Variant report

Variant	nsv560038
Chromosome Location	chr12:104053420-104092996
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:132)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:132 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:104066332-104066931	HepG2	liver:	n/a	n/a
2	ATF1	chr12:104074575-104074806	K562	blood:	n/a	n/a
3	BATF	chr12:104082548-104082857	GM12878	blood:	n/a	n/a
4	BATF	chr12:104092561-104092906	GM12878	blood:	n/a	n/a
5	BCL3	chr12:104079106-104079364	GM12878	blood:	n/a	n/a
6	BHLHE40	chr12:104074439-104074809	K562	blood:	n/a	n/a
7	CCNT2	chr12:104074480-104074916	K562	blood:	n/a	n/a
8	CEBPB	chr12:104092648-104092733	A549	lung:	n/a	n/a
9	CEBPB	chr12:104066465-104067034	A549	lung:	n/a	n/a
10	CEBPB	chr12:104060730-104060802	A549	lung:	n/a	chr12:104060750-104060759 chr12:104060748-104060761
11	CEBPB	chr12:104073820-104074029	HepG2	liver:	n/a	n/a
12	CEBPB	chr12:104074525-104074832	K562	blood:	n/a	n/a
13	CEBPB	chr12:104066580-104066895	A549	lung:	n/a	n/a
14	CEBPB	chr12:104066590-104066800	HepG2	liver:	n/a	n/a
15	CEBPB	chr12:104065637-104065669	HepG2	liver:	n/a	n/a
16	CEBPB	chr12:104066532-104066907	HepG2	liver:	n/a	n/a
17	CEBPB	chr12:104073906-104073971	IMR90	lung:	n/a	n/a
18	CEBPB	chr12:104066581-104066885	A549	lung:	n/a	n/a
19	CEBPD	chr12:104074446-104074808	K562	blood:	n/a	n/a
20	CEBPD	chr12:104074449-104074908	K562	blood:	n/a	n/a
21	CHD2	chr12:104092813-104092928	GM12878	blood:	n/a	n/a
22	CREB1	chr12:104074390-104074830	K562	blood:	n/a	n/a
23	CTCF	chr12:104080560-104080710	GM12865	blood:	n/a	n/a
24	CTCF	chr12:104062360-104062510	GM12868	blood:	n/a	n/a
25	CTCF	chr12:104067885-104068007	HepG2	liver:	n/a	n/a
26	CTCF	chr12:104089440-104089590	GM12871	blood:	n/a	n/a
27	CTCF	chr12:104079230-104079270	MCF-7	breast:	n/a	n/a
28	CTCF	chr12:104062580-104062730	GM12869	blood:	n/a	n/a
29	CTCF	chr12:104079860-104080010	K562	blood:	n/a	n/a
30	CTCF	chr12:104067840-104067990	HepG2	liver:	n/a	n/a
31	CTCF	chr12:104081787-104081831	Fibrobl	skin:	n/a	n/a
32	CTCF	chr12:104062320-104062470	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr12:104062380-104062530	GM12865	blood:	n/a	n/a
34	E2F4	chr12:104059057-104059192	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr12:104068898-104068905	MCF10A-Er-Src	breast:	n/a	n/a
36	EBF1	chr12:104092680-104092716	GM12878	blood:	n/a	n/a
37	EGR1	chr12:104074502-104074874	K562	blood:	n/a	chr12:104074685-104074700
38	EGR1	chr12:104074549-104074778	K562	blood:	n/a	chr12:104074685-104074700
39	EP300	chr12:104092680-104092928	GM12878	blood:	n/a	n/a
40	EP300	chr12:104066297-104066802	HepG2	liver:	n/a	n/a
41	EP300	chr12:104074349-104074712	SK-N-SH_RA	brain:	n/a	n/a
42	EP300	chr12:104073971-104075407	SK-N-SH	brain:	n/a	chr12:104075070-104075084
43	EP300	chr12:104074714-104074768	GM12878	blood:	n/a	n/a
44	EP300	chr12:104074398-104074780	SK-N-SH_RA	brain:	n/a	n/a
45	EP300	chr12:104092618-104092918	GM12878	blood:	n/a	n/a
46	EP300	chr12:104074661-104074724	GM12878	blood:	n/a	n/a
47	FOS	chr12:104082261-104082338	MCF10A-Er-Src	breast:	n/a	chr12:104082292-104082300 chr12:104082292-104082301 chr12:104082292-104082299
48	FOSL2	chr12:104067731-104068029	HepG2	liver:	n/a	chr12:104067896-104067908 chr12:104067897-104067907 chr12:104067898-104067906 chr12:104067898-104067906 chr12:104067894-104067905 chr12:104067899-104067906
49	FOSL2	chr12:104066301-104066827	A549	lung:	n/a	n/a
50	FOXA1	chr12:104084217-104084485	T-47D	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:104063640-104063690	Hela-S3	cervix:	n/a
2	chr12:104063640-104063690	ovcar-3	ovarian:	n/a
3	chr12:104063640-104063690	MCF10A-Er-Src	breast:	n/a
4	chr12:104063640-104063690	SK-N-SH_RA	brain:	n/a
5	chr12:104063640-104063690	K562	blood:	n/a
6	chr12:104063640-104063690	BJ	skin:	n/a
7	chr12:104063640-104063690	PANC-1	pancreas:	n/a
8	chr12:104063640-104063690	HUVEC	blood vessel:	n/a
9	chr12:104063640-104063690	NHDF-neo	bronchial:	n/a
10	chr12:104063640-104063690	GM12892	blood:	n/a
11	chr12:104063640-104063690	NT2-D1	testis:	n/a
12	chr12:104063640-104063690	HNPCEpiC	eye:	n/a
13	chr12:104063640-104063690	HRCEpiC	kidney:	n/a
14	chr12:104063640-104063690	HRPEpiC	eye:	n/a
15	chr12:104063640-104063690	AG04450	lung:	fetal
16	chr12:104063640-104063690	HCT-116	colon:	n/a
17	chr12:104063640-104063690	SK-N-SH	brain:	n/a
18	chr12:104063640-104063690	HCPEpiC	choroid plexus:	n/a
19	chr12:104063640-104063690	AG09319	gingival:	n/a
20	chr12:104063640-104063690	BE2_C	brain:	n/a
21	chr12:104063640-104063690	Jurkat	blood:	n/a
22	chr12:104063640-104063690	A549	lung:	n/a
23	chr12:104063640-104063690	LNCaP	prostate:	n/a
24	chr12:104063640-104063690	Caco-2	colon:	n/a
25	chr12:104063640-104063690	ECC-1	luminal epithelium:	n/a
26	chr12:104063640-104063690	GM06990	blood:	n/a
27	chr12:104063640-104063690	Hepatocyte	liver:	n/a
28	chr12:104063640-104063690	NH-A	brain:	n/a
29	chr12:104063640-104063690	HCF	heart:	n/a
30	chr12:104063640-104063690	NHBE	bronchial:	n/a
31	chr12:104063640-104063690	H1-hESC	embryonic stem cell:	embryo
32	chr12:104063640-104063690	HEK293	kidney:	embryo
33	chr12:104063640-104063690	HepG2	liver:	n/a
34	chr12:104063640-104063690	HRE	kidney:	n/a
35	chr12:104063640-104063690	CMK	blood:	n/a
36	chr12:104063640-104063690	MCF-7	breast:	n/a
37	chr12:104063640-104063690	AG10803	skin:	n/a
38	chr12:104063640-104063690	GM19239	blood:	n/a
39	chr12:104063640-104063690	U87	brain:	n/a
40	chr12:104063640-104063690	T-47D	breast:	n/a
41	chr12:104063640-104063690	RPTEC	kidney:	n/a
42	chr12:104063640-104063690	PrEC	prostate:	n/a
43	chr12:104063640-104063690	PFSK-1	brain:	n/a
44	chr12:104063640-104063690	GM12891	blood:	n/a
45	chr12:104063640-104063690	HIPEpiC	eye:	n/a
46	chr12:104063640-104063690	HPAEpiC	pulmonary alveolar:	n/a
47	chr12:104063640-104063690	SKMC	muscle:	n/a
48	chr12:104063640-104063690	HMEC	breast:	n/a
49	chr12:104063640-104063690	SK-N-MC	brain:	n/a
50	chr12:104063640-104063690	HAEpiC	amniotic membrane:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:104078901..104081759-chr12:104083447..104084951,2	K562	blood:
2	chr12:104086671..104088955-chr12:104090916..104093628,2	K562	blood:
3	chr12:104054220..104056283-chr12:104057216..104059364,2	K562	blood:
4	chr12:104088458..104089096-chr15:42219142..42219833,2	MCF-7	breast:
5	chr12:104058121..104061173-chr12:104061276..104064386,3	K562	blood:
6	chr12:104054220..104056283-chr12:104057216..104059364,2	K562	blood:
7	chr12:104089001..104091974-chr12:104092172..104093862,2	MCF-7	breast:
8	chr12:104078901..104081759-chr12:104083447..104084951,2	K562	blood:
9	chr12:104086671..104088955-chr12:104090916..104093628,2	K562	blood:
10	chr12:104056086..104059213-chr12:104060353..104063623,3	K562	blood:
11	chr12:104089001..104091974-chr12:104092172..104093862,2	MCF-7	breast:
12	chr12:104083131..104086634-chr12:104100457..104102574,3	K562	blood:
13	chr12:104082267..104084124-chr12:104087280..104090168,2	K562	blood:
14	chr12:104082267..104084124-chr12:104087280..104090168,2	K562	blood:
15	chr12:104061705..104063209-chr12:104063963..104066627,2	MCF-7	breast:
16	chr12:104083504..104086634-chr12:104099409..104102574,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NT5DC3-2	chr12:104062990-104063184	ENSG00000257766.1
2	lnc-NT5DC3-2	chr12:104062353-104062625	ENSG00000257766.1
3	lnc-RP11-650K20.3.1-4	chr12:104066248-104066547	expReg_chr12_9712_+

No data

Variant related genes	Relation type
ENSG00000257766	TF binding region
STAB2	TF binding region
ENSG00000257737	TF binding region
ENSG00000257766	CpG island
STAB2	CpG island
ENSG00000257737	CpG island
ENSG00000257766	chromatin interactions

Extended variants
information (count: 1777 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1777 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7315384	chr12:104053420-104053421	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536073917	chr12:104053462-104053463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371549700	chr12:104053470-104053471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566475639	chr12:104053477-104053478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374225693	chr12:104053486-104053487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558174737	chr12:104053554-104053555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368596173	chr12:104053595-104053596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375563717	chr12:104053596-104053597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542382183	chr12:104053602-104053603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs80011491	chr12:104053604-104053605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534726504	chr12:104053651-104053652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192337850	chr12:104053719-104053720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs149904111	chr12:104053738-104053739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs527966489	chr12:104053770-104053771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560630812	chr12:104053847-104053848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144961818	chr12:104053872-104053873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs376965247	chr12:104053898-104053899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551141261	chr12:104053915-104053916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs142910949	chr12:104053918-104053919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546287515	chr12:104053922-104053923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183660091	chr12:104053931-104053932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs11111705	chr12:104053955-104053956	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs527347350	chr12:104053996-104053997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs80324563	chr12:104054029-104054030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112102449	chr12:104054030-104054031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs145915437	chr12:104054052-104054053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377249394	chr12:104054066-104054067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372552200	chr12:104054116-104054117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188061929	chr12:104054133-104054134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141698852	chr12:104054146-104054147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538317123	chr12:104054165-104054166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551872986	chr12:104054192-104054193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568476680	chr12:104054196-104054197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192270068	chr12:104054202-104054203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76063084	chr12:104054240-104054241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368024484	chr12:104054270-104054271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531550349	chr12:104054299-104054300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575075811	chr12:104054301-104054302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35871284	chr12:104054343-104054344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376086874	chr12:104054415-104054416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200938200	chr12:104054416-104054417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs831427	chr12:104054434-104054435	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs374848555	chr12:104054447-104054448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568506711	chr12:104054457-104054458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200307097	chr12:104054472-104054473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150542482	chr12:104054486-104054487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138849911	chr12:104054503-104054504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562986267	chr12:104054513-104054514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368992908	chr12:104054515-104054516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373309541	chr12:104054526-104054527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	22032731	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
lymphocytic leukemia	21291569	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Neurocytoma	17123091	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:249 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:104033200-104062200	Weak transcription	Spleen	Spleen
2	chr12:104047000-104059400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr12:104052200-104059200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr12:104059200-104059800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr12:104059200-104060000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr12:104059200-104060200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:104059200-104061600	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr12:104059400-104060200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr12:104059600-104059800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr12:104059600-104060000	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr12:104059600-104060200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr12:104059600-104060200	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr12:104059600-104060200	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr12:104059600-104060200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr12:104059600-104060200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr12:104059600-104060400	Enhancers	H9 Cell Line	embryonic stem cell
17	chr12:104059800-104060000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr12:104059800-104060200	Enhancers	H1 Cell Line	embryonic stem cell
19	chr12:104060000-104060200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
20	chr12:104060000-104063400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr12:104060000-104063600	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr12:104060000-104064000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr12:104060200-104061600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr12:104060200-104063000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr12:104060200-104063000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr12:104060200-104063200	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr12:104060200-104063200	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr12:104060200-104063200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr12:104060200-104063600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr12:104060400-104060800	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr12:104060800-104061400	Enhancers	H9 Cell Line	embryonic stem cell
32	chr12:104061000-104061400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr12:104061000-104061600	Enhancers	Fetal Heart	heart
34	chr12:104061400-104063200	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr12:104061600-104064000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr12:104062200-104062600	Genic enhancers	Spleen	Spleen
37	chr12:104062200-104063400	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr12:104062600-104063000	Strong transcription	Spleen	Spleen
39	chr12:104063000-104063200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr12:104063000-104064800	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr12:104063000-104067400	Weak transcription	Spleen	Spleen
42	chr12:104063200-104063400	Enhancers	H1 Cell Line	embryonic stem cell
43	chr12:104063200-104063600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr12:104063200-104064200	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr12:104063200-104064600	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr12:104063200-104064800	Enhancers	H9 Cell Line	embryonic stem cell
47	chr12:104063200-104064800	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr12:104063400-104063600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
49	chr12:104063400-104064000	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr12:104063400-104064400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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