Variant report

Variant	esv1821662
Chromosome Location	chr2:76808454-76862898
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:323)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:323 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:76826892-76827267	HepG2	liver:	n/a	n/a
2	BACH1	chr2:76826863-76827150	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr2:76826886-76827145	GM12878	blood:	n/a	n/a
4	BHLHE40	chr2:76826921-76827181	K562	blood:	n/a	n/a
5	BHLHE40	chr2:76826935-76827215	GM12878	blood:	n/a	n/a
6	BRCA1	chr2:76826858-76827249	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr2:76826891-76827167	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD1	chr2:76808522-76808533	GM12878	blood:	n/a	n/a
9	CHD2	chr2:76826886-76827202	H1-hESC	embryonic stem cell:	n/a	n/a
10	CREB1	chr2:76856448-76856731	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr2:76826810-76827289	K562	blood:	n/a	n/a
12	CTCF	chr2:76826980-76827130	GM12864	blood:	n/a	n/a
13	CTCF	chr2:76826960-76827110	GM12864	blood:	n/a	n/a
14	CTCF	chr2:76827000-76827150	NHLF	lung:	n/a	n/a
15	CTCF	chr2:76826980-76827130	GM12872	blood:	n/a	n/a
16	CTCF	chr2:76826960-76827110	NHEK	skin:	n/a	n/a
17	CTCF	chr2:76827000-76827150	HEEpiC	esophagus:	n/a	n/a
18	CTCF	chr2:76826907-76827230	Pancreas_OC	pancreas:	n/a	n/a
19	CTCF	chr2:76826920-76827070	RPTEC	kidney:	n/a	n/a
20	CTCF	chr2:76826895-76827197	K562	blood:	n/a	n/a
21	CTCF	chr2:76826980-76827130	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr2:76826980-76827130	HPAF	blood vessel:	n/a	n/a
23	CTCF	chr2:76826806-76827245	T-47D	breast:	n/a	n/a
24	CTCF	chr2:76826922-76827161	A549	lung:	n/a	n/a
25	CTCF	chr2:76826885-76827162	ECC-1	luminal epithelium:	n/a	n/a
26	CTCF	chr2:76851532-76851796	GM12878	blood:	n/a	n/a
27	CTCF	chr2:76827400-76827550	GM12868	blood:	n/a	n/a
28	CTCF	chr2:76826920-76827070	HFF	foreskin:	n/a	n/a
29	CTCF	chr2:76826804-76827231	K562	blood:	n/a	n/a
30	CTCF	chr2:76826960-76827110	SAEC	small airway:	n/a	n/a
31	CTCF	chr2:76827320-76827470	GM12878	blood:	n/a	n/a
32	CTCF	chr2:76826818-76827279	HepG2	liver:	n/a	n/a
33	CTCF	chr2:76827376-76827446	GM10266	blood:	n/a	n/a
34	CTCF	chr2:76826917-76827207	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr2:76822187-76822219	GM20000	blood:	n/a	n/a
36	CTCF	chr2:76826862-76827217	Gliobla	brain:	n/a	n/a
37	CTCF	chr2:76826946-76827150	ProgFib	skin:	n/a	n/a
38	CTCF	chr2:76826760-76826910	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr2:76826940-76827090	GM12874	blood:	n/a	n/a
40	CTCF	chr2:76826940-76827090	HCFaa	heart:	n/a	n/a
41	CTCF	chr2:76826934-76827210	GM10266	blood:	n/a	n/a
42	CTCF	chr2:76826860-76827010	HFF-Myc	foreskin:	n/a	n/a
43	CTCF	chr2:76827040-76827190	AG09309	skin:	n/a	n/a
44	CTCF	chr2:76827344-76827472	GM13977	blood:	n/a	n/a
45	CTCF	chr2:76827060-76827210	HCT-116	colon:	n/a	n/a
46	CTCF	chr2:76826877-76827167	ECC-1	luminal epithelium:	n/a	n/a
47	CTCF	chr2:76826910-76827146	MCF-7	breast:	n/a	n/a
48	CTCF	chr2:76826927-76827189	GM20000	blood:	n/a	n/a
49	CTCF	chr2:76827000-76827150	BJ	skin:	n/a	n/a
50	CTCF	chr2:76826980-76827130	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:76839078-76839128	AG09319	gingival:	n/a
2	chr2:76839078-76839128	IMR90	lung:	fetal
3	chr2:76839078-76839128	BJ	skin:	n/a
4	chr2:76839078-76839128	A549	lung:	n/a
5	chr2:76839078-76839128	SKMC	muscle:	n/a
6	chr2:76839078-76839128	HAEpiC	amniotic membrane:	n/a
7	chr2:76839078-76839128	HRCEpiC	kidney:	n/a
8	chr2:76839078-76839128	AG09309	skin:	n/a
9	chr2:76839078-76839128	Hepatocyte	liver:	n/a
10	chr2:76839078-76839128	NT2-D1	testis:	n/a
11	chr2:76839078-76839128	GM19239	blood:	n/a
12	chr2:76839078-76839128	CMK	blood:	n/a
13	chr2:76839078-76839128	PrEC	prostate:	n/a
14	chr2:76839078-76839128	GM12891	blood:	n/a
15	chr2:76839078-76839128	HRPEpiC	eye:	n/a
16	chr2:76839078-76839128	Caco-2	colon:	n/a
17	chr2:76839078-76839128	SK-N-SH	brain:	n/a
18	chr2:76839078-76839128	HRE	kidney:	n/a
19	chr2:76839078-76839128	RPTEC	kidney:	n/a
20	chr2:76839078-76839128	H1-hESC	embryonic stem cell:	embryo
21	chr2:76839078-76839128	GM12878	blood:	n/a
22	chr2:76839078-76839128	NB4	blood:	n/a
23	chr2:76839078-76839128	PANC-1	pancreas:	n/a
24	chr2:76839078-76839128	BE2_C	brain:	n/a
25	chr2:76839078-76839128	Jurkat	blood:	n/a
26	chr2:76839078-76839128	ECC-1	luminal epithelium:	n/a
27	chr2:76839078-76839128	HCPEpiC	choroid plexus:	n/a
28	chr2:76839078-76839128	AG04450	lung:	fetal
29	chr2:76839078-76839128	HCM	heart:	n/a
30	chr2:76839078-76839128	GM06990	blood:	n/a
31	chr2:76839078-76839128	MCF10A-Er-Src	breast:	n/a
32	chr2:76839078-76839128	NH-A	brain:	n/a
33	chr2:76839078-76839128	HIPEpiC	eye:	n/a
34	chr2:76839078-76839128	Hela-S3	cervix:	n/a
35	chr2:76839078-76839128	AoSMC	blood vessel:	n/a
36	chr2:76839078-76839128	AG10803	skin:	n/a
37	chr2:76839078-76839128	AG04449	skin:	fetal
38	chr2:76839078-76839128	PFSK-1	brain:	n/a
39	chr2:76839078-76839128	HCF	heart:	n/a
40	chr2:76839078-76839128	ovcar-3	ovarian:	n/a
41	chr2:76839078-76839128	GM12892	blood:	n/a
42	chr2:76839078-76839128	HNPCEpiC	eye:	n/a
43	chr2:76839078-76839128	ProgFib	skin:	n/a
44	chr2:76839078-76839128	T-47D	breast:	n/a
45	chr2:76839078-76839128	HPAEpiC	pulmonary alveolar:	n/a
46	chr2:76839078-76839128	HMEC	breast:	n/a
47	chr2:76839078-76839128	HCT-116	colon:	n/a
48	chr2:76839078-76839128	NHBE	bronchial:	n/a
49	chr2:76839078-76839128	U87	brain:	n/a
50	chr2:76839078-76839128	HL-60	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:76123697..76124563-chr2:76826531..76827162,2	MCF-7	breast:
2	chr2:76424788..76425711-chr2:76826568..76827565,9	MCF-7	breast:
3	chr2:76837968..76839669-chr2:76845469..76848246,2	MCF-7	breast:
4	chr2:76014514..76015446-chr2:76826422..76827585,4	MCF-7	breast:
5	chr2:75957100..75957649-chr2:76826627..76827405,2	MCF-7	breast:
6	chr2:76837968..76839669-chr2:76845469..76848246,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRPL19-18	chr2:76814741-76814827	NONHSAT071820
2	lnc-LRRTM4-5	chr2:76822539-76822804	NONHSAT071821

No data

Variant related genes	Relation type
RN7SKP164	TF binding region
RN7SKP164	CpG island

Extended variants
information (count: 2449 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2449 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570965923	chr2:76808471-76808472	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs539854788	chr2:76808495-76808496	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144553547	chr2:76808497-76808498	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs146635281	chr2:76808526-76808527	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141365591	chr2:76808533-76808534	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555577033	chr2:76808539-76808540	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150241570	chr2:76808611-76808612	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563667165	chr2:76808616-76808617	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138477493	chr2:76808636-76808637	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs12473223	chr2:76808645-76808646	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs564290935	chr2:76808649-76808650	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577498462	chr2:76808654-76808655	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs544631011	chr2:76808662-76808663	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559888641	chr2:76808666-76808667	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542635935	chr2:76808672-76808673	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs554565586	chr2:76808687-76808688	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573214313	chr2:76808701-76808702	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572143716	chr2:76808737-76808738	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs542364274	chr2:76808753-76808754	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189879161	chr2:76808799-76808800	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs529535608	chr2:76808820-76808821	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs540388173	chr2:76808831-76808832	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs551162767	chr2:76808838-76808839	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs11885966	chr2:76808847-76808848	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs533647789	chr2:76808859-76808860	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs551847269	chr2:76808883-76808884	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs566744718	chr2:76808893-76808894	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs369172328	chr2:76808906-76808907	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs181165569	chr2:76808911-76808912	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs534156045	chr2:76808921-76808922	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs186271034	chr2:76808939-76808940	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs116354613	chr2:76808972-76808973	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs191560677	chr2:76809004-76809005	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs183399450	chr2:76809048-76809049	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs148843234	chr2:76809078-76809079	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs188854116	chr2:76809089-76809090	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs190721470	chr2:76809093-76809094	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs532622458	chr2:76809111-76809112	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs183280470	chr2:76809136-76809137	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs116572340	chr2:76809137-76809138	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs116073005	chr2:76809161-76809162	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs143447185	chr2:76809176-76809177	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs376390287	chr2:76809183-76809184	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs563071658	chr2:76809189-76809190	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs533711768	chr2:76809193-76809194	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs371152350	chr2:76809221-76809222	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186549383	chr2:76809310-76809311	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560791733	chr2:76809340-76809341	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527699638	chr2:76809345-76809346	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548753572	chr2:76809349-76809350	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Mental retardation	17124404	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17440070	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Breast cancer	16272173	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	20531469	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:162 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:76802800-76811200	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr2:76803400-76810600	Active TSS	iPS-15b Cell Line	embryonic stem cell
3	chr2:76807000-76810200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
4	chr2:76807400-76826800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr2:76807600-76808800	Active TSS	HUES64 Cell Line	embryonic stem cell
6	chr2:76807600-76809600	Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr2:76807800-76808800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr2:76808000-76808600	Active TSS	HUES48 Cell Line	embryonic stem cell
9	chr2:76808400-76808600	Enhancers	H9 Cell Line	embryonic stem cell
10	chr2:76808600-76808800	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr2:76808600-76809200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
12	chr2:76808600-76824200	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr2:76808800-76809600	Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr2:76808800-76822200	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr2:76809200-76809800	Active TSS	HUES48 Cell Line	embryonic stem cell
16	chr2:76809600-76809800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
17	chr2:76809600-76810000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr2:76809800-76810600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
19	chr2:76809800-76811400	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr2:76810000-76810400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
21	chr2:76810200-76813600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr2:76810400-76826200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr2:76810600-76811000	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr2:76811000-76813000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr2:76811200-76813000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr2:76811400-76811800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr2:76811800-76816000	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr2:76813000-76813200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
29	chr2:76813000-76814200	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr2:76813000-76814200	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr2:76813200-76814000	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr2:76813600-76816400	Strong transcription	ES-WA7 Cell Line	embryonic stem cell
33	chr2:76814000-76817000	Strong transcription	HUES6 Cell Line	embryonic stem cell
34	chr2:76814200-76816600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr2:76814200-76826400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr2:76816000-76817000	Strong transcription	HUES48 Cell Line	embryonic stem cell
37	chr2:76816400-76817200	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
38	chr2:76816600-76817000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
39	chr2:76817000-76819200	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr2:76817000-76819400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr2:76817000-76826600	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr2:76817200-76849600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
43	chr2:76819200-76823200	Strong transcription	HUES6 Cell Line	embryonic stem cell
44	chr2:76819400-76819800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
45	chr2:76819800-76821000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr2:76821000-76823400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
47	chr2:76823200-76829400	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr2:76823400-76826800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr2:76824200-76824400	Enhancers	H9 Cell Line	embryonic stem cell
50	chr2:76824400-76825000	Enhancers	Gastric	stomach

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