Variant report

Variant	nsv873417
Chromosome Location	chr1:246457214-246502153
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:514)
CpG islands
(count:122)
Chromatin interactive
region (count:22)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:514 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:246469874-246470465	K562	blood:	n/a	n/a
2	ARID3A	chr1:246468839-246469426	K562	blood:	n/a	n/a
3	ARID3A	chr1:246476713-246476913	K562	blood:	n/a	n/a
4	ARID3A	chr1:246495436-246495765	K562	blood:	n/a	n/a
5	ARID3A	chr1:246472537-246472962	K562	blood:	n/a	n/a
6	ATF1	chr1:246501515-246501774	K562	blood:	n/a	n/a
7	ATF1	chr1:246495450-246495686	K562	blood:	n/a	n/a
8	ATF1	chr1:246469981-246470295	K562	blood:	n/a	n/a
9	ATF2	chr1:246501723-246502313	GM12878	blood:	n/a	n/a
10	ATF2	chr1:246492949-246493723	GM12878	blood:	n/a	n/a
11	ATF2	chr1:246493100-246493631	GM12878	blood:	n/a	n/a
12	BACH1	chr1:246469926-246470676	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr1:246469042-246469374	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr1:246469053-246469366	K562	blood:	n/a	n/a
15	BACH1	chr1:246469627-246470581	K562	blood:	n/a	n/a
16	BATF	chr1:246493105-246493597	GM12878	blood:	n/a	chr1:246493346-246493357
17	BATF	chr1:246501825-246502142	GM12878	blood:	n/a	n/a
18	BATF	chr1:246493051-246493632	GM12878	blood:	n/a	chr1:246493346-246493357
19	BCL11A	chr1:246493088-246493638	GM12878	blood:	n/a	chr1:246493592-246493599 chr1:246493349-246493358
20	BCL11A	chr1:246493003-246493636	GM12878	blood:	n/a	chr1:246493592-246493599 chr1:246493349-246493358
21	BCL3	chr1:246493055-246493585	GM12878	blood:	n/a	chr1:246493349-246493358
22	BCL3	chr1:246500317-246500521	GM12878	blood:	n/a	n/a
23	BCL3	chr1:246474759-246475054	GM12878	blood:	n/a	n/a
24	BCLAF1	chr1:246493000-246493668	GM12878	blood:	n/a	chr1:246493592-246493599 chr1:246493349-246493358
25	BCLAF1	chr1:246493053-246493656	GM12878	blood:	n/a	chr1:246493592-246493599 chr1:246493349-246493358
26	BHLHE40	chr1:246469899-246470287	K562	blood:	n/a	n/a
27	BHLHE40	chr1:246501857-246502115	GM12878	blood:	n/a	n/a
28	BHLHE40	chr1:246493081-246493626	GM12878	blood:	n/a	n/a
29	BHLHE40	chr1:246495569-246495766	K562	blood:	n/a	n/a
30	BHLHE40	chr1:246501485-246501808	K562	blood:	n/a	n/a
31	CBX3	chr1:246469114-246469749	K562	blood:	n/a	chr1:246469383-246469394
32	CBX3	chr1:246469834-246470418	K562	blood:	n/a	n/a
33	CCNT2	chr1:246495455-246495669	K562	blood:	n/a	n/a
34	CCNT2	chr1:246472666-246473033	K562	blood:	n/a	n/a
35	CCNT2	chr1:246470003-246470249	K562	blood:	n/a	n/a
36	CEBPB	chr1:246464897-246465244	IMR90	lung:	n/a	chr1:246465056-246465067
37	CEBPB	chr1:246483583-246483947	IMR90	lung:	n/a	chr1:246483758-246483769 chr1:246483760-246483769
38	CEBPB	chr1:246493011-246493799	GM12878	blood:	n/a	n/a
39	CEBPB	chr1:246488055-246488337	A549	lung:	n/a	n/a
40	CEBPB	chr1:246495527-246495684	K562	blood:	n/a	n/a
41	CEBPB	chr1:246483696-246483900	HepG2	liver:	n/a	chr1:246483758-246483769 chr1:246483760-246483769
42	CEBPB	chr1:246483728-246483819	H1-hESC	embryonic stem cell:	n/a	chr1:246483758-246483769 chr1:246483760-246483769
43	CEBPB	chr1:246490440-246490704	MCF-7	breast:	n/a	n/a
44	CEBPB	chr1:246501582-246501763	K562	blood:	n/a	n/a
45	CEBPB	chr1:246487659-246487768	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr1:246483598-246483908	K562	blood:	n/a	chr1:246483758-246483769 chr1:246483760-246483769
47	CEBPB	chr1:246474391-246474534	K562	blood:	n/a	n/a
48	CEBPB	chr1:246487962-246488318	A549	lung:	n/a	n/a
49	CEBPB	chr1:246488024-246488342	IMR90	lung:	n/a	n/a
50	CEBPB	chr1:246469261-246469605	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246457244-246457294	ProgFib	skin:	n/a
2	chr1:246457244-246457294	HepG2	liver:	n/a
3	chr1:246466280-246466330	HCF	heart:	n/a
4	chr1:246457244-246457294	SK-N-SH_RA	brain:	n/a
5	chr1:246466280-246466330	NHBE	bronchial:	n/a
6	chr1:246466280-246466330	LNCaP	prostate:	n/a
7	chr1:246457244-246457294	T-47D	breast:	n/a
8	chr1:246457244-246457294	Jurkat	blood:	n/a
9	chr1:246457244-246457294	NB4	blood:	n/a
10	chr1:246466280-246466330	HCT-116	colon:	n/a
11	chr1:246466280-246466330	GM12891	blood:	n/a
12	chr1:246466280-246466330	HMEC	breast:	n/a
13	chr1:246457244-246457294	ovcar-3	ovarian:	n/a
14	chr1:246466280-246466330	PrEC	prostate:	n/a
15	chr1:246457244-246457294	HL-60	blood:	n/a
16	chr1:246466280-246466330	H1-hESC	embryonic stem cell:	embryo
17	chr1:246466280-246466330	HepG2	liver:	n/a
18	chr1:246457244-246457294	PANC-1	pancreas:	n/a
19	chr1:246457244-246457294	PFSK-1	brain:	n/a
20	chr1:246457244-246457294	NHBE	bronchial:	n/a
21	chr1:246457244-246457294	Hepatocyte	liver:	n/a
22	chr1:246466280-246466330	GM12892	blood:	n/a
23	chr1:246466280-246466330	T-47D	breast:	n/a
24	chr1:246457244-246457294	GM06990	blood:	n/a
25	chr1:246457244-246457294	AG09309	skin:	n/a
26	chr1:246457244-246457294	SKMC	muscle:	n/a
27	chr1:246457244-246457294	HUVEC	blood vessel:	n/a
28	chr1:246466280-246466330	Jurkat	blood:	n/a
29	chr1:246466280-246466330	AG09309	skin:	n/a
30	chr1:246466280-246466330	HAEpiC	amniotic membrane:	n/a
31	chr1:246466280-246466330	NB4	blood:	n/a
32	chr1:246457244-246457294	RPTEC	kidney:	n/a
33	chr1:246466280-246466330	Hepatocyte	liver:	n/a
34	chr1:246466280-246466330	K562	blood:	n/a
35	chr1:246466280-246466330	MCF-7	breast:	n/a
36	chr1:246457244-246457294	IMR90	lung:	fetal
37	chr1:246466280-246466330	HRPEpiC	eye:	n/a
38	chr1:246466280-246466330	GM12878	blood:	n/a
39	chr1:246466280-246466330	SK-N-MC	brain:	n/a
40	chr1:246457244-246457294	GM12892	blood:	n/a
41	chr1:246457244-246457294	CMK	blood:	n/a
42	chr1:246457244-246457294	SK-N-MC	brain:	n/a
43	chr1:246457244-246457294	HAEpiC	amniotic membrane:	n/a
44	chr1:246466280-246466330	HPAEpiC	pulmonary alveolar:	n/a
45	chr1:246457244-246457294	A549	lung:	n/a
46	chr1:246466280-246466330	HCPEpiC	choroid plexus:	n/a
47	chr1:246457244-246457294	HPAEpiC	pulmonary alveolar:	n/a
48	chr1:246457244-246457294	AG09319	gingival:	n/a
49	chr1:246466280-246466330	ECC-1	luminal epithelium:	n/a
50	chr1:246457244-246457294	Caco-2	colon:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:246151420..246154131-chr1:246468233..246469966,2	K562	blood:
2	chr1:246463275..246466123-chr1:246471236..246474164,2	MCF-7	breast:
3	chr1:246478448..246480701-chr1:246489976..246492079,2	MCF-7	breast:
4	chr1:246477291..246479573-chr1:246484385..246486637,2	K562	blood:
5	chr1:246464800..246467604-chr1:246470299..246472286,2	MCF-7	breast:
6	chr1:246478448..246480701-chr1:246489976..246492079,2	MCF-7	breast:
7	chr1:246452108..246454615-chr1:246458116..246460010,2	K562	blood:
8	chr1:246482242..246483844-chr1:246486769..246488361,2	MCF-7	breast:
9	chr1:246451778..246454398-chr1:246470226..246471898,2	K562	blood:
10	chr1:246470110..246471825-chr1:246585890..246587442,2	K562	blood:
11	chr1:246471340..246473899-chr1:246474297..246475919,2	K562	blood:
12	chr1:246497788..246499304-chr1:246499416..246501844,2	MCF-7	breast:
13	chr1:246497788..246499304-chr1:246499416..246501844,2	MCF-7	breast:
14	chr1:246482654..246484211-chr1:246484942..246487391,2	MCF-7	breast:
15	chr1:246463275..246466123-chr1:246471236..246474164,2	MCF-7	breast:
16	chr1:246458189..246460474-chr1:246462017..246465759,3	K562	blood:
17	chr1:246464800..246467604-chr1:246470299..246472286,2	MCF-7	breast:
18	chr1:246482242..246483844-chr1:246486769..246488361,2	MCF-7	breast:
19	chr1:246458189..246460474-chr1:246462017..246465759,3	K562	blood:
20	chr1:246489256..246490981-chr1:246569694..246571729,2	K562	blood:
21	chr1:246471340..246473899-chr1:246474297..246475919,2	K562	blood:
22	chr1:246480625..246484494-chr1:246484509..246487913,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TFB2M-2	chr1:246485586-246485740	ENSG00000230184.1
2	lnc-TFB2M-2	chr1:246484965-246485170	ENSG00000230184.1

No data

Variant related genes	Relation type
SMYD3	TF binding region
SMYD3-IT1	TF binding region
SMYD3	CpG island
SMYD3-IT1	CpG island
ENSG00000230184	chromatin interactions
ENSG00000185420	chromatin interactions

Extended variants
information (count: 1649 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1649 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7516664	chr1:246457214-246457215	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547838853	chr1:246457215-246457216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568153091	chr1:246457224-246457225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184568732	chr1:246457234-246457235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553646007	chr1:246457235-246457236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567046409	chr1:246457252-246457253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539204989	chr1:246457259-246457260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs79850328	chr1:246457277-246457278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs189286395	chr1:246457295-246457296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs145048264	chr1:246457322-246457323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192435699	chr1:246457326-246457327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535663125	chr1:246457364-246457365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs138730263	chr1:246457478-246457479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs554136608	chr1:246457520-246457521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs114370208	chr1:246457529-246457530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs540312645	chr1:246457531-246457532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572735284	chr1:246457586-246457587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555960436	chr1:246457588-246457589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs149343198	chr1:246457614-246457615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545561704	chr1:246457650-246457651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558291699	chr1:246457655-246457656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs377028838	chr1:246457732-246457733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184849387	chr1:246457736-246457737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76565270	chr1:246457767-246457768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs114822875	chr1:246457817-246457818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527419930	chr1:246457885-246457886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533025246	chr1:246457907-246457908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs34272512	chr1:246457908-246457909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs397813388	chr1:246457917-246457918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs75972363	chr1:246457920-246457921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547534906	chr1:246457940-246457941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs570524495	chr1:246457951-246457952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs188748708	chr1:246457970-246457971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs552447433	chr1:246457987-246457988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569580464	chr1:246458010-246458011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1197643	chr1:246458020-246458021	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs554982651	chr1:246458023-246458024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1197644	chr1:246458031-246458032	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs533905934	chr1:246458041-246458042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181574051	chr1:246458118-246458119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1197645	chr1:246458143-246458144	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs545983627	chr1:246458170-246458171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555245469	chr1:246458190-246458191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs111597113	chr1:246458191-246458192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs576328912	chr1:246458196-246458197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541744524	chr1:246458270-246458271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs12040346	chr1:246458351-246458352	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs527295832	chr1:246458356-246458357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547374553	chr1:246458370-246458371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs534555457	chr1:246458441-246458442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	20729466	CNVD
Testicular germ cell tumor	18059402	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD
Schizophrenia	20967226	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	19805367	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:421 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246423400-246509000	Weak transcription	Aorta	Aorta
2	chr1:246435400-246460200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:246441800-246506600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr1:246442600-246460400	Weak transcription	Osteobl	bone
5	chr1:246443200-246469000	Weak transcription	Primary hematopoietic stem cells	blood
6	chr1:246447600-246459000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr1:246447600-246482400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr1:246447600-246502800	Weak transcription	Left Ventricle	heart
9	chr1:246452000-246458800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:246452000-246465200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr1:246454800-246458600	Weak transcription	Brain Germinal Matrix	brain
12	chr1:246455000-246463600	Weak transcription	Fetal Kidney	kidney
13	chr1:246455000-246493000	Weak transcription	Primary B cells from cord blood	blood
14	chr1:246456000-246457400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr1:246456600-246458400	Weak transcription	HUVEC	blood vessel
16	chr1:246456800-246466000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr1:246457000-246458400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr1:246457200-246457600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr1:246457200-246470000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr1:246457800-246458000	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr1:246458000-246459000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr1:246458400-246460000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr1:246458400-246461200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr1:246458400-246461600	Enhancers	HUVEC	blood vessel
25	chr1:246458600-246459200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr1:246458600-246461400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr1:246458800-246461400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr1:246459000-246460800	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr1:246459000-246460800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr1:246459000-246461400	Enhancers	NHEK	skin
31	chr1:246459200-246459600	Enhancers	Fetal Lung	lung
32	chr1:246459200-246459600	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr1:246459200-246459800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr1:246459200-246459800	Enhancers	HSMMtube	muscle
35	chr1:246459200-246460000	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr1:246459200-246460800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr1:246459200-246460800	Enhancers	NH-A	brain
38	chr1:246459200-246461400	Enhancers	HMEC	breast
39	chr1:246459400-246460400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr1:246459400-246464000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr1:246459600-246463800	Weak transcription	Fetal Lung	lung
42	chr1:246459800-246460200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr1:246459800-246465200	Weak transcription	HSMMtube	muscle
44	chr1:246460000-246460400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr1:246460000-246460400	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr1:246460200-246460800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr1:246460200-246460800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr1:246460200-246461000	Enhancers	A549	lung
49	chr1:246460400-246460800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr1:246460400-246460800	Enhancers	Primary monocytes fromperipheralblood	blood

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