Variant report

Variant	esv275028
Chromosome Location	chr1:214637808-214639253
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:23)
CpG islands
(count:184)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:23 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr1:214638004-214638229	K562	blood:	n/a	n/a
2	CBX3	chr1:214637820-214638226	K562	blood:	n/a	n/a
3	CTCF	chr1:214637855-214638246	K562	blood:	n/a	n/a
4	CTCF	chr1:214637905-214638211	K562	blood:	n/a	n/a
5	CTCF	chr1:214638014-214638220	K562	blood:	n/a	n/a
6	CTCF	chr1:214637959-214638302	K562	blood:	n/a	n/a
7	E2F6	chr1:214637873-214638175	K562	blood:	n/a	chr1:214637942-214637951
8	EP300	chr1:214637983-214638076	K562	blood:	n/a	n/a
9	MAX	chr1:214637920-214638148	K562	blood:	n/a	n/a
10	MAX	chr1:214637894-214638147	K562	blood:	n/a	n/a
11	MAX	chr1:214637685-214638293	K562	blood:	n/a	n/a
12	MAZ	chr1:214637861-214638209	K562	blood:	n/a	n/a
13	MYC	chr1:214637906-214637962	K562	blood:	n/a	n/a
14	MYC	chr1:214637832-214638224	K562	blood:	n/a	n/a
15	MYC	chr1:214637889-214638232	K562	blood:	n/a	n/a
16	MYC	chr1:214637971-214638080	K562	blood:	n/a	n/a
17	POLR2A	chr1:214637960-214637973	MCF-7	breast:	n/a	n/a
18	RCOR1	chr1:214637956-214638223	K562	blood:	n/a	n/a
19	REST	chr1:214637975-214638147	K562	blood:	n/a	n/a
20	REST	chr1:214637869-214638213	K562	blood:	n/a	n/a
21	TBL1XR1	chr1:214637979-214638013	K562	blood:	n/a	n/a
22	UBTF	chr1:214637882-214638200	K562	blood:	n/a	n/a
23	ZNF143	chr1:214637993-214638124	K562	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:214638168-214638218	HAEpiC	amniotic membrane:	n/a
2	chr1:214638168-214638218	HAEpiC	amniotic membrane:	n/a
3	chr1:214638070-214638120	AoSMC	blood vessel:	n/a
4	chr1:214638070-214638120	HAEpiC	amniotic membrane:	n/a
5	chr1:214638168-214638218	HUVEC	blood vessel:	n/a
6	chr1:214638168-214638218	MCF10A-Er-Src	breast:	n/a
7	chr1:214638168-214638218	Hepatocyte	liver:	n/a
8	chr1:214637903-214637953	Caco-2	colon:	n/a
9	chr1:214637903-214637953	AG04449	skin:	fetal
10	chr1:214638070-214638120	BE2_C	brain:	n/a
11	chr1:214638168-214638218	PrEC	prostate:	n/a
12	chr1:214637903-214637953	Hela-S3	cervix:	n/a
13	chr1:214638168-214638218	HL-60	blood:	n/a
14	chr1:214638070-214638120	U87	brain:	n/a
15	chr1:214638070-214638120	LNCaP	prostate:	n/a
16	chr1:214638168-214638218	LNCaP	prostate:	n/a
17	chr1:214637903-214637953	IMR90	lung:	fetal
18	chr1:214637903-214637953	HCT-116	colon:	n/a
19	chr1:214637903-214637953	GM12878	blood:	n/a
20	chr1:214638168-214638218	AG04449	skin:	fetal
21	chr1:214638070-214638120	HRCEpiC	kidney:	n/a
22	chr1:214638168-214638218	NHDF-neo	bronchial:	n/a
23	chr1:214638070-214638120	AG09319	gingival:	n/a
24	chr1:214638168-214638218	HRPEpiC	eye:	n/a
25	chr1:214638070-214638120	NHDF-neo	bronchial:	n/a
26	chr1:214637903-214637953	BJ	skin:	n/a
27	chr1:214637903-214637953	ECC-1	luminal epithelium:	n/a
28	chr1:214637903-214637953	AG09309	skin:	n/a
29	chr1:214638168-214638218	H1-hESC	embryonic stem cell:	embryo
30	chr1:214637903-214637953	GM12891	blood:	n/a
31	chr1:214638168-214638218	CMK	blood:	n/a
32	chr1:214637903-214637953	AG09319	gingival:	n/a
33	chr1:214638070-214638120	HUVEC	blood vessel:	n/a
34	chr1:214638168-214638218	AG09309	skin:	n/a
35	chr1:214637903-214637953	HRPEpiC	eye:	n/a
36	chr1:214637903-214637953	NT2-D1	testis:	n/a
37	chr1:214637903-214637953	HRCEpiC	kidney:	n/a
38	chr1:214638168-214638218	AoSMC	blood vessel:	n/a
39	chr1:214638168-214638218	T-47D	breast:	n/a
40	chr1:214638070-214638120	AG09309	skin:	n/a
41	chr1:214637903-214637953	H1-hESC	embryonic stem cell:	embryo
42	chr1:214638070-214638120	T-47D	breast:	n/a
43	chr1:214638168-214638218	GM12878	blood:	n/a
44	chr1:214637903-214637953	PANC-1	pancreas:	n/a
45	chr1:214638070-214638120	HCF	heart:	n/a
46	chr1:214637903-214637953	NHDF-neo	bronchial:	n/a
47	chr1:214638070-214638120	HRPEpiC	eye:	n/a
48	chr1:214637903-214637953	Jurkat	blood:	n/a
49	chr1:214638070-214638120	HCM	heart:	n/a
50	chr1:214638168-214638218	HRCEpiC	kidney:	n/a

No data

Variant related genes	Relation type
PTPN14	TF binding region
PTPN14	CpG island

Extended variants
information (count: 99 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:99 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17733739	chr1:214637808-214637809	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566136017	chr1:214637839-214637840	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs528591378	chr1:214637847-214637848	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs7528315	chr1:214637882-214637883	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs571748820	chr1:214637903-214637904	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs374766505	chr1:214637929-214637930	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs369865001	chr1:214637939-214637940	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs202193414	chr1:214637940-214637941	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs202087037	chr1:214637941-214637942	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs567649634	chr1:214637949-214637950	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs369491846	chr1:214637950-214637951	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs535057324	chr1:214637961-214637962	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs201313994	chr1:214637963-214637964	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs572068380	chr1:214638008-214638009	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs200434667	chr1:214638012-214638013	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs200399097	chr1:214638032-214638033	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs142949490	chr1:214638048-214638049	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs151121546	chr1:214638055-214638056	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs543676404	chr1:214638058-214638059	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs541522296	chr1:214638065-214638066	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs201332095	chr1:214638076-214638077	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs141037132	chr1:214638102-214638103	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs201853931	chr1:214638112-214638113	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs372985987	chr1:214638118-214638119	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs143441007	chr1:214638120-214638121	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs529225480	chr1:214638125-214638126	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs377174915	chr1:214638161-214638162	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs370374002	chr1:214638165-214638166	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs374375933	chr1:214638167-214638168	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs377345250	chr1:214638168-214638169	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs559496857	chr1:214638169-214638170	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs10864100	chr1:214638172-214638173	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs543417066	chr1:214638185-214638186	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs372072155	chr1:214638191-214638192	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs571750329	chr1:214638198-214638199	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs530990938	chr1:214638238-214638239	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs184033306	chr1:214638286-214638287	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs567588499	chr1:214638296-214638297	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs10864101	chr1:214638319-214638320	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs10864102	chr1:214638347-214638348	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs565538330	chr1:214638352-214638353	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs199561244	chr1:214638384-214638385	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs55849642	chr1:214638385-214638386	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs371714867	chr1:214638388-214638389	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs377677627	chr1:214638389-214638390	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs113529546	chr1:214638394-214638395	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs56248155	chr1:214638396-214638397	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs371666830	chr1:214638408-214638409	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557553342	chr1:214638418-214638419	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs5020617	chr1:214638419-214638420	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:90)

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
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	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
Basal cell lymphoma	17170743	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
Breast cancer	22522925	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:214613000-214649400	Weak transcription	Lung	lung
2	chr1:214621000-214639800	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr1:214625800-214644800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:214627200-214640000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr1:214628600-214640600	Weak transcription	Right Atrium	heart
6	chr1:214628800-214639400	Weak transcription	Stomach Mucosa	stomach
7	chr1:214629200-214644800	Weak transcription	Psoas Muscle	Psoas
8	chr1:214633600-214638000	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:214634000-214638600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr1:214634200-214638000	Weak transcription	Pancreas	Pancrea
11	chr1:214634200-214640000	Weak transcription	Fetal Kidney	kidney
12	chr1:214634400-214639800	Weak transcription	Fetal Lung	lung
13	chr1:214634400-214639800	Weak transcription	A549	lung
14	chr1:214634400-214640000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr1:214634400-214644400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr1:214634400-214645000	Weak transcription	HUVEC	blood vessel
17	chr1:214634400-214646200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr1:214634800-214638200	Strong transcription	Fetal Intestine Large	intestine
19	chr1:214634800-214640000	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr1:214635000-214638400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr1:214635000-214638600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr1:214635200-214638400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr1:214635600-214638000	Genic enhancers	HMEC	breast
24	chr1:214635800-214638200	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr1:214635800-214645000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr1:214636000-214638600	Strong transcription	NHLF	lung
27	chr1:214636200-214640600	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr1:214636400-214638200	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr1:214636400-214638600	Enhancers	Fetal Heart	heart
30	chr1:214636600-214638000	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr1:214636800-214638200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr1:214636800-214638200	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr1:214636800-214638200	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr1:214636800-214638200	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr1:214636800-214638200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr1:214636800-214638200	Strong transcription	Adipose Nuclei	Adipose
37	chr1:214636800-214638400	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr1:214636800-214638400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr1:214636800-214638400	Genic enhancers	HSMM	muscle
40	chr1:214636800-214638600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr1:214636800-214638600	Genic enhancers	NHEK	skin
42	chr1:214637000-214638000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr1:214637000-214638000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr1:214637000-214638200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr1:214637000-214638200	Genic enhancers	Muscle Satellite Cultured Cells	--
46	chr1:214637000-214638200	Strong transcription	Fetal Intestine Small	intestine
47	chr1:214637000-214638400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr1:214637000-214638800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr1:214637000-214639800	Weak transcription	NH-A	brain
50	chr1:214637000-214640200	Weak transcription	Skeletal Muscle Male	skeletal muscle

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