Variant report

Variant	esv3487576
Chromosome Location	chr2:209768379-209947296
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:458)
CpG islands
(count:123)
Chromatin interactive
region (count:21)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:458 , 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	chr2:209794158-209795186	K562	blood:	n/a	n/a
2	ARID3A	chr2:209850333-209850752	K562	blood:	n/a	n/a
3	ATF1	chr2:209794131-209794489	K562	blood:	n/a	n/a
4	ATF1	chr2:209906096-209906295	K562	blood:	n/a	n/a
5	ATF1	chr2:209850478-209850694	K562	blood:	n/a	n/a
6	ATF3	chr2:209794080-209794482	K562	blood:	n/a	n/a
7	BACH1	chr2:209875885-209876024	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr2:209906062-209906412	K562	blood:	n/a	n/a
9	BHLHE40	chr2:209794062-209794557	K562	blood:	n/a	n/a
10	CBX3	chr2:209794120-209794443	K562	blood:	n/a	n/a
11	CCNT2	chr2:209784118-209784314	K562	blood:	n/a	n/a
12	CCNT2	chr2:209794180-209794575	K562	blood:	n/a	n/a
13	CEBPB	chr2:209840198-209840398	HepG2	liver:	n/a	chr2:209840308-209840319
14	CEBPB	chr2:209851799-209851995	HepG2	liver:	n/a	chr2:209851907-209851918
15	CEBPB	chr2:209864598-209865094	MCF-7	breast:	n/a	chr2:209864704-209864715 chr2:209864704-209864715
16	CEBPB	chr2:209780898-209781061	HepG2	liver:	n/a	n/a
17	CEBPB	chr2:209794140-209794400	K562	blood:	n/a	n/a
18	CEBPB	chr2:209780201-209780442	HepG2	liver:	n/a	chr2:209780302-209780313
19	CEBPB	chr2:209864574-209864995	MCF-7	breast:	n/a	chr2:209864704-209864715 chr2:209864704-209864715
20	CEBPB	chr2:209819295-209819471	A549	lung:	n/a	n/a
21	CEBPB	chr2:209794118-209794467	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr2:209794090-209794533	HCT-116	colon:	n/a	n/a
23	CEBPB	chr2:209780940-209781055	A549	lung:	n/a	n/a
24	CEBPB	chr2:209925339-209925581	HepG2	liver:	n/a	chr2:209925520-209925531 chr2:209925518-209925529
25	CEBPB	chr2:209801456-209801658	HepG2	liver:	n/a	chr2:209801535-209801546 chr2:209801535-209801548 chr2:209801535-209801548
26	CEBPB	chr2:209793962-209794584	HCT-116	colon:	n/a	n/a
27	CEBPB	chr2:209794078-209794516	MCF-7	breast:	n/a	n/a
28	CEBPB	chr2:209935544-209935609	HepG2	liver:	n/a	chr2:209935580-209935591
29	CEBPB	chr2:209848245-209848598	MCF-7	breast:	n/a	n/a
30	CEBPB	chr2:209875950-209876151	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr2:209794129-209794505	K562	blood:	n/a	n/a
32	CEBPB	chr2:209794128-209794619	MCF-7	breast:	n/a	n/a
33	CEBPB	chr2:209925435-209925658	A549	lung:	n/a	chr2:209925520-209925531 chr2:209925518-209925529
34	CEBPB	chr2:209794077-209794522	K562	blood:	n/a	n/a
35	CEBPB	chr2:209848087-209848667	MCF-7	breast:	n/a	n/a
36	CEBPB	chr2:209883491-209883673	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPD	chr2:209794118-209794484	K562	blood:	n/a	n/a
38	CEBPD	chr2:209850457-209850711	K562	blood:	n/a	n/a
39	CTCF	chr2:209895620-209895770	GM12872	blood:	n/a	n/a
40	CTCF	chr2:209914500-209914650	HMEC	breast:	n/a	n/a
41	CTCF	chr2:209873768-209873825	HepG2	liver:	n/a	n/a
42	CTCF	chr2:209870799-209870845	GM13976	blood:	n/a	n/a
43	CTCF	chr2:209771719-209771760	GM19238	blood:	n/a	n/a
44	CTCF	chr2:209902720-209902870	MCF-7	breast:	n/a	n/a
45	CTCF	chr2:209914480-209914630	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr2:209870849-209870852	GM13976	blood:	n/a	n/a
47	CTCF	chr2:209771762-209771763	HepG2	liver:	n/a	n/a
48	CTCF	chr2:209830240-209830390	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr2:209895600-209895750	GM12878	blood:	n/a	n/a
50	CTCF	chr2:209771695-209771751	GM19240	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:209854267-209854317	MCF-7	breast:	n/a
2	chr2:209854267-209854317	MCF-7	breast:	n/a
3	chr2:209874962-209875012	Hepatocyte	liver:	n/a
4	chr2:209874962-209875012	LNCaP	prostate:	n/a
5	chr2:209874962-209875012	ovcar-3	ovarian:	n/a
6	chr2:209854267-209854317	SK-N-SH	brain:	n/a
7	chr2:209874962-209875012	HepG2	liver:	n/a
8	chr2:209874962-209875012	HL-60	blood:	n/a
9	chr2:209854267-209854317	PANC-1	pancreas:	n/a
10	chr2:209854267-209854317	HCPEpiC	choroid plexus:	n/a
11	chr2:209874962-209875012	BJ	skin:	n/a
12	chr2:209854267-209854317	PFSK-1	brain:	n/a
13	chr2:209874962-209875012	HCM	heart:	n/a
14	chr2:209874962-209875012	ECC-1	luminal epithelium:	n/a
15	chr2:209854267-209854317	HEEpiC	esophagus:	n/a
16	chr2:209854267-209854317	AoSMC	blood vessel:	n/a
17	chr2:209854267-209854317	GM12878	blood:	n/a
18	chr2:209874962-209875012	HEK293	kidney:	embryo
19	chr2:209854267-209854317	IMR90	lung:	fetal
20	chr2:209874962-209875012	MCF10A-Er-Src	breast:	n/a
21	chr2:209854267-209854317	SK-N-MC	brain:	n/a
22	chr2:209874962-209875012	GM06990	blood:	n/a
23	chr2:209854267-209854317	SKMC	muscle:	n/a
24	chr2:209874962-209875012	T-47D	breast:	n/a
25	chr2:209854267-209854317	NT2-D1	testis:	n/a
26	chr2:209854267-209854317	HNPCEpiC	eye:	n/a
27	chr2:209874962-209875012	HCT-116	colon:	n/a
28	chr2:209874962-209875012	HRCEpiC	kidney:	n/a
29	chr2:209874962-209875012	NHBE	bronchial:	n/a
30	chr2:209854267-209854317	SK-N-SH_RA	brain:	n/a
31	chr2:209874962-209875012	AG09309	skin:	n/a
32	chr2:209854267-209854317	MCF10A-Er-Src	breast:	n/a
33	chr2:209874962-209875012	HUVEC	blood vessel:	n/a
34	chr2:209854267-209854317	HMEC	breast:	n/a
35	chr2:209854267-209854317	T-47D	breast:	n/a
36	chr2:209874962-209875012	AG04450	lung:	fetal
37	chr2:209854267-209854317	ProgFib	skin:	n/a
38	chr2:209854267-209854317	Hela-S3	cervix:	n/a
39	chr2:209854267-209854317	AG04450	lung:	fetal
40	chr2:209874962-209875012	HAEpiC	amniotic membrane:	n/a
41	chr2:209874962-209875012	HIPEpiC	eye:	n/a
42	chr2:209874962-209875012	HRPEpiC	eye:	n/a
43	chr2:209854267-209854317	AG04449	skin:	fetal
44	chr2:209874962-209875012	IMR90	lung:	fetal
45	chr2:209874962-209875012	SK-N-SH_RA	brain:	n/a
46	chr2:209874962-209875012	HCPEpiC	choroid plexus:	n/a
47	chr2:209854267-209854317	HCT-116	colon:	n/a
48	chr2:209874962-209875012	NT2-D1	testis:	n/a
49	chr2:209854267-209854317	NHBE	bronchial:	n/a
50	chr2:209874962-209875012	MCF-7	breast:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:209812335..209815569-chr2:209817541..209819939,3	K562	blood:
2	chr2:209923719..209926042-chr2:209927287..209929588,2	K562	blood:
3	chr2:209812335..209815569-chr2:209817541..209819939,3	K562	blood:
4	chr2:209788994..209791751-chr2:209794523..209798556,3	K562	blood:
5	chr2:209742377..209744690-chr2:209780738..209782515,2	MCF-7	breast:
6	chr2:209781804..209784623-chr2:209788415..209790919,2	K562	blood:
7	chr2:209878244..209880957-chr2:209882078..209884649,2	MCF-7	breast:
8	chr2:209781804..209784623-chr2:209788415..209790919,2	K562	blood:
9	chr2:209801606..209803853-chr2:209820902..209823533,2	MCF-7	breast:
10	chr2:209735243..209737583-chr2:209791318..209793308,2	MCF-7	breast:
11	chr2:209852263..209854117-chr2:209855293..209858192,2	K562	blood:
12	chr2:209852263..209854117-chr2:209855293..209858192,2	K562	blood:
13	chr2:209788994..209791751-chr2:209794523..209798556,3	K562	blood:
14	chr2:209801606..209803853-chr2:209820902..209823533,2	MCF-7	breast:
15	chr2:209911421..209913579-chr2:209913671..209915928,2	MCF-7	breast:
16	chr2:209795500..209797235-chr2:209799096..209800805,2	K562	blood:
17	chr2:209795500..209797235-chr2:209799096..209800805,2	K562	blood:
18	chr2:209911421..209913579-chr2:209913671..209915928,2	MCF-7	breast:
19	chr2:209923719..209926042-chr2:209927287..209929588,2	K562	blood:
20	chr2:209878244..209880957-chr2:209882078..209884649,2	MCF-7	breast:
21	chr14:35871895..35874514-chr2:209813053..209815849,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTH2R-2	chr2:209894597-209894764	l_2022_chr2:209894596-209898538_76bGuttman_hES
2	lnc-PTH2R-2	chr2:209896369-209898538	l_2022_chr2:209894596-209898538_76bGuttman_hES
3	lnc-IDH1-4	chr2:209907730-209907770	NONHSAT076653
4	lnc-IDH1-4	chr2:209914528-209914662	NONHSAT076653

No data

Variant related genes	Relation type
HSPA8P6	TF binding region
RNA5SP117	TF binding region
HSPA8P6	CpG island
RNA5SP117	CpG island
ENSG00000100906	chromatin interactions

Extended variants
information (count: 2678 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2678 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182950249	chr2:209768430-209768431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs560929806	chr2:209768433-209768434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529897617	chr2:209768478-209768479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187667788	chr2:209768505-209768506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs11681253	chr2:209768519-209768520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370079862	chr2:209768520-209768521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs13399500	chr2:209768541-209768542	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs201580565	chr2:209768542-209768543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373833958	chr2:209768555-209768556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs538544982	chr2:209768558-209768559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191374292	chr2:209768560-209768561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554348186	chr2:209768595-209768596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs73064322	chr2:209768611-209768612	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs534393929	chr2:209768629-209768630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182806480	chr2:209768658-209768659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188274437	chr2:209768698-209768699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs539519760	chr2:209768706-209768707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556148200	chr2:209768743-209768744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575982047	chr2:209768775-209768776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544145990	chr2:209768838-209768839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561225199	chr2:209768839-209768840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574578131	chr2:209768843-209768844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540397445	chr2:209768848-209768849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574107634	chr2:209768849-209768850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192210216	chr2:209768861-209768862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552264611	chr2:209768880-209768881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562473409	chr2:209768942-209768943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531331274	chr2:209768952-209768953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs548643354	chr2:209768961-209768962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372306334	chr2:209769012-209769013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568722481	chr2:209769022-209769023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs74662213	chr2:209769063-209769064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs78117369	chr2:209769075-209769076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183664936	chr2:209769078-209769079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs13427915	chr2:209769080-209769081	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs76619362	chr2:209769084-209769085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs76548362	chr2:209769097-209769098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs4485688	chr2:209769098-209769099	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs539549365	chr2:209769099-209769100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34988180	chr2:209769100-209769101	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs75283024	chr2:209769140-209769141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs79783357	chr2:209769157-209769158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs76663155	chr2:209769162-209769163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576067186	chr2:209769167-209769168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs80228738	chr2:209769169-209769170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs75670269	chr2:209769177-209769178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs75767941	chr2:209769189-209769190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78380827	chr2:209769192-209769193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs79176969	chr2:209769201-209769202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs74729991	chr2:209769214-209769215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209767600-209770200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr2:209770000-209770800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr2:209770000-209772000	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr2:209770000-209772200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr2:209770200-209772200	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr2:209770800-209771000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
7	chr2:209770800-209771600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr2:209770800-209771600	Enhancers	H9 Cell Line	embryonic stem cell
9	chr2:209770800-209772400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr2:209771000-209771200	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr2:209771000-209771600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr2:209771000-209772000	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr2:209771200-209771400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
14	chr2:209771200-209772200	Enhancers	H1 Cell Line	embryonic stem cell
15	chr2:209771400-209772000	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr2:209772200-209772600	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr2:209772200-209773200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr2:209772400-209772800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr2:209772600-209773000	Enhancers	H1 Cell Line	embryonic stem cell
20	chr2:209772800-209773400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr2:209773200-209773400	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr2:209778400-209779000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr2:209778600-209779000	Enhancers	H9 Cell Line	embryonic stem cell
24	chr2:209792400-209793600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr2:209793200-209793600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr2:209794000-209795200	Enhancers	K562	blood
27	chr2:209796600-209810800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr2:209804600-209805200	Enhancers	Placenta Amnion	Placenta Amnion
29	chr2:209809200-209809400	Enhancers	Colon Smooth Muscle	Colon
30	chr2:209810800-209811200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr2:209810800-209811200	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr2:209810800-209811200	Enhancers	NHEK	skin
33	chr2:209811000-209811600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr2:209811600-209818400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr2:209815000-209816000	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr2:209842800-209843000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr2:209843000-209853600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr2:209843800-209844200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr2:209843800-209844200	Enhancers	NHEK	skin
40	chr2:209844200-209847000	Weak transcription	NHEK	skin
41	chr2:209844200-209848600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr2:209847000-209850000	Enhancers	NHEK	skin
43	chr2:209847200-209848000	Enhancers	Placenta Amnion	Placenta Amnion
44	chr2:209847200-209848000	Enhancers	HMEC	breast
45	chr2:209847200-209849800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr2:209847800-209848000	Enhancers	Placenta	Placenta
47	chr2:209847800-209849800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr2:209848000-209849000	Weak transcription	Placenta	Placenta
49	chr2:209848000-209849000	Weak transcription	HMEC	breast
50	chr2:209848000-209851000	Weak transcription	Placenta Amnion	Placenta Amnion

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