_RA	brain:	n/a
10	chr2:112124118-112124168	MCF10A-Er-Src	breast:	n/a
11	chr2:112124380-112124430	HCF	heart:	n/a
12	chr2:112124380-112124430	HRPEpiC	eye:	n/a
13	chr2:112124118-112124168	HRE	kidney:	n/a
14	chr2:112124380-112124430	HPAEpiC	pulmonary alveolar:	n/a
15	chr2:112124380-112124430	GM19239	blood:	n/a
16	chr2:112124380-112124430	CMK	blood:	n/a
17	chr2:112124118-112124168	Hepatocyte	liver:	n/a
18	chr2:112124380-112124430	HEEpiC	esophagus:	n/a
19	chr2:112124118-112124168	SAEC	small airway:	n/a
20	chr2:112124380-112124430	HCM	heart:	n/a
21	chr2:112124380-112124430	AG10803	skin:	n/a
22	chr2:112124118-112124168	NT2-D1	testis:	n/a
23	chr2:112124118-112124168	SK-N-SH	brain:	n/a
24	chr2:112124118-112124168	HPAEpiC	pulmonary alveolar:	n/a
25	chr2:112124380-112124430	NB4	blood:	n/a
26	chr2:112124118-112124168	T-47D	breast:	n/a
27	chr2:112124118-112124168	PANC-1	pancreas:	n/a
28	chr2:112124118-112124168	Jurkat	blood:	n/a
29	chr2:112124380-112124430	AoSMC	blood vessel:	n/a
30	chr2:112124380-112124430	NHBE	bronchial:	n/a
31	chr2:112124118-112124168	ProgFib	skin:	n/a
32	chr2:112124118-112124168	CMK	blood:	n/a
33	chr2:112124380-112124430	GM12892	blood:	n/a
34	chr2:112124118-112124168	H1-hESC	embryonic stem cell:	embryo
35	chr2:112124118-112124168	HAEpiC	amniotic membrane:	n/a
36	chr2:112124380-112124430	SAEC	small airway:	n/a
37	chr2:112124118-112124168	PFSK-1	brain:	n/a
38	chr2:112124118-112124168	A549	lung:	n/a
39	chr2:112124380-112124430	H1-hESC	embryonic stem cell:	embryo
40	chr2:112124380-112124430	LNCaP	prostate:	n/a
41	chr2:112124380-112124430	AG04449	skin:	fetal
42	chr2:112124118-112124168	RPTEC	kidney:	n/a
43	chr2:112124118-112124168	IMR90	lung:	fetal
44	chr2:112124118-112124168	HCT-116	colon:	n/a
45	chr2:112124118-112124168	Hela-S3	cervix:	n/a
46	chr2:112124118-112124168	HCM	heart:	n/a
47	chr2:112124380-112124430	HCT-116	colon:	n/a
48	chr2:112124380-112124430	A549	lung:	n/a
49	chr2:112124118-112124168	AoSMC	blood vessel:	n/a
50	chr2:112124118-112124168	HRCEpiC	kidney:	n/a

(count:2 , 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:
2	chr2:111878316..111879893-chr2:112101721..112103928,2	MCF-7	breast:

(count:32 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
2	lnc-BCL2L11-7	chr2:112141383-112141840	NONHSAT147111
3	lnc-BCL2L11-7	chr2:112141329-112142569	NONHSAT073641
4	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
5	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
6	lnc-AC108463.1-3	chr2:112186886-112187197	NONHSAT073642
7	lnc-AC108463.1-3	chr2:112125088-112125152	NONHSAT073639
8	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
9	lnc-AC108463.1-3	chr2:112101668-112101814	ENSG00000172965.6
10	lnc-BCL2L11-5	chr2:112085950-112086268	l_1923_chr2:112081839-112086268_testes
11	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
12	lnc-AC108463.1-3	chr2:112101638-112101814	NONHSAT073622
13	lnc-BCL2L11-5	chr2:112085950-112086566	NONHSAT073637
14	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
15	lnc-BCL2L11-6	chr2:112124594-112124991	NONHSAT073618
16	lnc-AC108463.1-3	chr2:112187048-112187197	NONHSAT073639
17	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
18	lnc-AC108463.1-3	chr2:112108185-112108338	ENSG00000172965.6
19	lnc-AC108463.1-3	chr2:112101638-112101701	NONHSAT073620
20	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
21	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
22	lnc-BCL2L11-8	chr2:112186899-112187197	NONHSAT073647
23	lnc-AC108463.1-3	chr2:112186891-112187197	ENSG00000172965.6
24	lnc-AC108463.1-3	chr2:112124591-112125152	NONHSAT073640
25	lnc-AC108463.1-3	chr2:112187020-112187197	ENSG00000172965.6
26	lnc-AC108463.1-3	chr2:112186891-112187197	ENSG00000172965.6
27	lnc-AC108463.1-3	chr2:112101789-112101814	NONHSAT073639
28	lnc-AC108463.1-3	chr2:112125064-112125152	NONHSAT073622
29	lnc-AC108463.1-3	chr2:112101638-112101675	ENSG00000172965.10
30	lnc-AC108463.1-3	chr2:112125064-112125102	ENSG00000172965.10
31	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.10
32	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6

No data

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

Extended variants
information (count: 2639 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:2639 , 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	rs62162899	chr2:112085487-112085488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs77037715	chr2:112085948-112085949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200752827	chr2:112085974-112085975	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs201887422	chr2:112086055-112086056	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs199559525	chr2:112086233-112086234	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs62162900	chr2:112086285-112086286	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs62162901	chr2:112086365-112086366	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs62162903	chr2:112087470-112087471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs62162904	chr2:112087489-112087490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs62162905	chr2:112087504-112087505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs62162906	chr2:112087906-112087907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs62162907	chr2:112088001-112088002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs62162908	chr2:112088147-112088148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs62162909	chr2:112088223-112088224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs62162910	chr2:112088281-112088282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200616512	chr2:112088433-112088434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200631545	chr2:112088635-112088636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142630474	chr2:112088637-112088638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148001101	chr2:112088638-112088639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs530570559	chr2:112088690-112088691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113581373	chr2:112088697-112088698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550689211	chr2:112088745-112088746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564206856	chr2:112088890-112088891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533534420	chr2:112088891-112088892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201502322	chr2:112088964-112088965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547228393	chr2:112089124-112089125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139700255	chr2:112089139-112089140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201962247	chr2:112089165-112089166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs62162912	chr2:112089227-112089228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201831036	chr2:112089255-112089256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs56357530	chr2:112089267-112089268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs535774493	chr2:112089271-112089272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549697252	chr2:112089275-112089276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs62162913	chr2:112089604-112089605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569148480	chr2:112089612-112089613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537883199	chr2:112089700-112089701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs62162914	chr2:112089709-112089710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373157203	chr2:112089748-112089749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113581291	chr2:112089765-112089766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs557808618	chr2:112089814-112089815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs202133676	chr2:112089867-112089868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577737112	chr2:112089875-112089876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539214229	chr2:112089910-112089911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200524608	chr2:112089925-112089926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552902867	chr2:112089929-112089930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200381103	chr2:112089940-112089941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs58213397	chr2:112090022-112090023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201451637	chr2:112090029-112090030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541758340	chr2:112090066-112090067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562058536	chr2:112090083-112090084	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:834 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:112025600-112116600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr2:112063600-112086200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr2:112071400-112102400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr2:112073400-112087000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr2:112078400-112103800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr2:112079400-112104000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr2:112080400-112090800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr2:112089400-112101800	Weak transcription	Dnd41	blood
9	chr2:112095400-112123600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr2:112096000-112103800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr2:112096000-112104000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr2:112098600-112116600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr2:112099000-112099200	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr2:112099000-112099200	Enhancers	NH-A	brain
15	chr2:112099200-112102200	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr2:112099200-112104200	Weak transcription	HSMMtube	muscle
17	chr2:112099600-112102400	Weak transcription	NH-A	brain
18	chr2:112099800-112103800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr2:112100000-112103800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr2:112102200-112102600	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr2:112102200-112102800	Enhancers	Muscle Satellite Cultured Cells	--
22	chr2:112102200-112104400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr2:112102400-112102600	Enhancers	NH-A	brain
24	chr2:112102400-112102800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr2:112102400-112102800	Enhancers	K562	blood
26	chr2:112102400-112102800	Enhancers	NHDF-Ad	bronchial
27	chr2:112102400-112103400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr2:112102400-112105200	Enhancers	HUVEC	blood vessel
29	chr2:112102600-112103800	Weak transcription	NH-A	brain
30	chr2:112102600-112104800	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr2:112102800-112103800	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr2:112102800-112104000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr2:112102800-112104800	Weak transcription	K562	blood
34	chr2:112102800-112104800	Weak transcription	NHDF-Ad	bronchial
35	chr2:112103000-112104600	Enhancers	Osteobl	bone
36	chr2:112103800-112104000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr2:112103800-112104000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr2:112103800-112104200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr2:112103800-112104200	Enhancers	Fetal Muscle Trunk	muscle
40	chr2:112103800-112104200	Enhancers	Skeletal Muscle Male	skeletal muscle
41	chr2:112103800-112104400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr2:112103800-112104400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr2:112103800-112104400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr2:112103800-112104600	Enhancers	NH-A	brain
45	chr2:112103800-112105200	Enhancers	Muscle Satellite Cultured Cells	--
46	chr2:112104000-112104200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr2:112104000-112104400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr2:112104000-112104400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr2:112104000-112104400	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr2:112104000-112104400	Enhancers	Fetal Muscle Leg	muscle

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