Variant report

Variant	nsv873064
Chromosome Location	chr1:197008597-197035538
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:86)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:86 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:197024184-197024295	K562	blood:	n/a	n/a
2	CCNT2	chr1:197011538-197011614	K562	blood:	n/a	n/a
3	CEBPB	chr1:197035462-197035745	HepG2	liver:	n/a	chr1:197035618-197035629 chr1:197035617-197035630 chr1:197035617-197035628
4	CTCF	chr1:197032380-197032530	K562	blood:	n/a	n/a
5	CTCF	chr1:197032480-197032630	Hela-S3	cervix:	n/a	n/a
6	CTCF	chr1:197032440-197032590	HPAF	blood vessel:	n/a	n/a
7	CTCF	chr1:197032400-197032550	A549	lung:	n/a	n/a
8	CTCF	chr1:197032540-197032690	HPAF	blood vessel:	n/a	n/a
9	CTCF	chr1:197032380-197032530	HMF	breast:	n/a	n/a
10	CTCF	chr1:197032340-197032490	HCM	heart:	n/a	n/a
11	CTCF	chr1:197032440-197032590	GM12866	blood:	n/a	n/a
12	CTCF	chr1:197032460-197032610	AG10803	skin:	n/a	n/a
13	CTCF	chr1:197032420-197032570	MCF-7	breast:	n/a	n/a
14	CTCF	chr1:197032480-197032630	HCPEpiC	choroid plexus:	n/a	n/a
15	CTCF	chr1:197032440-197032590	AoAF	blood vessel:	n/a	n/a
16	CTCF	chr1:197014955-197015054	Lung_OC	lung:	n/a	n/a
17	CTCF	chr1:197032480-197032630	MCF-7	breast:	n/a	n/a
18	CTCF	chr1:197032500-197032650	HEK293	kidney:	n/a	n/a
19	CTCF	chr1:197032480-197032630	HBMEC	blood vessel:	n/a	n/a
20	CTCF	chr1:197014954-197015012	GM20000	blood:	n/a	n/a
21	CTCF	chr1:197032440-197032590	HCFaa	heart:	n/a	n/a
22	CTCF	chr1:197032420-197032570	BE2_C	brain:	n/a	n/a
23	CTCF	chr1:197032440-197032590	HEEpiC	esophagus:	n/a	n/a
24	EBF1	chr1:197034879-197034963	GM12878	blood:	n/a	chr1:197034919-197034930
25	EP300	chr1:197028560-197028725	K562	blood:	n/a	n/a
26	EP300	chr1:197012130-197012656	A549	lung:	n/a	n/a
27	FAM48A	chr1:197034924-197035120	GM12878	blood:	n/a	n/a
28	FOSL2	chr1:197012079-197012645	A549	lung:	n/a	n/a
29	FOXA1	chr1:197035462-197035704	HepG2	liver:	n/a	n/a
30	FOXA1	chr1:197012129-197012521	HepG2	liver:	n/a	chr1:197012389-197012404
31	FOXA1	chr1:197012111-197012494	HepG2	liver:	n/a	chr1:197012389-197012404
32	FOXA1	chr1:197012045-197012587	HepG2	liver:	n/a	chr1:197012389-197012404
33	FOXA2	chr1:197011854-197012113	HepG2	liver:	n/a	n/a
34	FOXA2	chr1:197011748-197012676	A549	lung:	n/a	n/a
35	FOXA2	chr1:197012165-197012475	HepG2	liver:	n/a	n/a
36	FOXA2	chr1:197035500-197035752	HepG2	liver:	n/a	n/a
37	GATA3	chr1:197029125-197029656	SK-N-SH	brain:	n/a	chr1:197029448-197029460 chr1:197029446-197029462
38	GATA3	chr1:197017701-197017741	SH-SY5Y	brain:	n/a	n/a
39	GATA3	chr1:197034583-197035103	SK-N-SH	brain:	n/a	n/a
40	GATA3	chr1:197029153-197029768	SK-N-SH	brain:	n/a	chr1:197029448-197029460 chr1:197029446-197029462
41	MAFF	chr1:197013263-197013529	HepG2	liver:	n/a	chr1:197013359-197013377 chr1:197013400-197013418
42	MAFK	chr1:197013353-197013453	IMR90	lung:	n/a	chr1:197013401-197013416 chr1:197013360-197013375
43	MAFK	chr1:197030409-197030597	HepG2	liver:	n/a	chr1:197030481-197030501 chr1:197030483-197030499
44	MAFK	chr1:197018305-197018538	HepG2	liver:	n/a	n/a
45	MAFK	chr1:197018410-197018522	HepG2	liver:	n/a	n/a
46	MAFK	chr1:197033343-197033630	HepG2	liver:	n/a	n/a
47	MAFK	chr1:197018401-197018519	IMR90	lung:	n/a	n/a
48	MAFK	chr1:197026410-197026510	HepG2	liver:	n/a	chr1:197026460-197026475
49	MAFK	chr1:197013220-197013524	HepG2	liver:	n/a	chr1:197013401-197013416 chr1:197013360-197013375
50	MAFK	chr1:197013284-197013504	HepG2	liver:	n/a	chr1:197013401-197013416 chr1:197013360-197013375

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:197030122-197030172	K562	blood:	n/a
2	chr1:197030122-197030172	SAEC	small airway:	n/a
3	chr1:197030122-197030172	HRCEpiC	kidney:	n/a
4	chr1:197030122-197030172	AG10803	skin:	n/a
5	chr1:197030122-197030172	PFSK-1	brain:	n/a
6	chr1:197030122-197030172	SK-N-MC	brain:	n/a
7	chr1:197030122-197030172	CMK	blood:	n/a
8	chr1:197030122-197030172	AoSMC	blood vessel:	n/a
9	chr1:197030122-197030172	HEK293	kidney:	embryo
10	chr1:197030122-197030172	MCF10A-Er-Src	breast:	n/a
11	chr1:197030122-197030172	HNPCEpiC	eye:	n/a
12	chr1:197030122-197030172	SKMC	muscle:	n/a
13	chr1:197030122-197030172	HL-60	blood:	n/a
14	chr1:197030122-197030172	Hepatocyte	liver:	n/a
15	chr1:197030122-197030172	SK-N-SH	brain:	n/a
16	chr1:197030122-197030172	Jurkat	blood:	n/a
17	chr1:197030122-197030172	HCM	heart:	n/a
18	chr1:197030122-197030172	MCF-7	breast:	n/a
19	chr1:197030122-197030172	HRE	kidney:	n/a
20	chr1:197030122-197030172	NB4	blood:	n/a
21	chr1:197030122-197030172	ECC-1	luminal epithelium:	n/a
22	chr1:197030122-197030172	HPAEpiC	pulmonary alveolar:	n/a
23	chr1:197030122-197030172	AG09319	gingival:	n/a
24	chr1:197030122-197030172	AG04449	skin:	fetal
25	chr1:197030122-197030172	GM12878	blood:	n/a
26	chr1:197030122-197030172	ovcar-3	ovarian:	n/a
27	chr1:197030122-197030172	BE2_C	brain:	n/a
28	chr1:197030122-197030172	AG04450	lung:	fetal
29	chr1:197030122-197030172	NT2-D1	testis:	n/a
30	chr1:197030122-197030172	HUVEC	blood vessel:	n/a
31	chr1:197030122-197030172	ProgFib	skin:	n/a
32	chr1:197030122-197030172	H1-hESC	embryonic stem cell:	embryo
33	chr1:197030122-197030172	SK-N-SH_RA	brain:	n/a
34	chr1:197030122-197030172	HCF	heart:	n/a
35	chr1:197030122-197030172	HEEpiC	esophagus:	n/a
36	chr1:197030122-197030172	HCPEpiC	choroid plexus:	n/a
37	chr1:197030122-197030172	GM12891	blood:	n/a
38	chr1:197030122-197030172	NH-A	brain:	n/a
39	chr1:197030122-197030172	GM19239	blood:	n/a
40	chr1:197030122-197030172	HIPEpiC	eye:	n/a
41	chr1:197030122-197030172	AG09309	skin:	n/a
42	chr1:197030122-197030172	Hela-S3	cervix:	n/a
43	chr1:197030122-197030172	IMR90	lung:	fetal
44	chr1:197030122-197030172	BJ	skin:	n/a
45	chr1:197030122-197030172	RPTEC	kidney:	n/a
46	chr1:197030122-197030172	NHDF-neo	bronchial:	n/a
47	chr1:197030122-197030172	NHBE	bronchial:	n/a
48	chr1:197030122-197030172	T-47D	breast:	n/a
49	chr1:197030122-197030172	U87	brain:	n/a
50	chr1:197030122-197030172	GM06990	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:197026462..197029856-chr1:197031681..197034887,3	K562	blood:
2	chr1:197026462..197029856-chr1:197031681..197034887,3	K562	blood:
3	chr1:197017524..197019536-chr1:197026374..197028329,2	K562	blood:
4	chr1:197000503..197002101-chr1:197024032..197026765,2	K562	blood:
5	chr1:197017643..197020218-chr1:197023461..197025203,2	MCF-7	breast:
6	chr1:197017524..197019536-chr1:197026374..197028329,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASPM-2	chr1:197009275-197009507	NONHSAT008610
2	lnc-ASPM-2	chr1:197009652-197009865	NONHSAT008610
3	lnc-ASPM-2	chr1:197019827-197019975	NONHSAT008610

No data

Variant related genes	Relation type
F13B	TF binding region
F13B	CpG island
ENSG00000143278	chromatin interactions

Extended variants
information (count: 1015 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1015 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs5990	chr1:197008597-197008598	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs138524182	chr1:197008629-197008630	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185899062	chr1:197008644-197008645	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs17549866	chr1:197008670-197008671	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs192492875	chr1:197008682-197008683	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555905011	chr1:197008712-197008713	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs17549859	chr1:197008736-197008737	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs550581158	chr1:197008759-197008760	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs17549853	chr1:197008775-197008776	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs556185155	chr1:197008781-197008782	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376291708	chr1:197008872-197008873	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs17514823	chr1:197008879-197008880	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs545700862	chr1:197008917-197008918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs557595844	chr1:197008927-197008928	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573017738	chr1:197008969-197008970	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540083411	chr1:197008983-197008984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560808945	chr1:197009008-197009009	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561905432	chr1:197009012-197009013	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs857024	chr1:197009062-197009063	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs17514816	chr1:197009067-197009068	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs532924362	chr1:197009078-197009079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs17514809	chr1:197009097-197009098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182049759	chr1:197009133-197009134	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs79523613	chr1:197009167-197009168	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs17514802	chr1:197009179-197009180	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs552119829	chr1:197009290-197009291	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs567077766	chr1:197009368-197009369	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs187213551	chr1:197009385-197009386	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs190501839	chr1:197009408-197009409	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs567844667	chr1:197009414-197009415	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs112202513	chr1:197009441-197009442	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs537956552	chr1:197009461-197009462	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs566767094	chr1:197009504-197009505	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs12134960	chr1:197009508-197009509	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs182784658	chr1:197009572-197009573	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369324380	chr1:197009620-197009621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149091258	chr1:197009669-197009670	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs140531979	chr1:197009688-197009689	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs187071483	chr1:197009699-197009700	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs142886126	chr1:197009702-197009703	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs138218533	chr1:197009706-197009707	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs201438197	chr1:197009727-197009728	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs375961962	chr1:197009789-197009790	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs5998	chr1:197009798-197009799	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs544335603	chr1:197009823-197009824	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs368242266	chr1:197009831-197009832	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs147163101	chr1:197009850-197009851	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs556380704	chr1:197009871-197009872	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575018842	chr1:197009881-197009882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111517419	chr1:197009902-197009903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
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
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:197004800-197010600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr1:197005000-197012000	Weak transcription	A549	lung
3	chr1:197008200-197011400	Strong transcription	Liver	Liver
4	chr1:197010600-197010800	Enhancers	GM12878-XiMat	blood
5	chr1:197010600-197011200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr1:197010600-197011600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr1:197010600-197011600	Active TSS	Osteobl	bone
8	chr1:197010800-197011000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr1:197010800-197011200	Enhancers	Dnd41	blood
10	chr1:197010800-197011200	Flanking Active TSS	GM12878-XiMat	blood
11	chr1:197011000-197011200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
12	chr1:197011000-197011400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr1:197011200-197011400	Active TSS	GM12878-XiMat	blood
14	chr1:197011400-197017400	Weak transcription	Liver	Liver
15	chr1:197011800-197012800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr1:197012000-197012400	Active TSS	A549	lung
17	chr1:197012000-197013400	Enhancers	HepG2	liver
18	chr1:197012600-197013000	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr1:197013200-197013600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr1:197017400-197029400	Strong transcription	Liver	Liver
21	chr1:197029400-197029800	Weak transcription	Liver	Liver
22	chr1:197029800-197031000	Genic enhancers	Liver	Liver
23	chr1:197031000-197033000	Enhancers	Liver	Liver
24	chr1:197031200-197032200	Enhancers	GM12878-XiMat	blood
25	chr1:197032000-197032200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr1:197032200-197032400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr1:197032200-197034000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr1:197033000-197034400	Flanking Active TSS	Liver	Liver
29	chr1:197034000-197034400	Enhancers	HSMMtube	muscle
30	chr1:197034000-197035200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr1:197034200-197034800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr1:197034200-197035200	Enhancers	Osteobl	bone
33	chr1:197034200-197035800	Enhancers	Fetal Heart	heart
34	chr1:197034400-197035000	Enhancers	Placenta Amnion	Placenta Amnion
35	chr1:197034400-197036600	Active TSS	Liver	Liver
36	chr1:197034600-197035200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:197035400-197036600	Active TSS	Fetal Intestine Large	intestine

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