Variant report

Variant	nsv1018575
Chromosome Location	chr6:57596090-57911812
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:503)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:503 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:57618389-57618391	K562	blood:	n/a	n/a
2	BATF	chr6:57705851-57706122	GM12878	blood:	n/a	chr6:57706041-57706049
3	BATF	chr6:57705853-57706117	GM12878	blood:	n/a	chr6:57706041-57706049
4	BCL11A	chr6:57705843-57706108	GM12878	blood:	n/a	n/a
5	BCL11A	chr6:57705880-57706094	GM12878	blood:	n/a	n/a
6	CEBPB	chr6:57678625-57678743	K562	blood:	n/a	chr6:57678645-57678662 chr6:57678650-57678661 chr6:57678648-57678661 chr6:57678648-57678659 chr6:57678648-57678661 chr6:57678650-57678661
7	CEBPB	chr6:57611670-57611837	IMR90	lung:	n/a	chr6:57611723-57611734
8	CEBPB	chr6:57835893-57836113	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr6:57813456-57813566	A549	lung:	n/a	chr6:57813503-57813514
10	CEBPB	chr6:57837290-57837331	A549	lung:	n/a	n/a
11	CEBPB	chr6:57837128-57837338	HepG2	liver:	n/a	chr6:57837142-57837155
12	CEBPB	chr6:57611571-57611877	HepG2	liver:	n/a	chr6:57611723-57611734
13	CEBPB	chr6:57662657-57662806	HepG2	liver:	n/a	n/a
14	CEBPB	chr6:57813363-57813589	HepG2	liver:	n/a	chr6:57813503-57813514
15	CEBPB	chr6:57813381-57813566	IMR90	lung:	n/a	chr6:57813503-57813514
16	CEBPB	chr6:57678653-57678665	HepG2	liver:	n/a	n/a
17	CEBPD	chr6:57695715-57695998	K562	blood:	n/a	n/a
18	CHD2	chr6:57757439-57757666	K562	blood:	n/a	n/a
19	CTCF	chr6:57726580-57726679	MCF-7	breast:	n/a	n/a
20	CTCF	chr6:57607105-57607182	Fibrobl	skin:	n/a	n/a
21	CTCF	chr6:57722760-57722910	SAEC	small airway:	n/a	n/a
22	CTCF	chr6:57754248-57754327	Spleen_OC	spleen:	n/a	n/a
23	CTCF	chr6:57722820-57722876	GM19239	blood:	n/a	n/a
24	CTCF	chr6:57722733-57722918	Pancreas_OC	pancreas:	n/a	n/a
25	CTCF	chr6:57689967-57690149	HepG2	liver:	n/a	n/a
26	CTCF	chr6:57791327-57791426	Medullo	brain:	n/a	n/a
27	CTCF	chr6:57767033-57767131	Fibrobl	skin:	n/a	n/a
28	CTCF	chr6:57666168-57666243	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr6:57690027-57690145	A549	lung:	n/a	n/a
30	CTCF	chr6:57754541-57754609	GM12878	blood:	n/a	n/a
31	CTCF	chr6:57689960-57690110	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr6:57689391-57689423	LNCaP	prostate:	n/a	n/a
33	CTCF	chr6:57811475-57811593	GM12891	blood:	n/a	n/a
34	CTCF	chr6:57754538-57754610	LNCaP	prostate:	n/a	n/a
35	CTCF	chr6:57811420-57811570	HEEpiC	esophagus:	n/a	chr6:57811427-57811440
36	CTCF	chr6:57766980-57767130	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr6:57722760-57722910	HMEC	breast:	n/a	n/a
38	CTCF	chr6:57689991-57690112	GM19239	blood:	n/a	n/a
39	CTCF	chr6:57903824-57904064	K562	blood:	n/a	chr6:57903906-57903927 chr6:57903911-57903929
40	CTCF	chr6:57722789-57722899	NHEK	skin:	n/a	n/a
41	CTCF	chr6:57767080-57767230	HEK293	kidney:	n/a	chr6:57767195-57767203
42	CTCF	chr6:57903580-57903730	HMEC	breast:	n/a	n/a
43	CTCF	chr6:57811400-57811550	WERI-Rb-1	eye:	n/a	chr6:57811427-57811440
44	CTCF	chr6:57629486-57629578	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr6:57607000-57607150	HEK293	kidney:	n/a	n/a
46	CTCF	chr6:57722680-57722830	HMEC	breast:	n/a	n/a
47	CTCF	chr6:57690057-57690127	GM19238	blood:	n/a	n/a
48	CTCF	chr6:57722799-57722887	Fibrobl	skin:	n/a	n/a
49	CTCF	chr6:57766987-57767126	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chr6:57811435-57811642	Pancreas_OC	pancreas:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:57614321-57614371	ProgFib	skin:	n/a
2	chr6:57614321-57614371	AoSMC	blood vessel:	n/a
3	chr6:57614321-57614371	SK-N-SH	brain:	n/a
4	chr6:57614321-57614371	MCF-7	breast:	n/a
5	chr6:57614321-57614371	NT2-D1	testis:	n/a
6	chr6:57614321-57614371	T-47D	breast:	n/a
7	chr6:57614321-57614371	Hela-S3	cervix:	n/a
8	chr6:57614321-57614371	H1-hESC	embryonic stem cell:	embryo
9	chr6:57614321-57614371	AG10803	skin:	n/a
10	chr6:57614321-57614371	U87	brain:	n/a
11	chr6:57614321-57614371	GM19239	blood:	n/a
12	chr6:57614321-57614371	HRE	kidney:	n/a
13	chr6:57614321-57614371	HepG2	liver:	n/a
14	chr6:57614321-57614371	PrEC	prostate:	n/a
15	chr6:57614321-57614371	PANC-1	pancreas:	n/a
16	chr6:57614321-57614371	HL-60	blood:	n/a
17	chr6:57614321-57614371	SK-N-SH_RA	brain:	n/a
18	chr6:57614321-57614371	ECC-1	luminal epithelium:	n/a
19	chr6:57614321-57614371	HCM	heart:	n/a
20	chr6:57614321-57614371	HAEpiC	amniotic membrane:	n/a
21	chr6:57614321-57614371	HCF	heart:	n/a
22	chr6:57614321-57614371	NHBE	bronchial:	n/a
23	chr6:57614321-57614371	GM12891	blood:	n/a
24	chr6:57614321-57614371	A549	lung:	n/a
25	chr6:57614321-57614371	HRCEpiC	kidney:	n/a
26	chr6:57614321-57614371	GM12892	blood:	n/a
27	chr6:57614321-57614371	BE2_C	brain:	n/a
28	chr6:57614321-57614371	NB4	blood:	n/a
29	chr6:57614321-57614371	SKMC	muscle:	n/a
30	chr6:57614321-57614371	NH-A	brain:	n/a
31	chr6:57614321-57614371	HIPEpiC	eye:	n/a
32	chr6:57614321-57614371	HEEpiC	esophagus:	n/a
33	chr6:57614321-57614371	SAEC	small airway:	n/a
34	chr6:57614321-57614371	K562	blood:	n/a
35	chr6:57614321-57614371	HRPEpiC	eye:	n/a
36	chr6:57614321-57614371	HEK293	kidney:	embryo
37	chr6:57614321-57614371	HCT-116	colon:	n/a
38	chr6:57614321-57614371	AG04450	lung:	fetal
39	chr6:57614321-57614371	HCPEpiC	choroid plexus:	n/a
40	chr6:57614321-57614371	Caco-2	colon:	n/a
41	chr6:57614321-57614371	Hepatocyte	liver:	n/a
42	chr6:57614321-57614371	BJ	skin:	n/a
43	chr6:57614321-57614371	MCF10A-Er-Src	breast:	n/a
44	chr6:57614321-57614371	GM12878	blood:	n/a
45	chr6:57614321-57614371	LNCaP	prostate:	n/a
46	chr6:57614321-57614371	PFSK-1	brain:	n/a
47	chr6:57614321-57614371	AG09309	skin:	n/a
48	chr6:57614321-57614371	IMR90	lung:	fetal
49	chr6:57614321-57614371	SK-N-MC	brain:	n/a
50	chr6:57614321-57614371	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr6:57766644..57767228-chr6:62859661..62860581,2	MCF-7	breast:
2	chr6:57445356..57445958-chr6:57689666..57690275,2	MCF-7	breast:
3	chr11:17753668..17754453-chr6:57615850..57616702,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAB23-13	chr6:57671339-57671489	NONHSAT113298
2	lnc-BAG2-11	chr6:57798854-57798915	NONHSAT113302
3	lnc-RAB23-15	chr6:57793932-57794280	NONHSAT113301
4	lnc-RAB23-14	chr6:57686969-57687949	NONHSAT113299
5	lnc-BAG2-11	chr6:57799352-57799604	NONHSAT113302
6	lnc-RAB23-13	chr6:57674277-57674350	NONHSAT113298
7	lnc-BAG2-3	chr6:57691393-57691645	XLOC_005331
8	lnc-BAG2-3	chr6:57690895-57690956	XLOC_005331

No data

Variant related genes	Relation type
ENSG00000231273	TF binding region
GAPDHP41	TF binding region
RBBP4P3	TF binding region
ENSG00000262828	TF binding region
ENSG00000231273	CpG island
GAPDHP41	CpG island
RBBP4P3	CpG island
ENSG00000262828	CpG island
PNN	miRNA target sites
NR3C1	miRNA target sites

Extended variants
information (count: 3334 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:3334 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78210211	chr6:57596606-57596607	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs75138641	chr6:57596612-57596613	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs79850934	chr6:57596613-57596614	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs566082624	chr6:57596637-57596638	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs386701730	chr6:57596639-57596640	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs77603077	chr6:57596640-57596641	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs536215157	chr6:57596642-57596643	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs72871592	chr6:57596649-57596650	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs35925128	chr6:57596656-57596657	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs73457558	chr6:57596683-57596684	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs75145795	chr6:57596715-57596716	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs386701731	chr6:57596720-57596721	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs79946698	chr6:57596721-57596722	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs76799084	chr6:57596729-57596730	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs367648533	chr6:57596735-57596736	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs570057476	chr6:57596739-57596740	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs537335954	chr6:57596740-57596741	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs58673413	chr6:57596761-57596762	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs577343367	chr6:57596762-57596763	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs141223972	chr6:57596764-57596765	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs553551370	chr6:57596776-57596777	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs73457564	chr6:57596781-57596782	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs572016137	chr6:57596787-57596788	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs9464557	chr6:57596792-57596793	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs146121094	chr6:57596793-57596794	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs28409504	chr6:57596814-57596815	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs79496157	chr6:57596831-57596832	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs73457566	chr6:57596837-57596838	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs576439322	chr6:57596845-57596846	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs543720319	chr6:57596874-57596875	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs73457570	chr6:57596891-57596892	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs34762248	chr6:57596903-57596904	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs377261833	chr6:57596927-57596928	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs73457573	chr6:57596940-57596941	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs76390453	chr6:57596945-57596946	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs547880573	chr6:57596999-57597000	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs66670873	chr6:57604009-57604010	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs377204786	chr6:57604036-57604037	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs75391884	chr6:57604043-57604044	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs79057469	chr6:57604046-57604047	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs35450217	chr6:57604079-57604080	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs146034791	chr6:57604085-57604086	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs6906898	chr6:57604087-57604088	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs36190183	chr6:57604096-57604097	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs558350601	chr6:57604109-57604110	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs73459253	chr6:57604135-57604136	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs570276029	chr6:57604156-57604157	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs184313332	chr6:57604159-57604160	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs534804310	chr6:57604190-57604191	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs35362605	chr6:57604218-57604219	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Neuroblastoma	16790693	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
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Glioma	20126413	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:143 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:57596600-57597000	Active TSS	Aorta	Aorta
2	chr6:57604000-57604400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
3	chr6:57606200-57606400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr6:57606400-57616600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr6:57607200-57611400	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr6:57614000-57614600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr6:57614400-57615200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr6:57634000-57637800	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr6:57635400-57635600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:57635600-57642400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr6:57635800-57636200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
12	chr6:57636200-57637200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr6:57636800-57641800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr6:57637200-57640400	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr6:57637400-57638600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr6:57637600-57640200	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr6:57637800-57638200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr6:57637800-57638600	Enhancers	H9 Cell Line	embryonic stem cell
19	chr6:57637800-57638600	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr6:57637800-57638800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr6:57637800-57639000	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr6:57637800-57640800	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr6:57638000-57639600	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr6:57638600-57639600	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr6:57638800-57639200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
26	chr6:57639000-57641800	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr6:57639200-57640800	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr6:57640000-57640200	Enhancers	H9 Cell Line	embryonic stem cell
29	chr6:57640200-57642000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr6:57640800-57642800	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr6:57641800-57642200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr6:57641800-57642200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
33	chr6:57642000-57643600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
34	chr6:57642800-57643400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
35	chr6:57646800-57647000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr6:57647600-57648600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr6:57648600-57649000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr6:57649000-57652400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr6:57649600-57649800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr6:57650200-57653800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr6:57653200-57655600	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr6:57653600-57655600	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr6:57653800-57654600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr6:57654200-57655600	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr6:57655000-57655600	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr6:57655200-57655600	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr6:57655600-57659000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr6:57655600-57659000	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr6:57659000-57659400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr6:57659000-57659400	Enhancers	HUES48 Cell Line	embryonic stem cell

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