Variant report

Variant	nsv1028277
Chromosome Location	chr6:57597379-58050553
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:577)
CpG islands
(count:549)
Chromatin interactive
region (count:3)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:577 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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	ATF1	chr6:57996881-57996935	K562	blood:	n/a	n/a
3	BATF	chr6:57705853-57706117	GM12878	blood:	n/a	chr6:57706041-57706049
4	BATF	chr6:57705851-57706122	GM12878	blood:	n/a	chr6:57706041-57706049
5	BCL11A	chr6:57705880-57706094	GM12878	blood:	n/a	n/a
6	BCL11A	chr6:57705843-57706108	GM12878	blood:	n/a	n/a
7	CEBPB	chr6:57837128-57837338	HepG2	liver:	n/a	chr6:57837142-57837155
8	CEBPB	chr6:58030489-58030521	HepG2	liver:	n/a	chr6:58030490-58030499 chr6:58030490-58030501 chr6:58030490-58030499 chr6:58030490-58030499 chr6:58030490-58030501 chr6:58030490-58030499
9	CEBPB	chr6:57611670-57611837	IMR90	lung:	n/a	chr6:57611723-57611734
10	CEBPB	chr6:57678653-57678665	HepG2	liver:	n/a	n/a
11	CEBPB	chr6:57835893-57836113	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr6:57813363-57813589	HepG2	liver:	n/a	chr6:57813503-57813514
13	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
14	CEBPB	chr6:57837290-57837331	A549	lung:	n/a	n/a
15	CEBPB	chr6:57813456-57813566	A549	lung:	n/a	chr6:57813503-57813514
16	CEBPB	chr6:57813381-57813566	IMR90	lung:	n/a	chr6:57813503-57813514
17	CEBPB	chr6:57611571-57611877	HepG2	liver:	n/a	chr6:57611723-57611734
18	CEBPB	chr6:57662657-57662806	HepG2	liver:	n/a	n/a
19	CEBPD	chr6:57695715-57695998	K562	blood:	n/a	n/a
20	CHD2	chr6:57757439-57757666	K562	blood:	n/a	n/a
21	CTCF	chr6:57903680-57903830	HEEpiC	esophagus:	n/a	n/a
22	CTCF	chr6:57607093-57607199	A549	lung:	n/a	n/a
23	CTCF	chr6:57726592-57726646	LNCaP	prostate:	n/a	n/a
24	CTCF	chr6:57708938-57709019	A549	lung:	n/a	chr6:57708990-57709006
25	CTCF	chr6:57903807-57904061	Medullo	brain:	n/a	chr6:57903906-57903927 chr6:57903911-57903929
26	CTCF	chr6:57903700-57903850	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr6:57726591-57726669	MCF-7	breast:	n/a	n/a
28	CTCF	chr6:57722792-57722908	ProgFib	skin:	n/a	n/a
29	CTCF	chr6:57607100-57607250	BE2_C	brain:	n/a	n/a
30	CTCF	chr6:57944165-57944201	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr6:57801044-57801048	MCF-7	breast:	n/a	n/a
32	CTCF	chr6:57754248-57754327	Spleen_OC	spleen:	n/a	n/a
33	CTCF	chr6:57689945-57690180	MCF-7	breast:	n/a	n/a
34	CTCF	chr6:57767011-57767114	K562	blood:	n/a	n/a
35	CTCF	chr6:57607001-57607267	MCF-7	breast:	n/a	n/a
36	CTCF	chr6:57766980-57767130	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr6:57607122-57607203	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr6:57689940-57690090	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr6:57689980-57690130	MCF-7	breast:	n/a	n/a
40	CTCF	chr6:57708740-57708890	GM12868	blood:	n/a	n/a
41	CTCF	chr6:57726580-57726679	MCF-7	breast:	n/a	n/a
42	CTCF	chr6:57790321-57790361	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr6:57759764-57759826	LNCaP	prostate:	n/a	n/a
44	CTCF	chr6:57778614-57778670	MCF-7	breast:	n/a	n/a
45	CTCF	chr6:57690057-57690127	GM19238	blood:	n/a	n/a
46	CTCF	chr6:57778604-57778613	MCF-7	breast:	n/a	n/a
47	CTCF	chr6:57811435-57811642	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr6:57754509-57754609	GM12892	blood:	n/a	n/a
49	CTCF	chr6:57678235-57678311	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:57791167-57791299	Lung_OC	lung:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:58001971-58002021	GM19239	blood:	n/a
2	chr6:57972349-57972399	H1-hESC	embryonic stem cell:	embryo
3	chr6:57970592-57970642	HMEC	breast:	n/a
4	chr6:57614321-57614371	AG09319	gingival:	n/a
5	chr6:57972680-57972730	HCM	heart:	n/a
6	chr6:57972349-57972399	HMEC	breast:	n/a
7	chr6:57912662-57912712	SK-N-MC	brain:	n/a
8	chr6:57970592-57970642	HIPEpiC	eye:	n/a
9	chr6:57972223-57972273	NHBE	bronchial:	n/a
10	chr6:57970666-57970716	HEEpiC	esophagus:	n/a
11	chr6:57972223-57972273	PFSK-1	brain:	n/a
12	chr6:57614321-57614371	Jurkat	blood:	n/a
13	chr6:57972721-57972771	U87	brain:	n/a
14	chr6:57972680-57972730	NHBE	bronchial:	n/a
15	chr6:57970592-57970642	K562	blood:	n/a
16	chr6:57972721-57972771	HCT-116	colon:	n/a
17	chr6:57970666-57970716	RPTEC	kidney:	n/a
18	chr6:57970592-57970642	A549	lung:	n/a
19	chr6:57972223-57972273	AG04450	lung:	fetal
20	chr6:57912662-57912712	HAEpiC	amniotic membrane:	n/a
21	chr6:57972680-57972730	SK-N-SH_RA	brain:	n/a
22	chr6:57970666-57970716	NB4	blood:	n/a
23	chr6:57972721-57972771	Jurkat	blood:	n/a
24	chr6:57970592-57970642	HPAEpiC	pulmonary alveolar:	n/a
25	chr6:57972349-57972399	SK-N-SH	brain:	n/a
26	chr6:57970592-57970642	Hela-S3	cervix:	n/a
27	chr6:57912662-57912712	MCF-7	breast:	n/a
28	chr6:57970666-57970716	SKMC	muscle:	n/a
29	chr6:57614321-57614371	HPAEpiC	pulmonary alveolar:	n/a
30	chr6:57972721-57972771	HL-60	blood:	n/a
31	chr6:57972223-57972273	AG04449	skin:	fetal
32	chr6:57970592-57970642	SKMC	muscle:	n/a
33	chr6:57970592-57970642	IMR90	lung:	fetal
34	chr6:58001971-58002021	SK-N-SH_RA	brain:	n/a
35	chr6:57972721-57972771	A549	lung:	n/a
36	chr6:57972349-57972399	HepG2	liver:	n/a
37	chr6:57972721-57972771	GM12878	blood:	n/a
38	chr6:57912662-57912712	ECC-1	luminal epithelium:	n/a
39	chr6:57972349-57972399	AG09319	gingival:	n/a
40	chr6:57972680-57972730	SK-N-MC	brain:	n/a
41	chr6:57970592-57970642	Caco-2	colon:	n/a
42	chr6:57970666-57970716	BJ	skin:	n/a
43	chr6:57912662-57912712	HEEpiC	esophagus:	n/a
44	chr6:57614321-57614371	HEK293	kidney:	embryo
45	chr6:57972223-57972273	SKMC	muscle:	n/a
46	chr6:57970666-57970716	PrEC	prostate:	n/a
47	chr6:57912662-57912712	HCT-116	colon:	n/a
48	chr6:57972223-57972273	GM06990	blood:	n/a
49	chr6:58001971-58002021	HRE	kidney:	n/a
50	chr6:57972223-57972273	HL-60	blood:	n/a

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

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

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

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

No data

Variant related genes	Relation type
ENSG00000270213	TF binding region
ENSG00000231273	TF binding region
GAPDHP41	TF binding region
RBBP4P3	TF binding region
ENSG00000262828	TF binding region
ENSG00000270213	CpG island
ENSG00000231273	CpG island
GAPDHP41	CpG island
RBBP4P3	CpG island
ENSG00000262828	CpG island
NR3C1	miRNA target sites
PNN	miRNA target sites

Extended variants
information (count: 3690 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:3690 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs66670873	chr6:57604009-57604010	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs377204786	chr6:57604036-57604037	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs75391884	chr6:57604043-57604044	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs79057469	chr6:57604046-57604047	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs35450217	chr6:57604079-57604080	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs146034791	chr6:57604085-57604086	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs6906898	chr6:57604087-57604088	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs36190183	chr6:57604096-57604097	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs558350601	chr6:57604109-57604110	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs73459253	chr6:57604135-57604136	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs570276029	chr6:57604156-57604157	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs184313332	chr6:57604159-57604160	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs534804310	chr6:57604190-57604191	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs35362605	chr6:57604218-57604219	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs530217726	chr6:57604221-57604222	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs553004814	chr6:57604238-57604239	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs62411880	chr6:57604253-57604254	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs376302450	chr6:57604255-57604256	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs113823046	chr6:57604274-57604275	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs79483690	chr6:57604275-57604276	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs398094240	chr6:57604277-57604278	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs61358066	chr6:57604296-57604297	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs201953218	chr6:57604318-57604319	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs62411881	chr6:57604319-57604320	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs542253054	chr6:57604337-57604338	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs111757343	chr6:57604339-57604340	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs557063450	chr6:57604349-57604350	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs575922081	chr6:57604358-57604359	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs546492884	chr6:57604363-57604364	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs141266160	chr6:57604394-57604395	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs73756287	chr6:57606223-57606224	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs73756288	chr6:57606245-57606246	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs9396394	chr6:57606251-57606252	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs544460373	chr6:57606283-57606284	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs562681467	chr6:57606285-57606286	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs73459272	chr6:57606292-57606293	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs533112461	chr6:57606305-57606306	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs73459273	chr6:57606319-57606320	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs545220388	chr6:57606323-57606324	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs74435498	chr6:57606342-57606343	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs145449351	chr6:57606344-57606345	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs113893201	chr6:57606345-57606346	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs113506204	chr6:57606348-57606349	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs77568934	chr6:57606365-57606366	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs77296684	chr6:57606380-57606381	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs113473172	chr6:57606386-57606387	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs560610881	chr6:57606400-57606401	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs527771437	chr6:57606405-57606406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73459275	chr6:57606418-57606419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs35137437	chr6:57606435-57606436	Weak transcription	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:178 , 50 per page) page: 1 2 3 4

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

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