Variant report

Variant	nsv981564
Chromosome Location	chr7:102704804-102712972
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:231)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:231 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:102706276-102706354	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr7:102706243-102706451	K562	blood:	n/a	n/a
3	CTCF	chr7:102706220-102706370	HBMEC	blood vessel:	n/a	n/a
4	CTCF	chr7:102706240-102706390	GM06990	blood:	n/a	n/a
5	CTCF	chr7:102706100-102706250	HAc	cerebellar:	n/a	n/a
6	CTCF	chr7:102706220-102706370	GM12870	blood:	n/a	n/a
7	CTCF	chr7:102706240-102706390	AoAF	blood vessel:	n/a	n/a
8	CTCF	chr7:102705886-102706593	SK-N-SH	brain:	n/a	n/a
9	CTCF	chr7:102706240-102706390	GM12872	blood:	n/a	n/a
10	CTCF	chr7:102706143-102706424	HepG2	liver:	n/a	n/a
11	CTCF	chr7:102706135-102706431	K562	blood:	n/a	n/a
12	CTCF	chr7:102706240-102706390	HCT-116	colon:	n/a	n/a
13	CTCF	chr7:102706238-102706376	Pancreas_OC	pancreas:	n/a	n/a
14	CTCF	chr7:102706179-102706479	MCF-7	breast:	n/a	n/a
15	CTCF	chr7:102706260-102706410	HRE	kidney:	n/a	n/a
16	CTCF	chr7:102706176-102706439	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr7:102706300-102706450	HMEC	breast:	n/a	n/a
18	CTCF	chr7:102706240-102706390	GM12869	blood:	n/a	n/a
19	CTCF	chr7:102706260-102706410	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr7:102706240-102706390	GM12875	blood:	n/a	n/a
21	CTCF	chr7:102706220-102706370	NB4	blood:	n/a	n/a
22	CTCF	chr7:102706158-102706485	MCF-7	breast:	n/a	n/a
23	CTCF	chr7:102706139-102706498	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr7:102706114-102706507	K562	blood:	n/a	n/a
25	CTCF	chr7:102706159-102706464	Gliobla	brain:	n/a	n/a
26	CTCF	chr7:102707924-102707944	GM20000	blood:	n/a	n/a
27	CTCF	chr7:102706220-102706370	HAc	cerebellar:	n/a	n/a
28	CTCF	chr7:102706240-102706390	HepG2	liver:	n/a	n/a
29	CTCF	chr7:102706240-102706390	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr7:102706240-102706390	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr7:102706240-102706390	BJ	skin:	n/a	n/a
32	CTCF	chr7:102706220-102706370	HFF	foreskin:	n/a	n/a
33	CTCF	chr7:102706180-102706330	K562	blood:	n/a	n/a
34	CTCF	chr7:102706240-102706390	AG04450	lung:	n/a	n/a
35	CTCF	chr7:102706200-102706350	NHDF-neo	bronchial:	n/a	n/a
36	CTCF	chr7:102706077-102706497	HepG2	liver:	n/a	n/a
37	CTCF	chr7:102705983-102706674	A549	lung:	n/a	n/a
38	CTCF	chr7:102706211-102706432	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr7:102706026-102706630	MCF-7	breast:	n/a	n/a
40	CTCF	chr7:102706220-102706370	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr7:102706220-102706370	GM12875	blood:	n/a	n/a
42	CTCF	chr7:102706260-102706410	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr7:102706173-102706457	GM19240	blood:	n/a	n/a
44	CTCF	chr7:102706220-102706370	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr7:102706180-102706330	BE2_C	brain:	n/a	n/a
46	CTCF	chr7:102706181-102706474	A549	lung:	n/a	n/a
47	CTCF	chr7:102706045-102706603	MCF-7	breast:	n/a	n/a
48	CTCF	chr7:102706157-102706458	GM19239	blood:	n/a	n/a
49	CTCF	chr7:102706166-102706530	A549	lung:	n/a	n/a
50	CTCF	chr7:102706220-102706370	GM12873	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102711687-102711737	Jurkat	blood:	n/a
2	chr7:102711687-102711737	HIPEpiC	eye:	n/a
3	chr7:102711687-102711737	ECC-1	luminal epithelium:	n/a
4	chr7:102711687-102711737	HL-60	blood:	n/a
5	chr7:102711687-102711737	NB4	blood:	n/a
6	chr7:102711687-102711737	PFSK-1	brain:	n/a
7	chr7:102711687-102711737	HUVEC	blood vessel:	n/a
8	chr7:102711687-102711737	GM12891	blood:	n/a
9	chr7:102711687-102711737	PANC-1	pancreas:	n/a
10	chr7:102711687-102711737	ovcar-3	ovarian:	n/a
11	chr7:102711687-102711737	HNPCEpiC	eye:	n/a
12	chr7:102711687-102711737	A549	lung:	n/a
13	chr7:102711687-102711737	T-47D	breast:	n/a
14	chr7:102711687-102711737	LNCaP	prostate:	n/a
15	chr7:102711687-102711737	Hepatocyte	liver:	n/a
16	chr7:102711687-102711737	AoSMC	blood vessel:	n/a
17	chr7:102711687-102711737	HEEpiC	esophagus:	n/a
18	chr7:102711687-102711737	NT2-D1	testis:	n/a
19	chr7:102711687-102711737	GM12878	blood:	n/a
20	chr7:102711687-102711737	GM12892	blood:	n/a
21	chr7:102711687-102711737	AG09309	skin:	n/a
22	chr7:102711687-102711737	SK-N-SH	brain:	n/a
23	chr7:102711687-102711737	BJ	skin:	n/a
24	chr7:102711687-102711737	AG10803	skin:	n/a
25	chr7:102711687-102711737	HCF	heart:	n/a
26	chr7:102711687-102711737	HAEpiC	amniotic membrane:	n/a
27	chr7:102711687-102711737	Hela-S3	cervix:	n/a
28	chr7:102711687-102711737	MCF10A-Er-Src	breast:	n/a
29	chr7:102711687-102711737	BE2_C	brain:	n/a
30	chr7:102711687-102711737	HRE	kidney:	n/a
31	chr7:102711687-102711737	PrEC	prostate:	n/a
32	chr7:102711687-102711737	RPTEC	kidney:	n/a
33	chr7:102711687-102711737	IMR90	lung:	fetal
34	chr7:102711687-102711737	HMEC	breast:	n/a
35	chr7:102711687-102711737	SK-N-SH_RA	brain:	n/a
36	chr7:102711687-102711737	SKMC	muscle:	n/a
37	chr7:102711687-102711737	AG04450	lung:	fetal
38	chr7:102711687-102711737	NHBE	bronchial:	n/a
39	chr7:102711687-102711737	SK-N-MC	brain:	n/a
40	chr7:102711687-102711737	CMK	blood:	n/a
41	chr7:102711687-102711737	HEK293	kidney:	embryo
42	chr7:102711687-102711737	HCM	heart:	n/a
43	chr7:102711687-102711737	K562	blood:	n/a
44	chr7:102711687-102711737	HRCEpiC	kidney:	n/a
45	chr7:102711687-102711737	NH-A	brain:	n/a
46	chr7:102711687-102711737	HepG2	liver:	n/a
47	chr7:102711687-102711737	MCF-7	breast:	n/a
48	chr7:102711687-102711737	GM06990	blood:	n/a
49	chr7:102711687-102711737	NHDF-neo	bronchial:	n/a
50	chr7:102711687-102711737	HRPEpiC	eye:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:102676967..102679361-chr7:102702578..102705004,2	K562	blood:
2	chr7:102712172..102716042-chr7:102726342..102729326,4	K562	blood:
3	chr7:102708220..102712161-chr7:102714525..102717019,5	K562	blood:
4	chr7:102691392..102694110-chr7:102703544..102706469,2	K562	blood:
5	chr7:102620399..102622083-chr7:102705547..102707771,2	K562	blood:
6	chr7:102710661..102713218-chr7:102714768..102717114,2	K562	blood:
7	chr7:102704633..102706824-chr7:102709048..102710835,2	MCF-7	breast:
8	chr7:102668956..102671176-chr7:102710132..102712664,2	K562	blood:
9	chr7:102706745..102709062-chr7:102713643..102715718,3	MCF-7	breast:
10	chr7:102711380..102713849-chr7:102713852..102716556,3	MCF-7	breast:
11	chr7:102389656..102391894-chr7:102702213..102705034,2	MCF-7	breast:
12	chr7:102700472..102704073-chr7:102705229..102707917,4	K562	blood:
13	chr7:102704633..102706824-chr7:102709048..102710835,2	MCF-7	breast:
14	chr7:102704923..102706991-chr7:102714522..102716456,2	MCF-7	breast:
15	chr7:102705659..102708585-chr7:102755906..102758111,2	K562	blood:
16	chr7:102701175..102706120-chr7:102711307..102716730,7	K562	blood:
17	chr7:102704001..102706200-chr7:102714762..102716967,2	K562	blood:

No data

Variant related genes	Relation type
ARMC10	TF binding region
ARMC10	CpG island
ENSG00000161040	chromatin interactions
ENSG00000222011	chromatin interactions
ENSG00000170632	chromatin interactions
ENSG00000236226	chromatin interactions

Extended variants
information (count: 276 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:276 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550268817	chr7:102704814-102704815	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs62482902	chr7:102704835-102704836	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs79642215	chr7:102704879-102704880	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs78675314	chr7:102704887-102704888	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs541402716	chr7:102704916-102704917	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs559517372	chr7:102704923-102704924	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs376223504	chr7:102704931-102704932	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs138539152	chr7:102704938-102704939	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs576593563	chr7:102705066-102705067	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs543626659	chr7:102705101-102705102	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs558647727	chr7:102705130-102705131	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs189407919	chr7:102705346-102705347	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs369405191	chr7:102705349-102705350	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs372786884	chr7:102705396-102705397	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs79849960	chr7:102705432-102705433	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs192164000	chr7:102705473-102705474	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs529598038	chr7:102705503-102705504	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs28452903	chr7:102705555-102705556	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs200791261	chr7:102705618-102705619	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs35067621	chr7:102705619-102705620	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs533676398	chr7:102705700-102705701	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs184423197	chr7:102705728-102705729	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs147328886	chr7:102705763-102705764	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs189522352	chr7:102705781-102705782	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs373631942	chr7:102705816-102705817	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs181884333	chr7:102705832-102705833	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs545335076	chr7:102705865-102705866	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs540116903	chr7:102705868-102705869	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs148342745	chr7:102705869-102705870	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs532497110	chr7:102705894-102705895	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs547864301	chr7:102705968-102705969	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs186070074	chr7:102705969-102705970	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs141534540	chr7:102705970-102705971	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs536615886	chr7:102706168-102706169	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs34669834	chr7:102706202-102706203	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs189445430	chr7:102706205-102706206	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs181433965	chr7:102706214-102706215	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs537686089	chr7:102706296-102706297	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs558878411	chr7:102706311-102706312	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs150531333	chr7:102706317-102706318	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs115717864	chr7:102706347-102706348	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs531012651	chr7:102706368-102706369	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs552612181	chr7:102706370-102706371	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs574114614	chr7:102706401-102706402	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs548638906	chr7:102706458-102706459	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs139536447	chr7:102706550-102706551	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs186607853	chr7:102706557-102706558	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs575439874	chr7:102706574-102706575	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs78172596	chr7:102706599-102706600	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs569869438	chr7:102706609-102706610	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102679200-102713800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr7:102684200-102708000	Weak transcription	Pancreas	Pancrea
3	chr7:102692800-102712800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr7:102702200-102713800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr7:102702200-102714600	Weak transcription	Ovary	ovary
6	chr7:102706000-102706200	Weak transcription	K562	blood
7	chr7:102706200-102706800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr7:102706400-102706600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr7:102706400-102706800	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr7:102706800-102714000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr7:102708000-102708200	ZNF genes & repeats	Pancreas	Pancrea
12	chr7:102708200-102709200	Weak transcription	Pancreas	Pancrea
13	chr7:102708400-102709400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:102708600-102709000	Enhancers	Fetal Lung	lung
15	chr7:102709000-102714200	Weak transcription	Fetal Lung	lung
16	chr7:102709200-102710200	Enhancers	Pancreas	Pancrea
17	chr7:102709400-102710000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
18	chr7:102710200-102711400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr7:102710200-102713800	Weak transcription	Pancreas	Pancrea
20	chr7:102710200-102714400	Weak transcription	Brain Angular Gyrus	brain
21	chr7:102711200-102711400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr7:102711200-102711400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr7:102711400-102714000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr7:102711400-102714400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr7:102712800-102713000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr7:102712800-102713000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr7:102712800-102713000	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr7:102712800-102713000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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