Variant report

Variant	nsv875755
Chromosome Location	chr2:209563753-209745017
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:473)
CpG islands
(count:183)
Chromatin interactive
region (count:16)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:473 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:209685060-209685323	K562	blood:	n/a	n/a
2	ARID3A	chr2:209659058-209659506	HepG2	liver:	n/a	n/a
3	ATF2	chr2:209737301-209737657	GM12878	blood:	n/a	n/a
4	BATF	chr2:209737343-209737641	GM12878	blood:	n/a	chr2:209737513-209737524 chr2:209737496-209737506 chr2:209737495-209737506
5	BATF	chr2:209737400-209737654	GM12878	blood:	n/a	chr2:209737513-209737524 chr2:209737496-209737506 chr2:209737495-209737506
6	BCL3	chr2:209737244-209737665	GM12878	blood:	n/a	chr2:209737495-209737504
7	BRCA1	chr2:209717948-209717972	H1-hESC	embryonic stem cell:	n/a	n/a
8	CBX3	chr2:209719485-209719729	K562	blood:	n/a	n/a
9	CEBPB	chr2:209572937-209573026	HepG2	liver:	n/a	chr2:209573004-209573015
10	CEBPB	chr2:209574657-209574903	K562	blood:	n/a	chr2:209574766-209574775 chr2:209574766-209574775 chr2:209574766-209574775 chr2:209574772-209574785 chr2:209574766-209574775 chr2:209574764-209574777 chr2:209574765-209574776 chr2:209574764-209574775 chr2:209574774-209574783
11	CEBPB	chr2:209663540-209663817	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:209647928-209648250	MCF-7	breast:	n/a	n/a
13	CEBPB	chr2:209590186-209590464	K562	blood:	n/a	n/a
14	CEBPB	chr2:209603588-209603904	A549	lung:	n/a	chr2:209603754-209603765
15	CEBPB	chr2:209695475-209695722	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:209659134-209659415	HepG2	liver:	n/a	n/a
17	CEBPB	chr2:209590990-209591321	HepG2	liver:	n/a	chr2:209591097-209591108 chr2:209591095-209591106 chr2:209591095-209591108
18	CEBPB	chr2:209674678-209674763	K562	blood:	n/a	n/a
19	CEBPB	chr2:209737278-209737281	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr2:209647865-209648259	MCF-7	breast:	n/a	n/a
21	CEBPB	chr2:209574627-209574862	HepG2	liver:	n/a	chr2:209574766-209574775 chr2:209574766-209574775 chr2:209574766-209574775 chr2:209574772-209574785 chr2:209574766-209574775 chr2:209574764-209574777 chr2:209574765-209574776 chr2:209574764-209574775 chr2:209574774-209574783
22	CEBPB	chr2:209591045-209591359	A549	lung:	n/a	chr2:209591097-209591108 chr2:209591095-209591106 chr2:209591095-209591108
23	CEBPB	chr2:209647963-209648225	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr2:209603581-209603919	HepG2	liver:	n/a	chr2:209603754-209603765
25	CEBPD	chr2:209590939-209591449	K562	blood:	n/a	n/a
26	CTCF	chr2:209647991-209648244	MCF-7	breast:	n/a	n/a
27	CTCF	chr2:209685140-209685290	GM12872	blood:	n/a	chr2:209685190-209685211
28	CTCF	chr2:209685113-209685267	Spleen_OC	spleen:	n/a	chr2:209685190-209685211
29	CTCF	chr2:209685046-209685468	SK-N-SH	brain:	n/a	chr2:209685190-209685211
30	CTCF	chr2:209685120-209685270	SK-N-SH_RA	brain:	n/a	chr2:209685190-209685211
31	CTCF	chr2:209685108-209685258	GM10248	blood:	n/a	chr2:209685190-209685211
32	CTCF	chr2:209684980-209685130	GM12865	blood:	n/a	n/a
33	CTCF	chr2:209697072-209697141	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr2:209648020-209648170	HMEC	breast:	n/a	n/a
35	CTCF	chr2:209685028-209685263	SK-N-SH_RA	brain:	n/a	chr2:209685190-209685211
36	CTCF	chr2:209648060-209648210	GM12878	blood:	n/a	n/a
37	CTCF	chr2:209648060-209648210	SAEC	small airway:	n/a	n/a
38	CTCF	chr2:209685087-209685304	LNCaP	prostate:	n/a	chr2:209685190-209685211
39	CTCF	chr2:209648040-209648190	Caco-2	colon:	n/a	n/a
40	CTCF	chr2:209645900-209646050	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:209648059-209648181	NHEK	skin:	n/a	n/a
42	CTCF	chr2:209646061-209646104	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr2:209648020-209648170	RPTEC	kidney:	n/a	n/a
44	CTCF	chr2:209685000-209685150	HepG2	liver:	n/a	n/a
45	CTCF	chr2:209648020-209648170	HRE	kidney:	n/a	n/a
46	CTCF	chr2:209685140-209685290	BE2_C	brain:	n/a	chr2:209685190-209685211
47	CTCF	chr2:209685119-209685264	Lung_OC	lung:	n/a	chr2:209685190-209685211
48	CTCF	chr2:209685140-209685290	HCT-116	colon:	n/a	chr2:209685190-209685211
49	CTCF	chr2:209685100-209685250	HCT-116	colon:	n/a	chr2:209685190-209685211
50	CTCF	chr2:209685100-209685321	LNCaP	prostate:	n/a	chr2:209685190-209685211

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:209665687-209665737	H1-hESC	embryonic stem cell:	embryo
2	chr2:209665687-209665737	HCPEpiC	choroid plexus:	n/a
3	chr2:209675250-209675300	HUVEC	blood vessel:	n/a
4	chr2:209675250-209675300	HNPCEpiC	eye:	n/a
5	chr2:209665687-209665737	PrEC	prostate:	n/a
6	chr2:209665687-209665737	SK-N-SH	brain:	n/a
7	chr2:209665525-209665575	GM06990	blood:	n/a
8	chr2:209675250-209675300	PANC-1	pancreas:	n/a
9	chr2:209665687-209665737	NHBE	bronchial:	n/a
10	chr2:209665687-209665737	GM19239	blood:	n/a
11	chr2:209665525-209665575	HCF	heart:	n/a
12	chr2:209665687-209665737	GM06990	blood:	n/a
13	chr2:209675250-209675300	HCPEpiC	choroid plexus:	n/a
14	chr2:209675250-209675300	U87	brain:	n/a
15	chr2:209665525-209665575	HMEC	breast:	n/a
16	chr2:209675250-209675300	RPTEC	kidney:	n/a
17	chr2:209665525-209665575	MCF-7	breast:	n/a
18	chr2:209665687-209665737	SK-N-MC	brain:	n/a
19	chr2:209665687-209665737	GM12878	blood:	n/a
20	chr2:209675250-209675300	ProgFib	skin:	n/a
21	chr2:209675250-209675300	HRCEpiC	kidney:	n/a
22	chr2:209665687-209665737	NT2-D1	testis:	n/a
23	chr2:209675250-209675300	ECC-1	luminal epithelium:	n/a
24	chr2:209665525-209665575	HIPEpiC	eye:	n/a
25	chr2:209675250-209675300	Caco-2	colon:	n/a
26	chr2:209665525-209665575	H1-hESC	embryonic stem cell:	embryo
27	chr2:209675250-209675300	A549	lung:	n/a
28	chr2:209665525-209665575	Hela-S3	cervix:	n/a
29	chr2:209665525-209665575	GM19239	blood:	n/a
30	chr2:209665687-209665737	ECC-1	luminal epithelium:	n/a
31	chr2:209675250-209675300	HMEC	breast:	n/a
32	chr2:209665687-209665737	SKMC	muscle:	n/a
33	chr2:209665525-209665575	HL-60	blood:	n/a
34	chr2:209665687-209665737	HL-60	blood:	n/a
35	chr2:209665687-209665737	HAEpiC	amniotic membrane:	n/a
36	chr2:209665525-209665575	BE2_C	brain:	n/a
37	chr2:209665687-209665737	LNCaP	prostate:	n/a
38	chr2:209675250-209675300	GM12892	blood:	n/a
39	chr2:209665687-209665737	NB4	blood:	n/a
40	chr2:209665687-209665737	HNPCEpiC	eye:	n/a
41	chr2:209675250-209675300	Hela-S3	cervix:	n/a
42	chr2:209665525-209665575	NH-A	brain:	n/a
43	chr2:209665687-209665737	ProgFib	skin:	n/a
44	chr2:209665687-209665737	HEEpiC	esophagus:	n/a
45	chr2:209665525-209665575	NB4	blood:	n/a
46	chr2:209665687-209665737	A549	lung:	n/a
47	chr2:209675250-209675300	PFSK-1	brain:	n/a
48	chr2:209665687-209665737	BJ	skin:	n/a
49	chr2:209665525-209665575	HCM	heart:	n/a
50	chr2:209665687-209665737	NHDF-neo	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr17:57913918..57916820-chr2:209672762..209674556,2	MCF-7	breast:
2	chr2:209331040..209332088-chr2:209646823..209648108,3	MCF-7	breast:
3	chr16:12332624..12333395-chr2:209658770..209659354,2	MCF-7	breast:
4	chr2:209685011..209685630-chr2:210072613..210073438,3	MCF-7	breast:
5	chr2:209522358..209523062-chr2:209647609..209648423,2	MCF-7	breast:
6	chr2:209572295..209574626-chr2:209585483..209587348,2	K562	blood:
7	chr2:209572295..209574626-chr2:209585483..209587348,2	K562	blood:
8	chr2:209684819..209685719-chr2:210072640..210073642,4	MCF-7	breast:
9	chr2:209566175..209569038-chr2:209578092..209580670,2	K562	blood:
10	chr2:209658091..209661078-chr2:209663650..209665764,2	K562	blood:
11	chr2:209742377..209744690-chr2:209780738..209782515,2	MCF-7	breast:
12	chr2:209735243..209737583-chr2:209791318..209793308,2	MCF-7	breast:
13	chr2:209658091..209661078-chr2:209663650..209665764,2	K562	blood:
14	chr2:209736383..209738259-chr2:210013383..210015250,2	MCF-7	breast:
15	chr2:209566175..209569038-chr2:209578092..209580670,2	K562	blood:
16	chr2:209684682..209685324-chr2:209961529..209962479,2	MCF-7	breast:

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

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

No data

Variant related genes	Relation type
PTH2R	TF binding region
PTH2R	CpG island
ENSG00000227430	chromatin interactions
ENSG00000062716	chromatin interactions

Extended variants
information (count: 1737 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1737 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1914403	chr2:209563753-209563754	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs534178336	chr2:209563754-209563755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs578154268	chr2:209563815-209563816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554188477	chr2:209563855-209563856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571873283	chr2:209563871-209563872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs545725218	chr2:209563901-209563902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570760638	chr2:209563912-209563913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs114558251	chr2:209563933-209563934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564039032	chr2:209563937-209563938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs188084127	chr2:209563954-209563955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192657608	chr2:209563969-209563970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544035143	chr2:209563988-209563989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554233106	chr2:209563993-209563994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs531249122	chr2:209564010-209564011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374029428	chr2:209564029-209564030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539953970	chr2:209564043-209564044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs560051691	chr2:209564128-209564129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs75098750	chr2:209564141-209564142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs183660892	chr2:209564167-209564168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563201071	chr2:209564223-209564224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs79085990	chr2:209564265-209564266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs78879247	chr2:209564287-209564288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs367603063	chr2:209564288-209564289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568567272	chr2:209564315-209564316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs527739485	chr2:209564369-209564370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547584905	chr2:209564384-209564385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs375200880	chr2:209564390-209564391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs142941490	chr2:209577201-209577202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185130889	chr2:209577229-209577230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs554501730	chr2:209577252-209577253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs577565570	chr2:209577285-209577286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs369220374	chr2:209577365-209577366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs76309699	chr2:209577386-209577387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs575302725	chr2:209577623-209577624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs552631373	chr2:209577635-209577636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs527670984	chr2:209577662-209577663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs142887799	chr2:209577702-209577703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs200978193	chr2:209577820-209577821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs564145527	chr2:209577862-209577863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs77916347	chr2:209577932-209577933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532237136	chr2:209577967-209577968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs1400650	chr2:209577968-209577969	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs16841683	chr2:209578018-209578019	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs531565804	chr2:209578025-209578026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183241123	chr2:209578064-209578065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs568192314	chr2:209578087-209578088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs187229102	chr2:209578116-209578117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs553762234	chr2:209578117-209578118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs528638135	chr2:209578147-209578148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570479235	chr2:209578149-209578150	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209562000-209563800	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr2:209562000-209563800	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr2:209562000-209564200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:209562200-209564000	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr2:209563600-209564400	Enhancers	Fetal Lung	lung
6	chr2:209577200-209577400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr2:209577600-209578400	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr2:209577800-209578000	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr2:209577800-209578200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr2:209577800-209578200	Enhancers	Brain Hippocampus Middle	brain
11	chr2:209577800-209578400	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr2:209578000-209578200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr2:209578000-209578200	Enhancers	Fetal Heart	heart
14	chr2:209578200-209583200	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr2:209578400-209579600	Weak transcription	Fetal Heart	heart
16	chr2:209579400-209579800	Enhancers	Duodenum Mucosa	Duodenum
17	chr2:209579600-209580200	Enhancers	Duodenum Smooth Muscle	Duodenum
18	chr2:209579600-209581000	Enhancers	Fetal Heart	heart
19	chr2:209580200-209580600	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr2:209580600-209581000	Enhancers	Duodenum Smooth Muscle	Duodenum
21	chr2:209582800-209584400	Enhancers	Fetal Intestine Small	intestine
22	chr2:209583000-209583200	Enhancers	Fetal Intestine Large	intestine
23	chr2:209583200-209584400	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr2:209583200-209587600	Weak transcription	Fetal Intestine Large	intestine
25	chr2:209583400-209584400	Enhancers	Rectal Mucosa Donor 29	rectum
26	chr2:209584400-209587200	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr2:209584400-209587400	Weak transcription	Fetal Intestine Small	intestine
28	chr2:209587200-209588000	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr2:209587400-209588400	Enhancers	Fetal Intestine Small	intestine
30	chr2:209587600-209588400	Enhancers	Fetal Intestine Large	intestine
31	chr2:209587800-209588400	Enhancers	Small Intestine	intestine
32	chr2:209596000-209596200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr2:209596000-209596400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr2:209596000-209596400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr2:209621600-209622800	Enhancers	Fetal Heart	heart
36	chr2:209645800-209646400	Enhancers	Fetal Heart	heart
37	chr2:209645800-209646800	Enhancers	Colon Smooth Muscle	Colon
38	chr2:209646400-209647400	Weak transcription	Fetal Heart	heart
39	chr2:209647800-209648000	Enhancers	Fetal Heart	heart
40	chr2:209649000-209649800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
41	chr2:209658400-209659400	Enhancers	HepG2	liver
42	chr2:209658600-209659000	Enhancers	Liver	Liver
43	chr2:209658600-209659400	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr2:209659000-209659400	Flanking Active TSS	Liver	Liver
45	chr2:209659400-209659600	Enhancers	Liver	Liver
46	chr2:209663000-209664000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr2:209663200-209664000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr2:209663400-209664000	Enhancers	H9 Cell Line	embryonic stem cell
49	chr2:209665200-209665800	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr2:209672000-209673000	Active TSS	A549	lung

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