Variant report

Variant	rs13230247
Chromosome Location	chr7:6680235-6680236
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:48)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:48 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	IRF1	chr7:6679907-6680411	K562	blood:	n/a	n/a
2	CEBPB	chr7:6679892-6680277	K562	blood:	n/a	n/a
3	POLR2A	chr7:6679659-6680395	K562	blood:	n/a	n/a
4	TEAD4	chr7:6679825-6680295	K562	blood:	n/a	n/a
5	MAZ	chr7:6679840-6680411	K562	blood:	n/a	n/a
6	TEAD4	chr7:6679845-6680273	K562	blood:	n/a	n/a
7	TBL1XR1	chr7:6679849-6680279	K562	blood:	n/a	n/a
8	POLR2A	chr7:6679798-6680239	K562	blood:	n/a	n/a
9	MAX	chr7:6679777-6680266	NB4	blood:	n/a	chr7:6680036-6680046
10	EGR1	chr7:6679842-6680300	K562	blood:	n/a	n/a
11	ZNF143	chr7:6680232-6680295	H1-hESC	embryonic stem cell:	n/a	n/a
12	YY1	chr7:6679758-6680238	K562	blood:	n/a	n/a
13	NR2F2	chr7:6679910-6680255	K562	blood:	n/a	n/a
14	POLR2A	chr7:6679104-6684327	K562	blood:	n/a	n/a
15	ZBTB7A	chr7:6680125-6680419	K562	blood:	n/a	n/a
16	EGR1	chr7:6679817-6680343	K562	blood:	n/a	n/a
17	POLR2A	chr7:6679710-6680698	K562	blood:	n/a	n/a
18	HMGN3	chr7:6680013-6680306	K562	blood:	n/a	n/a
19	MYC	chr7:6679836-6680303	K562	blood:	n/a	chr7:6680036-6680046
20	RCOR1	chr7:6679882-6680441	K562	blood:	n/a	n/a
21	NR2F2	chr7:6679751-6680441	K562	blood:	n/a	n/a
22	ELF1	chr7:6679810-6680300	K562	blood:	n/a	n/a
23	POLR2A	chr7:6679933-6680420	K562	blood:	n/a	n/a
24	TBP	chr7:6679885-6680263	K562	blood:	n/a	n/a
25	TBL1XR1	chr7:6680127-6680235	K562	blood:	n/a	n/a
26	TRIM28	chr7:6679682-6680365	K562	blood:	n/a	n/a
27	CEBPB	chr7:6679964-6680434	K562	blood:	n/a	n/a
28	CBX3	chr7:6679531-6680589	K562	blood:	n/a	n/a
29	KAP1	chr7:6679800-6680668	HEK293	kidney:	n/a	n/a
30	CHD2	chr7:6680088-6680425	H1-hESC	embryonic stem cell:	n/a	n/a
31	BHLHE40	chr7:6679828-6680319	K562	blood:	n/a	n/a
32	CHD2	chr7:6679927-6680429	K562	blood:	n/a	n/a
33	MYC	chr7:6679851-6680339	K562	blood:	n/a	chr7:6680036-6680046
34	STAT5A	chr7:6679852-6680300	K562	blood:	n/a	n/a
35	JUND	chr7:6679885-6680475	K562	blood:	n/a	n/a
36	MYC	chr7:6679677-6680278	NB4	blood:	n/a	chr7:6680036-6680046
37	USF1	chr7:6679746-6680262	K562	blood:	n/a	n/a
38	MAX	chr7:6679657-6680433	K562	blood:	n/a	chr7:6680036-6680046 chr7:6679667-6679686
39	EP300	chr7:6679894-6680251	K562	blood:	n/a	n/a
40	POLR2A	chr7:6680072-6680409	GM12878	blood:	n/a	n/a
41	SIN3A	chr7:6680048-6680344	H1-hESC	embryonic stem cell:	n/a	n/a
42	PBX3	chr7:6680037-6680236	GM12878	blood:	n/a	n/a
43	TAL1	chr7:6679978-6680270	K562	blood:	n/a	n/a
44	FOSL1	chr7:6679906-6680236	K562	blood:	n/a	n/a
45	UBTF	chr7:6680007-6680376	K562	blood:	n/a	n/a
46	MXI1	chr7:6680162-6680380	H1-hESC	embryonic stem cell:	n/a	n/a
47	MAX	chr7:6679833-6680331	K562	blood:	n/a	chr7:6680036-6680046
48	MXI1	chr7:6679906-6680457	K562	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr7:6627001..6634994-chr7:6673643..6681623,15	MCF-7	breast:
2	chr7:6668305..6670110-chr7:6679585..6681865,2	MCF-7	breast:
3	chr7:6674043..6676883-chr7:6677067..6680291,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF853-2	chr7:6679361-6680635	ucscGeneNc_uc003sqr_1

No data

Variant related genes	Relation type
ZNF316	TF binding region
ENSG00000146576	Chromatin interaction
ENSG00000232581	Chromatin interaction

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs13227497	1.00[ASN][1000 genomes]
rs13228621	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13229146	1.00[ASN][1000 genomes]
rs13234726	0.90[ASN][1000 genomes]
rs13237018	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34751372	1.00[ASN][1000 genomes]
rs35051105	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs35692911	0.90[ASN][1000 genomes]
rs940868	0.80[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:39 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034060	chr7:5814823-6745710	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	138 gene(s)	inside rSNPs	diseases
2	nsv538711	chr7:5814823-6745710	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	138 gene(s)	inside rSNPs	diseases
3	nsv949531	chr7:5949371-6753694	Strong transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	129 gene(s)	inside rSNPs	diseases
4	nsv1020236	chr7:6248930-6690377	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
5	nsv830895	chr7:6514781-6722092	Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
6	nsv508444	chr7:6534110-6700527	Bivalent/Poised TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
7	nsv1025220	chr7:6534278-6736802	Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
8	nsv538717	chr7:6534278-6736802	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
9	nsv887431	chr7:6535517-6690240	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
10	nsv515978	chr7:6535517-6698905	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
11	nsv887432	chr7:6535517-6713985	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
12	nsv887434	chr7:6557135-6713985	Strong transcription Active TSS Genic enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
13	nsv606001	chr7:6563109-6683454	Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
14	nsv606002	chr7:6567114-6713985	Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
15	nsv887435	chr7:6613604-6713985	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
16	nsv824002	chr7:6618087-6716961	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
17	nsv824003	chr7:6620920-6721409	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
18	nsv887436	chr7:6626922-6721661	Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
19	esv1797143	chr7:6628177-6705439	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
20	nsv606003	chr7:6628242-6713985	Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
21	nsv606004	chr7:6643664-6692573	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
22	nsv887437	chr7:6645281-6704332	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
23	nsv887438	chr7:6652740-6709600	ZNF genes & repeats Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
24	esv1820840	chr7:6656753-6698297	Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
25	esv1821128	chr7:6656753-6698297	Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
26	esv1824232	chr7:6656753-6706631	Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
27	esv1841674	chr7:6656753-6706631	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
28	nsv464297	chr7:6656897-6698905	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
29	nsv606005	chr7:6656897-6698905	Strong transcription Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
30	nsv606006	chr7:6659509-6721661	ZNF genes & repeats Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
31	nsv606007	chr7:6666501-6692407	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
32	esv1803673	chr7:6671496-6721661	Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
33	esv1834684	chr7:6671496-6721661	Active TSS Strong transcription Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
34	esv1800946	chr7:6673956-6706631	Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
35	esv1813782	chr7:6673956-6706631	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
36	esv1818550	chr7:6673956-6706631	Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
37	esv1826832	chr7:6673956-6706631	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
38	esv1839832	chr7:6673956-6706631	Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
39	esv1851662	chr7:6673956-6706631	Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6678000-6680600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr7:6678000-6691600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr7:6678200-6680400	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr7:6678200-6680400	Weak transcription	NH-A	brain
5	chr7:6678200-6680600	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr7:6678200-6680600	Weak transcription	HSMMtube	muscle
7	chr7:6678200-6681000	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr7:6678200-6681000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr7:6678200-6681000	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr7:6678200-6681200	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr7:6678200-6681600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr7:6678200-6681600	Weak transcription	Fetal Kidney	kidney
13	chr7:6678200-6682400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr7:6678200-6683200	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr7:6678200-6683400	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr7:6678200-6683800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr7:6678200-6684200	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr7:6678200-6685000	Strong transcription	NHEK	skin
19	chr7:6678200-6698200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr7:6678400-6680400	Weak transcription	Ovary	ovary
21	chr7:6678400-6680400	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr7:6678400-6681000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr7:6678400-6681000	Weak transcription	Aorta	Aorta
24	chr7:6678400-6681200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr7:6678400-6683000	Weak transcription	Small Intestine	intestine
26	chr7:6678400-6691600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr7:6678400-6691600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr7:6678600-6680400	Weak transcription	Brain Cingulate Gyrus	brain
29	chr7:6678600-6680600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr7:6678600-6680600	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr7:6678600-6681200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr7:6678600-6681200	Weak transcription	Brain Angular Gyrus	brain
33	chr7:6678600-6681600	Weak transcription	HUVEC	blood vessel
34	chr7:6678600-6682800	Weak transcription	Stomach Mucosa	stomach
35	chr7:6678600-6687800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:6678600-6687800	Strong transcription	Fetal Intestine Large	intestine
37	chr7:6678600-6689600	Strong transcription	Fetal Intestine Small	intestine
38	chr7:6678800-6680400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr7:6678800-6680600	Weak transcription	Brain Anterior Caudate	brain
40	chr7:6678800-6680600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr7:6678800-6680600	Weak transcription	Colon Smooth Muscle	Colon
42	chr7:6678800-6680800	Genic enhancers	Dnd41	blood
43	chr7:6678800-6681400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr7:6678800-6681400	Strong transcription	HSMM	muscle
45	chr7:6678800-6681600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr7:6678800-6682000	Weak transcription	Psoas Muscle	Psoas
47	chr7:6678800-6685600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr7:6678800-6688600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr7:6678800-6689600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr7:6678800-6691200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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