Variant report

Variant	nsv549179
Chromosome Location	chr1:213641943-213674732
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:101)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:101 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:213665544-213666001	HepG2	liver:	n/a	n/a
2	CEBPB	chr1:213667284-213667540	IMR90	lung:	n/a	chr1:213667420-213667431
3	CEBPB	chr1:213643324-213643616	K562	blood:	n/a	chr1:213643462-213643473
4	CEBPB	chr1:213643329-213643653	IMR90	lung:	n/a	chr1:213643462-213643473
5	CEBPB	chr1:213646399-213646564	K562	blood:	n/a	chr1:213646475-213646486
6	CEBPB	chr1:213646330-213646654	HepG2	liver:	n/a	chr1:213646475-213646486
7	CEBPB	chr1:213672652-213672757	A549	lung:	n/a	n/a
8	CEBPB	chr1:213643308-213643642	HepG2	liver:	n/a	chr1:213643462-213643473
9	CEBPB	chr1:213667255-213667553	HepG2	liver:	n/a	chr1:213667420-213667431
10	CEBPB	chr1:213672642-213672820	HepG2	liver:	n/a	n/a
11	CEBPB	chr1:213667357-213667506	K562	blood:	n/a	chr1:213667420-213667431
12	CEBPB	chr1:213643318-213643652	A549	lung:	n/a	chr1:213643462-213643473
13	CHD2	chr1:213665562-213665790	HepG2	liver:	n/a	n/a
14	CTCF	chr1:213665620-213665770	HepG2	liver:	n/a	n/a
15	CTCF	chr1:213656613-213656637	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr1:213656596-213656597	Kidney_OC	kidney:	n/a	n/a
17	CTCF	chr1:213647420-213647570	HepG2	liver:	n/a	n/a
18	CTCF	chr1:213665600-213665750	HepG2	liver:	n/a	n/a
19	CTCF	chr1:213647360-213647510	BE2_C	brain:	n/a	n/a
20	EP300	chr1:213665163-213666164	HepG2	liver:	n/a	n/a
21	EP300	chr1:213665519-213666046	HepG2	liver:	n/a	n/a
22	EP300	chr1:213665465-213665986	HepG2	liver:	n/a	n/a
23	FOS	chr1:213657827-213657975	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr1:213657754-213658083	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr1:213656737-213657001	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr1:213669649-213670010	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr1:213656752-213656952	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr1:213670320-213670561	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr1:213669649-213670009	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr1:213669772-213669985	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr1:213672399-213672462	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr1:213669595-213669977	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr1:213656781-213656873	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr1:213656734-213656958	MCF10A-Er-Src	breast:	n/a	n/a
35	FOXA1	chr1:213665400-213666037	HepG2	liver:	n/a	n/a
36	FOXA1	chr1:213665400-213666050	HepG2	liver:	n/a	n/a
37	FOXA1	chr1:213665470-213666005	HepG2	liver:	n/a	n/a
38	FOXA1	chr1:213665425-213666011	HepG2	liver:	n/a	n/a
39	FOXA2	chr1:213667245-213667446	HepG2	liver:	n/a	n/a
40	FOXA2	chr1:213665514-213666035	HepG2	liver:	n/a	n/a
41	FOXA2	chr1:213665268-213666168	HepG2	liver:	n/a	n/a
42	GATA3	chr1:213650092-213650160	SH-SY5Y	brain:	n/a	n/a
43	HDAC2	chr1:213665481-213665947	HepG2	liver:	n/a	n/a
44	HDAC2	chr1:213665407-213666077	HepG2	liver:	n/a	n/a
45	HEY1	chr1:213665472-213665709	HepG2	liver:	n/a	n/a
46	HNF4A	chr1:213665589-213665863	HepG2	liver:	n/a	n/a
47	HNF4G	chr1:213665477-213665878	HepG2	liver:	n/a	n/a
48	JUND	chr1:213659842-213660135	HepG2	liver:	n/a	chr1:213660003-213660012
49	JUND	chr1:213669765-213669865	K562	blood:	n/a	n/a
50	MAFF	chr1:213654759-213655119	HepG2	liver:	n/a	chr1:213654931-213654949

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:213646397-213646447	Jurkat	blood:	n/a
2	chr1:213646397-213646447	MCF10A-Er-Src	breast:	n/a
3	chr1:213646397-213646447	GM12878	blood:	n/a
4	chr1:213646397-213646447	HAEpiC	amniotic membrane:	n/a
5	chr1:213646397-213646447	IMR90	lung:	fetal
6	chr1:213646397-213646447	HPAEpiC	pulmonary alveolar:	n/a
7	chr1:213646397-213646447	GM06990	blood:	n/a
8	chr1:213646397-213646447	HCT-116	colon:	n/a
9	chr1:213646397-213646447	SKMC	muscle:	n/a
10	chr1:213646397-213646447	HIPEpiC	eye:	n/a
11	chr1:213646397-213646447	SK-N-MC	brain:	n/a
12	chr1:213646397-213646447	HCM	heart:	n/a
13	chr1:213646397-213646447	A549	lung:	n/a
14	chr1:213646397-213646447	ProgFib	skin:	n/a
15	chr1:213646397-213646447	LNCaP	prostate:	n/a
16	chr1:213646397-213646447	RPTEC	kidney:	n/a
17	chr1:213646397-213646447	PrEC	prostate:	n/a
18	chr1:213646397-213646447	SK-N-SH	brain:	n/a
19	chr1:213646397-213646447	HCPEpiC	choroid plexus:	n/a
20	chr1:213646397-213646447	Caco-2	colon:	n/a
21	chr1:213646397-213646447	HNPCEpiC	eye:	n/a
22	chr1:213646397-213646447	K562	blood:	n/a
23	chr1:213646397-213646447	ovcar-3	ovarian:	n/a
24	chr1:213646397-213646447	HUVEC	blood vessel:	n/a
25	chr1:213646397-213646447	NHDF-neo	bronchial:	n/a
26	chr1:213646397-213646447	GM19239	blood:	n/a
27	chr1:213646397-213646447	AG10803	skin:	n/a
28	chr1:213646397-213646447	Hepatocyte	liver:	n/a
29	chr1:213646397-213646447	HRPEpiC	eye:	n/a
30	chr1:213646397-213646447	PFSK-1	brain:	n/a
31	chr1:213646397-213646447	MCF-7	breast:	n/a
32	chr1:213646397-213646447	PANC-1	pancreas:	n/a
33	chr1:213646397-213646447	T-47D	breast:	n/a
34	chr1:213646397-213646447	SAEC	small airway:	n/a
35	chr1:213646397-213646447	AG04449	skin:	fetal
36	chr1:213646397-213646447	GM12891	blood:	n/a
37	chr1:213646397-213646447	HCF	heart:	n/a
38	chr1:213646397-213646447	HRCEpiC	kidney:	n/a
39	chr1:213646397-213646447	HMEC	breast:	n/a
40	chr1:213646397-213646447	AoSMC	blood vessel:	n/a
41	chr1:213646397-213646447	SK-N-SH_RA	brain:	n/a
42	chr1:213646397-213646447	AG04450	lung:	fetal
43	chr1:213646397-213646447	NT2-D1	testis:	n/a
44	chr1:213646397-213646447	BJ	skin:	n/a
45	chr1:213646397-213646447	AG09309	skin:	n/a
46	chr1:213646397-213646447	H1-hESC	embryonic stem cell:	embryo
47	chr1:213646397-213646447	HEK293	kidney:	embryo
48	chr1:213646397-213646447	AG09319	gingival:	n/a
49	chr1:213646397-213646447	NH-A	brain:	n/a
50	chr1:213646397-213646447	ECC-1	luminal epithelium:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:213662347..213664389-chr1:213667311..213670072,2	MCF-7	breast:
2	chr1:213640416..213642930-chr1:213643053..213645178,3	K562	blood:
3	chr1:213673826..213676574-chr1:213678134..213680057,2	K562	blood:
4	chr1:213662347..213664389-chr1:213667311..213670072,2	MCF-7	breast:
5	chr1:213640416..213642930-chr1:213643053..213645178,3	K562	blood:
6	chr1:213637145..213640058-chr1:213641140..213642890,2	K562	blood:
7	chr1:213660245..213663549-chr1:213664532..213668464,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPS6KC1-1	chr1:213665644-213665918	XLOC_000557

No data

Variant related genes	Relation type
ENSG00000225233	TF binding region
ENSG00000225233	CpG island
ENSG00000225233	chromatin interactions

Extended variants
information (count: 641 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:641 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs320480	chr1:213641943-213641944	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs572675601	chr1:213641962-213641963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528158319	chr1:213642022-213642023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368024940	chr1:213642113-213642114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs564756735	chr1:213642146-213642147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192230634	chr1:213642160-213642161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs75429473	chr1:213642161-213642162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182804217	chr1:213642249-213642250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141797648	chr1:213642262-213642263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs150429074	chr1:213642328-213642329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115695794	chr1:213642338-213642339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187921238	chr1:213642340-213642341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs145250641	chr1:213642355-213642356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569874290	chr1:213642370-213642371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs117116445	chr1:213642403-213642404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs320481	chr1:213642464-213642465	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs544792098	chr1:213642484-213642485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149128079	chr1:213642501-213642502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568632968	chr1:213642563-213642564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531157397	chr1:213642573-213642574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs193109700	chr1:213642611-213642612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs185501141	chr1:213642680-213642681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143246622	chr1:213642716-213642717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551300078	chr1:213642730-213642731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558294312	chr1:213642760-213642761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576671590	chr1:213642762-213642763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs544045666	chr1:213642823-213642824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs556799847	chr1:213642935-213642936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138744185	chr1:213642955-213642956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573967816	chr1:213642961-213642962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189261413	chr1:213642974-213642975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571118777	chr1:213642979-213642980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539858448	chr1:213642990-213642991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544819080	chr1:213642994-213642995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs66535282	chr1:213643044-213643045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs35329142	chr1:213643046-213643047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs397786148	chr1:213643050-213643051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563457851	chr1:213643066-213643067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs145597416	chr1:213643083-213643084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs116342880	chr1:213643131-213643132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192599742	chr1:213643167-213643168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184305674	chr1:213643193-213643194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546748151	chr1:213643196-213643197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188597184	chr1:213643241-213643242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538693750	chr1:213643271-213643272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181759516	chr1:213643311-213643312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570225974	chr1:213643322-213643323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537384261	chr1:213643329-213643330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138014255	chr1:213643337-213643338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573724879	chr1:213643343-213643344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	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
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	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
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
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	17060936	CNVD
Atypical hemolytic uremic syndrome	19861685	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:213640000-213649200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:213645200-213645400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr1:213645200-213645800	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr1:213645200-213645800	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr1:213645200-213646400	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr1:213645400-213646400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr1:213645400-213646400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr1:213645800-213646000	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr1:213645800-213646000	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr1:213645800-213646600	Enhancers	HepG2	liver
11	chr1:213645800-213647200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr1:213645800-213649800	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr1:213646200-213646800	Enhancers	Fetal Heart	heart
14	chr1:213646200-213647200	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr1:213646200-213647200	Weak transcription	Fetal Muscle Leg	muscle
16	chr1:213646400-213647200	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr1:213646400-213647400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr1:213646400-213647400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr1:213646600-213647200	Weak transcription	HepG2	liver
20	chr1:213646600-213648000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr1:213646800-213647000	Flanking Active TSS	Fetal Heart	heart
22	chr1:213646800-213648000	Enhancers	Right Ventricle	heart
23	chr1:213647000-213647200	Enhancers	Fetal Heart	heart
24	chr1:213647200-213647400	Flanking Active TSS	Fetal Heart	heart
25	chr1:213647200-213647400	Enhancers	HepG2	liver
26	chr1:213647200-213647600	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr1:213647200-213647600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr1:213647200-213647600	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr1:213647200-213647600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr1:213647200-213647600	Enhancers	Psoas Muscle	Psoas
31	chr1:213647200-213647800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr1:213647200-213647800	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr1:213647200-213647800	Enhancers	Fetal Lung	lung
34	chr1:213647200-213647800	Enhancers	Left Ventricle	heart
35	chr1:213647200-213647800	Enhancers	Ovary	ovary
36	chr1:213647200-213647800	Enhancers	Pancreas	Pancrea
37	chr1:213647200-213647800	Enhancers	Right Atrium	heart
38	chr1:213647200-213648000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr1:213647200-213648800	Enhancers	Fetal Muscle Leg	muscle
40	chr1:213647400-213647600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr1:213647400-213647800	Enhancers	Brain Anterior Caudate	brain
42	chr1:213647400-213647800	Enhancers	Fetal Muscle Trunk	muscle
43	chr1:213647400-213647800	Flanking Active TSS	HepG2	liver
44	chr1:213647400-213650200	Enhancers	Fetal Heart	heart
45	chr1:213647800-213648000	Enhancers	HepG2	liver
46	chr1:213647800-213649200	Weak transcription	Fetal Muscle Trunk	muscle
47	chr1:213648200-213648600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr1:213649200-213649600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr1:213649200-213649600	Enhancers	Fetal Muscle Trunk	muscle
50	chr1:213649200-213650600	Enhancers	Placenta Amnion	Placenta Amnion

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