Variant report

Variant	nsv460057
Chromosome Location	chr2:209659222-209736009
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:231)
CpG islands
(count:184)
Chromatin interactive
region (count:8)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:231 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:209659058-209659506	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:209685060-209685323	K562	blood:	n/a	n/a
3	BRCA1	chr2:209717948-209717972	H1-hESC	embryonic stem cell:	n/a	n/a
4	CBX3	chr2:209719485-209719729	K562	blood:	n/a	n/a
5	CEBPB	chr2:209659134-209659415	HepG2	liver:	n/a	n/a
6	CEBPB	chr2:209695475-209695722	HepG2	liver:	n/a	n/a
7	CEBPB	chr2:209674678-209674763	K562	blood:	n/a	n/a
8	CEBPB	chr2:209663540-209663817	HepG2	liver:	n/a	n/a
9	CTCF	chr2:209684580-209684730	HRE	kidney:	n/a	n/a
10	CTCF	chr2:209685120-209685270	K562	blood:	n/a	chr2:209685190-209685211
11	CTCF	chr2:209685180-209685330	SAEC	small airway:	n/a	chr2:209685190-209685211
12	CTCF	chr2:209685113-209685267	Spleen_OC	spleen:	n/a	chr2:209685190-209685211
13	CTCF	chr2:209685093-209685291	MCF-7	breast:	n/a	chr2:209685190-209685211
14	CTCF	chr2:209685120-209685270	GM12870	blood:	n/a	chr2:209685190-209685211
15	CTCF	chr2:209685092-209685307	A549	lung:	n/a	chr2:209685190-209685211
16	CTCF	chr2:209685140-209685290	HCT-116	colon:	n/a	chr2:209685190-209685211
17	CTCF	chr2:209725340-209725490	GM12867	blood:	n/a	n/a
18	CTCF	chr2:209685120-209685270	GM12878	blood:	n/a	chr2:209685190-209685211
19	CTCF	chr2:209685080-209685230	SK-N-SH_RA	brain:	n/a	chr2:209685190-209685211
20	CTCF	chr2:209685129-209685293	GM12878	blood:	n/a	chr2:209685190-209685211
21	CTCF	chr2:209685140-209685290	HMEC	breast:	n/a	chr2:209685190-209685211
22	CTCF	chr2:209714789-209714791	LNCaP	prostate:	n/a	n/a
23	CTCF	chr2:209685000-209685150	HepG2	liver:	n/a	n/a
24	CTCF	chr2:209685140-209685290	GM12872	blood:	n/a	chr2:209685190-209685211
25	CTCF	chr2:209685140-209685290	BE2_C	brain:	n/a	chr2:209685190-209685211
26	CTCF	chr2:209685100-209685250	Caco-2	colon:	n/a	chr2:209685190-209685211
27	CTCF	chr2:209685140-209685290	GM12874	blood:	n/a	chr2:209685190-209685211
28	CTCF	chr2:209685100-209685250	WERI-Rb-1	eye:	n/a	chr2:209685190-209685211
29	CTCF	chr2:209685080-209685230	BE2_C	brain:	n/a	chr2:209685190-209685211
30	CTCF	chr2:209685205-209685228	Gliobla	brain:	n/a	n/a
31	CTCF	chr2:209685141-209685264	MCF-7	breast:	n/a	chr2:209685190-209685211
32	CTCF	chr2:209685220-209685370	HL-60	blood:	n/a	n/a
33	CTCF	chr2:209705690-209705789	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr2:209685120-209685270	HMF	breast:	n/a	chr2:209685190-209685211
35	CTCF	chr2:209685140-209685290	HEEpiC	esophagus:	n/a	chr2:209685190-209685211
36	CTCF	chr2:209685160-209685310	GM12875	blood:	n/a	chr2:209685190-209685211
37	CTCF	chr2:209697072-209697141	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr2:209728614-209728708	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr2:209676456-209676536	MCF-7	breast:	n/a	n/a
40	CTCF	chr2:209685160-209685310	HEK293	kidney:	n/a	chr2:209685190-209685211
41	CTCF	chr2:209684954-209685388	HepG2	liver:	n/a	chr2:209685190-209685211
42	CTCF	chr2:209685120-209685270	HRPEpiC	eye:	n/a	chr2:209685190-209685211
43	CTCF	chr2:209685003-209685389	GM12878	blood:	n/a	chr2:209685190-209685211
44	CTCF	chr2:209685140-209685290	NHEK	skin:	n/a	chr2:209685190-209685211
45	CTCF	chr2:209685160-209685310	GM06990	blood:	n/a	chr2:209685190-209685211
46	CTCF	chr2:209685082-209685322	Medullo	brain:	n/a	chr2:209685190-209685211
47	CTCF	chr2:209685220-209685370	MCF-7	breast:	n/a	n/a
48	CTCF	chr2:209714735-209714783	LNCaP	prostate:	n/a	n/a
49	CTCF	chr2:209685120-209685270	MCF-7	breast:	n/a	chr2:209685190-209685211
50	CTCF	chr2:209685160-209685249	HepG2	liver:	n/a	chr2:209685190-209685211

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:209665525-209665575	NB4	blood:	n/a
2	chr2:209665525-209665575	NB4	blood:	n/a
3	chr2:209665525-209665575	MCF10A-Er-Src	breast:	n/a
4	chr2:209665687-209665737	U87	brain:	n/a
5	chr2:209675250-209675300	HepG2	liver:	n/a
6	chr2:209665525-209665575	HNPCEpiC	eye:	n/a
7	chr2:209665525-209665575	K562	blood:	n/a
8	chr2:209665687-209665737	Jurkat	blood:	n/a
9	chr2:209665525-209665575	HPAEpiC	pulmonary alveolar:	n/a
10	chr2:209665687-209665737	PrEC	prostate:	n/a
11	chr2:209665525-209665575	AG09309	skin:	n/a
12	chr2:209675250-209675300	SAEC	small airway:	n/a
13	chr2:209675250-209675300	SK-N-MC	brain:	n/a
14	chr2:209665525-209665575	HL-60	blood:	n/a
15	chr2:209675250-209675300	HCF	heart:	n/a
16	chr2:209675250-209675300	IMR90	lung:	fetal
17	chr2:209665525-209665575	LNCaP	prostate:	n/a
18	chr2:209675250-209675300	PFSK-1	brain:	n/a
19	chr2:209675250-209675300	Hela-S3	cervix:	n/a
20	chr2:209665525-209665575	Jurkat	blood:	n/a
21	chr2:209665687-209665737	SK-N-SH	brain:	n/a
22	chr2:209675250-209675300	ECC-1	luminal epithelium:	n/a
23	chr2:209665687-209665737	CMK	blood:	n/a
24	chr2:209675250-209675300	HEK293	kidney:	embryo
25	chr2:209665525-209665575	NHBE	bronchial:	n/a
26	chr2:209665687-209665737	HL-60	blood:	n/a
27	chr2:209665687-209665737	K562	blood:	n/a
28	chr2:209665525-209665575	HAEpiC	amniotic membrane:	n/a
29	chr2:209665687-209665737	HEK293	kidney:	embryo
30	chr2:209665687-209665737	AG04450	lung:	fetal
31	chr2:209665687-209665737	Hepatocyte	liver:	n/a
32	chr2:209665687-209665737	IMR90	lung:	fetal
33	chr2:209675250-209675300	Caco-2	colon:	n/a
34	chr2:209665525-209665575	GM12892	blood:	n/a
35	chr2:209675250-209675300	HRPEpiC	eye:	n/a
36	chr2:209675250-209675300	ProgFib	skin:	n/a
37	chr2:209665687-209665737	GM12891	blood:	n/a
38	chr2:209665525-209665575	CMK	blood:	n/a
39	chr2:209675250-209675300	AG04450	lung:	fetal
40	chr2:209665687-209665737	SAEC	small airway:	n/a
41	chr2:209665525-209665575	SK-N-SH_RA	brain:	n/a
42	chr2:209675250-209675300	HCM	heart:	n/a
43	chr2:209665687-209665737	Caco-2	colon:	n/a
44	chr2:209665687-209665737	SK-N-SH_RA	brain:	n/a
45	chr2:209665525-209665575	HIPEpiC	eye:	n/a
46	chr2:209675250-209675300	NB4	blood:	n/a
47	chr2:209665525-209665575	HCPEpiC	choroid plexus:	n/a
48	chr2:209665525-209665575	NH-A	brain:	n/a
49	chr2:209675250-209675300	HAEpiC	amniotic membrane:	n/a
50	chr2:209665687-209665737	LNCaP	prostate:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:209658091..209661078-chr2:209663650..209665764,2	K562	blood:
2	chr2:209684682..209685324-chr2:209961529..209962479,2	MCF-7	breast:
3	chr17:57913918..57916820-chr2:209672762..209674556,2	MCF-7	breast:
4	chr2:209658091..209661078-chr2:209663650..209665764,2	K562	blood:
5	chr16:12332624..12333395-chr2:209658770..209659354,2	MCF-7	breast:
6	chr2:209685011..209685630-chr2:210072613..210073438,3	MCF-7	breast:
7	chr2:209684819..209685719-chr2:210072640..210073642,4	MCF-7	breast:
8	chr2:209735243..209737583-chr2:209791318..209793308,2	MCF-7	breast:

(count:28 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTH2R-1	chr2:209709858-209709950	NONHSAT076649
2	lnc-PTH2R-1	chr2:209688919-209689074	NONHSAT076646
3	lnc-PTH2R-1	chr2:209719024-209719090	NONHSAT147141
4	lnc-PTH2R-1	chr2:209719024-209723402	NONHSAT076648
5	lnc-PTH2R-1	chr2:209704710-209704818	NONHSAT076651
6	lnc-PTH2R-1	chr2:209688919-209689074	NONHSAT076648
7	lnc-PTH2R-1	chr2:209709858-209709950	NONHSAT076651
8	lnc-PTH2R-1	chr2:209719024-209720220	NONHSAT076646
9	lnc-PTH2R-1	chr2:209703087-209703135	NONHSAT076651
10	lnc-PTH2R-1	chr2:209719024-209720220	NONHSAT076645
11	lnc-PTH2R-1	chr2:209709855-209709950	NONHSAT076645
12	lnc-PTH2R-1	chr2:209709858-209709950	NONHSAT147141
13	lnc-PTH2R-1	chr2:209690123-209690431	NONHSAT076650
14	lnc-PTH2R-1	chr2:209688919-209689074	NONHSAT076649
15	lnc-PTH2R-1	chr2:209709858-209709950	NONHSAT076646
16	lnc-PTH2R-1	chr2:209687215-209687279	NONHSAT076649
17	lnc-PTH2R-1	chr2:209719024-209719227	NONHSAT076651
18	lnc-PTH2R-1	chr2:209674170-209674289	NONHSAT076649
19	lnc-PTH2R-1	chr2:209709858-209709950	NONHSAT076648
20	lnc-PTH2R-1	chr2:209688919-209689074	NONHSAT076645
21	lnc-PTH2R-1	chr2:209719024-209723402	NONHSAT076649
22	lnc-PTH2R-1	chr2:209688900-209689074	NONHSAT076650
23	lnc-PTH2R-1	chr2:209706409-209706507	NONHSAT147141
24	lnc-PTH2R-1	chr2:209674176-209674279	NONHSAT076647
25	lnc-PTH2R-1	chr2:209709858-209709950	NONHSAT076650
26	lnc-PTH2R-1	chr2:209690123-209690431	NONHSAT076648
27	lnc-PTH2R-1	chr2:209719024-209723402	NONHSAT076650
28	lnc-PTH2R-1	chr2:209706405-209706507	NONHSAT076651

No data

Variant related genes	Relation type
PTH2R	TF binding region
PTH2R	CpG island
ENSG00000062716	chromatin interactions

Extended variants
information (count: 935 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:935 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6732651	chr2:209659222-209659223	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs115071492	chr2:209659285-209659286	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185684190	chr2:209659290-209659291	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs190693156	chr2:209659292-209659293	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs181569652	chr2:209659301-209659302	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs186986645	chr2:209659309-209659310	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs527486239	chr2:209659408-209659409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs555579844	chr2:209659419-209659420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565804454	chr2:209659438-209659439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189410009	chr2:209659456-209659457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs76918738	chr2:209659471-209659472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181410410	chr2:209659493-209659494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs185311051	chr2:209659520-209659521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189972350	chr2:209659527-209659528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs145606873	chr2:209659591-209659592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs147680894	chr2:209663021-209663022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs140941266	chr2:209663040-209663041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs73056382	chr2:209663049-209663050	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs191930017	chr2:209663057-209663058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs144786838	chr2:209663101-209663102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs564285541	chr2:209663165-209663166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs539869801	chr2:209663178-209663179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556128145	chr2:209663190-209663191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs575183268	chr2:209663200-209663201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537699633	chr2:209663254-209663255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs4672537	chr2:209663256-209663257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs574538634	chr2:209663258-209663259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540035214	chr2:209663275-209663276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs145882108	chr2:209663324-209663325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs576859249	chr2:209663339-209663340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs149001423	chr2:209663389-209663390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs73056383	chr2:209663409-209663410	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs532067399	chr2:209663426-209663427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs369894306	chr2:209663470-209663471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143470412	chr2:209663471-209663472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs562230619	chr2:209663503-209663504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs150928627	chr2:209663576-209663577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs140755856	chr2:209663590-209663591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs570966630	chr2:209663597-209663598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs144697134	chr2:209663648-209663649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs1517350	chr2:209663702-209663703	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs569685311	chr2:209663718-209663719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs7566778	chr2:209663735-209663736	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs73056384	chr2:209663748-209663749	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs186654508	chr2:209663806-209663807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs6715939	chr2:209663832-209663833	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs553648429	chr2:209663837-209663838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs570534729	chr2:209663847-209663848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550039927	chr2:209663855-209663856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs371106424	chr2:209663856-209663857	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	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
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Renal cell carcinoma	18765545	CNVD
Ovarian cancer	19193619	CNVD
Non-small cell lung cancer	18676828	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Urothelial cell carcinoma	18451213	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bipolar disorder	19114987	CNVD
Developmental delay	21147756	CNVD

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209658400-209659400	Enhancers	HepG2	liver
2	chr2:209658600-209659400	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr2:209659000-209659400	Flanking Active TSS	Liver	Liver
4	chr2:209659400-209659600	Enhancers	Liver	Liver
5	chr2:209663000-209664000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:209663200-209664000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:209663400-209664000	Enhancers	H9 Cell Line	embryonic stem cell
8	chr2:209665200-209665800	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr2:209672000-209673000	Active TSS	A549	lung
10	chr2:209672400-209672800	Enhancers	HMEC	breast
11	chr2:209674200-209674800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr2:209674200-209675600	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr2:209674600-209675000	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr2:209676200-209676600	Active TSS	A549	lung
15	chr2:209684600-209685200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr2:209684600-209685400	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr2:209684600-209685400	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr2:209684600-209685600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr2:209684600-209686200	Enhancers	Fetal Heart	heart
20	chr2:209684800-209685200	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr2:209684800-209685400	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr2:209684800-209685600	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr2:209685000-209685400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr2:209685000-209685400	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr2:209685000-209685600	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr2:209691600-209692400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr2:209691800-209692800	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr2:209692000-209692800	Enhancers	Fetal Heart	heart
29	chr2:209692000-209692800	Enhancers	Pancreas	Pancrea
30	chr2:209692000-209692800	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr2:209692000-209693000	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr2:209692400-209692800	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr2:209692800-209693800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr2:209692800-209694000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr2:209692800-209694400	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr2:209693800-209694400	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr2:209694200-209695600	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr2:209694400-209695400	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr2:209710600-209713400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr2:209712400-209713400	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr2:209718200-209718600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr2:209719200-209720000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
43	chr2:209721000-209721600	Enhancers	Colon Smooth Muscle	Colon
44	chr2:209725000-209727800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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