Variant report

Variant	nsv970096
Chromosome Location	chr6:28927690-28939080
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:174)
CpG islands
(count:122)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:174 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:28928928-28928962	K562	blood:	n/a	n/a
2	ATF1	chr6:28933523-28933707	K562	blood:	n/a	n/a
3	ATF1	chr6:28928793-28929120	K562	blood:	n/a	n/a
4	BACH1	chr6:28928912-28929044	K562	blood:	n/a	n/a
5	BHLHE40	chr6:28928828-28929147	K562	blood:	n/a	n/a
6	CBX3	chr6:28927944-28929601	K562	blood:	n/a	n/a
7	CBX3	chr6:28936470-28936863	K562	blood:	n/a	n/a
8	CBX3	chr6:28936292-28937388	K562	blood:	n/a	n/a
9	CEBPB	chr6:28928854-28928861	K562	blood:	n/a	n/a
10	CEBPB	chr6:28939053-28939205	HepG2	liver:	n/a	n/a
11	CEBPD	chr6:28928620-28929126	K562	blood:	n/a	n/a
12	CHD2	chr6:28928758-28929086	K562	blood:	n/a	n/a
13	CTCF	chr6:28936860-28937010	BJ	skin:	n/a	n/a
14	CTCF	chr6:28936940-28937090	A549	lung:	n/a	n/a
15	CTCF	chr6:28937169-28937174	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr6:28930400-28930439	LNCaP	prostate:	n/a	n/a
17	CTCF	chr6:28936880-28937030	HUVEC	blood vessel:	n/a	n/a
18	CTCF	chr6:28936980-28937130	A549	lung:	n/a	n/a
19	CTCF	chr6:28936880-28937030	WI-38	lung:	n/a	n/a
20	CTCF	chr6:28936980-28937130	BE2_C	brain:	n/a	n/a
21	CTCF	chr6:28937000-28937150	HRE	kidney:	n/a	n/a
22	CTCF	chr6:28936869-28937209	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr6:28937060-28937210	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr6:28936920-28937168	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr6:28936980-28937130	HVMF	connective:	n/a	n/a
26	CTCF	chr6:28937011-28937104	A549	lung:	n/a	n/a
27	CTCF	chr6:28936969-28937172	Fibrobl	skin:	n/a	n/a
28	CTCF	chr6:28936940-28937090	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr6:28936966-28937122	ProgFib	skin:	n/a	n/a
30	CTCF	chr6:28936960-28937110	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr6:28936980-28937130	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr6:28937039-28937046	Gliobla	brain:	n/a	n/a
33	CTCF	chr6:28929290-28929341	GM20000	blood:	n/a	n/a
34	CTCF	chr6:28936960-28937110	HepG2	liver:	n/a	n/a
35	CTCF	chr6:28936992-28937133	NHEK	skin:	n/a	n/a
36	CTCF	chr6:28936920-28937070	HMF	breast:	n/a	n/a
37	CTCF	chr6:28936980-28937130	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr6:28936941-28937204	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr6:28936963-28937121	A549	lung:	n/a	n/a
40	CTCF	chr6:28936900-28937050	HFF-Myc	foreskin:	n/a	n/a
41	CTCF	chr6:28937008-28937116	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr6:28929160-28929310	HEK293	kidney:	n/a	n/a
43	CTCF	chr6:28936960-28937110	HMEC	breast:	n/a	n/a
44	CTCF	chr6:28936920-28937070	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr6:28936896-28937157	K562	blood:	n/a	n/a
46	CTCF	chr6:28936997-28937135	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr6:28936980-28937130	SAEC	small airway:	n/a	n/a
48	CTCF	chr6:28937020-28937170	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr6:28937044-28937095	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:28937069-28937075	Gliobla	brain:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:28937310-28937360	HCF	heart:	n/a
2	chr6:28937310-28937360	ProgFib	skin:	n/a
3	chr6:28937310-28937360	RPTEC	kidney:	n/a
4	chr6:28938132-28938182	NHBE	bronchial:	n/a
5	chr6:28937310-28937360	AG04449	skin:	fetal
6	chr6:28938132-28938182	IMR90	lung:	fetal
7	chr6:28938132-28938182	SK-N-SH_RA	brain:	n/a
8	chr6:28937310-28937360	BE2_C	brain:	n/a
9	chr6:28938132-28938182	NHDF-neo	bronchial:	n/a
10	chr6:28938132-28938182	HMEC	breast:	n/a
11	chr6:28938132-28938182	AG04449	skin:	fetal
12	chr6:28937310-28937360	HepG2	liver:	n/a
13	chr6:28937310-28937360	NT2-D1	testis:	n/a
14	chr6:28938132-28938182	ECC-1	luminal epithelium:	n/a
15	chr6:28937310-28937360	AG09319	gingival:	n/a
16	chr6:28937310-28937360	HNPCEpiC	eye:	n/a
17	chr6:28937310-28937360	ovcar-3	ovarian:	n/a
18	chr6:28938132-28938182	HCT-116	colon:	n/a
19	chr6:28938132-28938182	AoSMC	blood vessel:	n/a
20	chr6:28938132-28938182	HCF	heart:	n/a
21	chr6:28938132-28938182	LNCaP	prostate:	n/a
22	chr6:28937310-28937360	CMK	blood:	n/a
23	chr6:28938132-28938182	GM06990	blood:	n/a
24	chr6:28938132-28938182	HRPEpiC	eye:	n/a
25	chr6:28938132-28938182	HRE	kidney:	n/a
26	chr6:28937310-28937360	SK-N-MC	brain:	n/a
27	chr6:28938132-28938182	H1-hESC	embryonic stem cell:	embryo
28	chr6:28937310-28937360	U87	brain:	n/a
29	chr6:28937310-28937360	NHDF-neo	bronchial:	n/a
30	chr6:28938132-28938182	HCPEpiC	choroid plexus:	n/a
31	chr6:28938132-28938182	MCF-7	breast:	n/a
32	chr6:28937310-28937360	NH-A	brain:	n/a
33	chr6:28937310-28937360	HRPEpiC	eye:	n/a
34	chr6:28938132-28938182	K562	blood:	n/a
35	chr6:28938132-28938182	GM12878	blood:	n/a
36	chr6:28938132-28938182	RPTEC	kidney:	n/a
37	chr6:28937310-28937360	MCF-7	breast:	n/a
38	chr6:28937310-28937360	AG10803	skin:	n/a
39	chr6:28938132-28938182	AG09309	skin:	n/a
40	chr6:28938132-28938182	Hela-S3	cervix:	n/a
41	chr6:28937310-28937360	AG04450	lung:	fetal
42	chr6:28937310-28937360	K562	blood:	n/a
43	chr6:28938132-28938182	ProgFib	skin:	n/a
44	chr6:28938132-28938182	CMK	blood:	n/a
45	chr6:28937310-28937360	Caco-2	colon:	n/a
46	chr6:28938132-28938182	GM19239	blood:	n/a
47	chr6:28937310-28937360	T-47D	breast:	n/a
48	chr6:28938132-28938182	BE2_C	brain:	n/a
49	chr6:28937310-28937360	SAEC	small airway:	n/a
50	chr6:28938132-28938182	NB4	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:28926644..28928664-chr6:28929682..28931207,2	K562	blood:
2	chr6:28926004..28928309-chr6:28944355..28946221,2	K562	blood:
3	chr6:28888002..28892936-chr6:28927795..28931066,4	K562	blood:
4	chr6:28926644..28928664-chr6:28929682..28931207,2	K562	blood:
5	chr6:28928142..28929743-chr6:28947588..28949383,2	K562	blood:
6	chr6:28916396..28919032-chr6:28931395..28932899,2	K562	blood:
7	chr6:28889372..28892274-chr6:28936954..28941148,4	K562	blood:
8	chr6:28926644..28928695-chr6:28929682..28932327,2	K562	blood:
9	chr6:28926644..28928695-chr6:28929682..28932327,2	K562	blood:
10	chr6:28887886..28894013-chr6:28935014..28940220,8	K562	blood:
11	chr6:28926035..28928870-chr6:28956157..28957921,2	K562	blood:
12	chr6:28931535..28933777-chr6:28950543..28952333,2	K562	blood:
13	chr6:28927503..28930873-chr6:28944812..28947350,3	K562	blood:
14	chr6:28890252..28892936-chr6:28929297..28931066,2	K562	blood:
15	chr6:28931828..28934323-chr6:28943068..28945762,2	K562	blood:

No data

Variant related genes	Relation type
KRT18P1	TF binding region
KRT18P1	CpG island
ENSG00000204713	chromatin interactions
ENSG00000263426	chromatin interactions

Extended variants
information (count: 400 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:400 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560751230	chr6:28927719-28927720	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs574347776	chr6:28927744-28927745	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs142970597	chr6:28927749-28927750	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs68123503	chr6:28927750-28927751	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs33959457	chr6:28927751-28927752	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs543139844	chr6:28927752-28927753	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs386487580	chr6:28927753-28927754	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs540173587	chr6:28927766-28927767	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs370219549	chr6:28927774-28927775	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs564263606	chr6:28927781-28927782	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs373973738	chr6:28927833-28927834	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs7763905	chr6:28927864-28927865	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs149249130	chr6:28927868-28927869	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs562333102	chr6:28927876-28927877	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs184269778	chr6:28927908-28927909	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs563889279	chr6:28927931-28927932	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs373251958	chr6:28927932-28927933	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs188552195	chr6:28927973-28927974	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs180919181	chr6:28927991-28927992	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs370458524	chr6:28928005-28928006	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs375729752	chr6:28928009-28928010	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs567202688	chr6:28928018-28928019	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs528092420	chr6:28928020-28928021	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs539334371	chr6:28928035-28928036	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs185905514	chr6:28928049-28928050	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs569453513	chr6:28928060-28928061	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs537961754	chr6:28928062-28928063	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs554616003	chr6:28928063-28928064	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs574359498	chr6:28928083-28928084	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs540178903	chr6:28928106-28928107	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs553484059	chr6:28928111-28928112	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs576767564	chr6:28928124-28928125	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs12386522	chr6:28928167-28928168	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs562360154	chr6:28928178-28928179	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs374243347	chr6:28928197-28928198	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs144480264	chr6:28928198-28928199	Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs189169292	chr6:28928206-28928207	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs137937474	chr6:28928236-28928237	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs182568447	chr6:28928244-28928245	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs368835890	chr6:28928245-28928246	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs547015732	chr6:28928278-28928279	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs187139040	chr6:28928308-28928309	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs532884959	chr6:28928324-28928325	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs190610466	chr6:28928333-28928334	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs182786457	chr6:28928335-28928336	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs377654472	chr6:28928418-28928419	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs142519937	chr6:28928437-28928438	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs538401896	chr6:28928465-28928466	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs372763052	chr6:28928467-28928468	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs554369647	chr6:28928485-28928486	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
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
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:28922200-28928400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:28922200-28930600	Weak transcription	Right Atrium	heart
3	chr6:28923000-28928600	Weak transcription	HepG2	liver
4	chr6:28923400-28928600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr6:28923800-28928600	Weak transcription	NHEK	skin
6	chr6:28927000-28928000	Enhancers	K562	blood
7	chr6:28928000-28929400	Flanking Active TSS	K562	blood
8	chr6:28928200-28929400	Enhancers	Hela-S3	cervix
9	chr6:28928400-28928800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr6:28928400-28929200	Enhancers	Stomach Mucosa	stomach
11	chr6:28928600-28928800	Enhancers	HepG2	liver
12	chr6:28928600-28929000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr6:28928600-28929000	Enhancers	HMEC	breast
14	chr6:28928600-28929200	Enhancers	NHEK	skin
15	chr6:28928800-28929200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr6:28929000-28929400	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr6:28929400-28929600	Enhancers	K562	blood
18	chr6:28929600-28932800	Weak transcription	K562	blood
19	chr6:28932800-28933600	Enhancers	K562	blood
20	chr6:28933600-28936000	Weak transcription	K562	blood
21	chr6:28936000-28936800	ZNF genes & repeats	K562	blood
22	chr6:28936800-28937800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr6:28937800-28944800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr6:28938400-28938800	Enhancers	HepG2	liver
25	chr6:28938800-28941800	Weak transcription	HepG2	liver

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