Variant report

Variant	rs73337354
Chromosome Location	chr7:7291561-7291562
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RCOR1	chr7:7291342-7291880	GM12878	blood:	n/a	n/a
2	BHLHE40	chr7:7291377-7291775	GM12878	blood:	n/a	n/a
3	SPI1	chr7:7291095-7292136	GM12878	blood:	n/a	chr7:7291563-7291576 chr7:7291566-7291575 chr7:7291570-7291579 chr7:7291657-7291666 chr7:7291564-7291577
4	TCF12	chr7:7291409-7291679	GM12878	blood:	n/a	n/a
5	SPI1	chr7:7291431-7291797	HL-60	blood:	n/a	chr7:7291563-7291576 chr7:7291566-7291575 chr7:7291570-7291579 chr7:7291657-7291666 chr7:7291564-7291577
6	SPI1	chr7:7291257-7291883	HL-60	blood:	n/a	chr7:7291563-7291576 chr7:7291566-7291575 chr7:7291570-7291579 chr7:7291657-7291666 chr7:7291564-7291577
7	ATF2	chr7:7291267-7291858	GM12878	blood:	n/a	n/a
8	POLR2A	chr7:7291100-7291947	HepG2	liver:	n/a	n/a
9	EBF1	chr7:7291366-7291705	GM12878	blood:	n/a	n/a
10	RUNX3	chr7:7291343-7291685	GM12878	blood:	n/a	n/a
11	SPI1	chr7:7291228-7291812	GM12891	blood:	n/a	chr7:7291563-7291576 chr7:7291566-7291575 chr7:7291570-7291579 chr7:7291657-7291666 chr7:7291564-7291577
12	CHD2	chr7:7291392-7291774	GM12878	blood:	n/a	n/a
13	POU2F2	chr7:7291468-7291698	GM12891	blood:	n/a	chr7:7291660-7291670
14	SPI1	chr7:7291312-7291792	GM12891	blood:	n/a	chr7:7291563-7291576 chr7:7291566-7291575 chr7:7291570-7291579 chr7:7291657-7291666 chr7:7291564-7291577
15	TCF12	chr7:7291412-7291667	GM12878	blood:	n/a	n/a
16	BCL11A	chr7:7291339-7291760	GM12878	blood:	n/a	chr7:7291570-7291579 chr7:7291657-7291666
17	STAT1	chr7:7291392-7291699	GM12878	blood:	n/a	chr7:7291570-7291581
18	EBF1	chr7:7291318-7291724	GM12878	blood:	n/a	n/a
19	TCF3	chr7:7291450-7291719	GM12878	blood:	n/a	n/a
20	PAX5	chr7:7291399-7291633	GM12891	blood:	n/a	chr7:7291570-7291579
21	BATF	chr7:7291379-7291691	GM12878	blood:	n/a	n/a
22	NFIC	chr7:7291248-7291881	GM12878	blood:	n/a	n/a
23	YY1	chr7:7291456-7291812	GM12892	blood:	n/a	n/a
24	FOXM1	chr7:7291283-7291793	GM12878	blood:	n/a	n/a
25	EP300	chr7:7291383-7291775	GM12878	blood:	n/a	chr7:7291565-7291579
26	NFIC	chr7:7291297-7291938	GM12878	blood:	n/a	n/a
27	RUNX3	chr7:7291272-7291777	GM12878	blood:	n/a	n/a
28	PAX5	chr7:7291356-7291801	GM12878	blood:	n/a	chr7:7291570-7291579
29	ELK1	chr7:7291496-7291812	GM12878	blood:	n/a	n/a
30	IRF4	chr7:7291321-7291841	GM12878	blood:	n/a	n/a
31	REST	chr7:7291421-7291687	Hela-S3	cervix:	n/a	n/a
32	WRNIP1	chr7:7291471-7291671	GM12878	blood:	n/a	n/a
33	MXI1	chr7:7291435-7291874	GM12878	blood:	n/a	n/a
34	SPI1	chr7:7291303-7291748	GM12878	blood:	n/a	chr7:7291563-7291576 chr7:7291566-7291575 chr7:7291570-7291579 chr7:7291657-7291666 chr7:7291564-7291577
35	BCLAF1	chr7:7291262-7291865	GM12878	blood:	n/a	chr7:7291570-7291579 chr7:7291657-7291666
36	ZNF143	chr7:7291417-7291754	GM12878	blood:	n/a	n/a
37	SPI1	chr7:7291400-7291726	GM12878	blood:	n/a	chr7:7291563-7291576 chr7:7291566-7291575 chr7:7291570-7291579 chr7:7291657-7291666 chr7:7291564-7291577
38	IRF4	chr7:7291334-7291813	GM12878	blood:	n/a	n/a
39	SPI1	chr7:7291464-7291619	K562	blood:	n/a	chr7:7291563-7291576 chr7:7291566-7291575 chr7:7291570-7291579 chr7:7291564-7291577
40	EP300	chr7:7291389-7291914	GM12878	blood:	n/a	chr7:7291565-7291579
41	BCLAF1	chr7:7291366-7291778	GM12878	blood:	n/a	chr7:7291570-7291579 chr7:7291657-7291666
42	EP300	chr7:7291330-7291800	GM12878	blood:	n/a	chr7:7291565-7291579
43	TCF3	chr7:7291337-7291784	GM12878	blood:	n/a	n/a
44	BCL11A	chr7:7291400-7291703	GM12878	blood:	n/a	chr7:7291570-7291579 chr7:7291657-7291666
45	MAX	chr7:7291396-7291739	NB4	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:7291514-7291564	HCPEpiC	choroid plexus:	n/a
2	chr7:7291514-7291564	HUVEC	blood vessel:	n/a
3	chr7:7291514-7291564	AG10803	skin:	n/a
4	chr7:7291514-7291564	PFSK-1	brain:	n/a
5	chr7:7291514-7291564	U87	brain:	n/a
6	chr7:7291514-7291564	ECC-1	luminal epithelium:	n/a
7	chr7:7291514-7291564	HCF	heart:	n/a
8	chr7:7291514-7291564	HRCEpiC	kidney:	n/a
9	chr7:7291514-7291564	GM19239	blood:	n/a
10	chr7:7291514-7291564	HRPEpiC	eye:	n/a
11	chr7:7291514-7291564	PANC-1	pancreas:	n/a
12	chr7:7291514-7291564	GM12891	blood:	n/a
13	chr7:7291514-7291564	RPTEC	kidney:	n/a
14	chr7:7291514-7291564	NT2-D1	testis:	n/a
15	chr7:7291514-7291564	MCF10A-Er-Src	breast:	n/a
16	chr7:7291514-7291564	SK-N-SH_RA	brain:	n/a
17	chr7:7291514-7291564	BJ	skin:	n/a
18	chr7:7291514-7291564	AG09319	gingival:	n/a
19	chr7:7291514-7291564	AG04449	skin:	fetal
20	chr7:7291514-7291564	SK-N-SH	brain:	n/a
21	chr7:7291514-7291564	BE2_C	brain:	n/a
22	chr7:7291514-7291564	GM12892	blood:	n/a
23	chr7:7291514-7291564	ovcar-3	ovarian:	n/a
24	chr7:7291514-7291564	AoSMC	blood vessel:	n/a
25	chr7:7291514-7291564	AG09309	skin:	n/a
26	chr7:7291514-7291564	NB4	blood:	n/a
27	chr7:7291514-7291564	HL-60	blood:	n/a
28	chr7:7291514-7291564	GM12878	blood:	n/a
29	chr7:7291514-7291564	MCF-7	breast:	n/a
30	chr7:7291514-7291564	HIPEpiC	eye:	n/a
31	chr7:7291514-7291564	Hela-S3	cervix:	n/a
32	chr7:7291514-7291564	H1-hESC	embryonic stem cell:	embryo
33	chr7:7291514-7291564	K562	blood:	n/a
34	chr7:7291514-7291564	NHBE	bronchial:	n/a
35	chr7:7291514-7291564	SKMC	muscle:	n/a
36	chr7:7291514-7291564	HNPCEpiC	eye:	n/a
37	chr7:7291514-7291564	HAEpiC	amniotic membrane:	n/a
38	chr7:7291514-7291564	Hepatocyte	liver:	n/a
39	chr7:7291514-7291564	SK-N-MC	brain:	n/a
40	chr7:7291514-7291564	NH-A	brain:	n/a
41	chr7:7291514-7291564	HCT-116	colon:	n/a
42	chr7:7291514-7291564	CMK	blood:	n/a
43	chr7:7291514-7291564	HEK293	kidney:	embryo
44	chr7:7291514-7291564	IMR90	lung:	fetal
45	chr7:7291514-7291564	PrEC	prostate:	n/a
46	chr7:7291514-7291564	Caco-2	colon:	n/a
47	chr7:7291514-7291564	SAEC	small airway:	n/a
48	chr7:7291514-7291564	HMEC	breast:	n/a
49	chr7:7291514-7291564	T-47D	breast:	n/a
50	chr7:7291514-7291564	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:7247420..7249053-chr7:7289694..7292238,2	K562	blood:

Variant related genes	Relation type
ENSG00000230825	TF binding region
ENSG00000230825	CpG island

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10235948	1.00[AMR][1000 genomes]
rs10235971	1.00[AMR][1000 genomes]
rs10246129	1.00[AMR][1000 genomes]
rs10256653	1.00[AMR][1000 genomes]
rs10259685	1.00[AMR][1000 genomes]
rs10260294	1.00[AMR][1000 genomes]
rs10260960	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10260962	1.00[AMR][1000 genomes]
rs10269694	1.00[AMR][1000 genomes]
rs10513	1.00[AMR][1000 genomes]
rs17166290	1.00[AMR][1000 genomes]
rs28539228	1.00[AMR][1000 genomes]
rs28635667	1.00[AMR][1000 genomes]
rs73337332	1.00[AMR][1000 genomes]
rs73337353	1.00[AMR][1000 genomes]
rs73337376	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73337383	1.00[AMR][1000 genomes]
rs73337386	1.00[AMR][1000 genomes]
rs73676814	1.00[AMR][1000 genomes]
rs9655509	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015277	chr7:6705439-7303195	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv1023133	chr7:6854098-7516700	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
3	nsv869091	chr7:6927461-7567820	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
4	nsv949293	chr7:6990891-7711883	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
5	nsv464300	chr7:7040176-7368699	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
6	nsv606033	chr7:7040176-7368699	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
7	nsv1016369	chr7:7053923-7375567	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
8	nsv1023788	chr7:7053923-7407783	Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
9	nsv538720	chr7:7053923-7407783	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
10	nsv1032813	chr7:7053923-7497484	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
11	nsv1030246	chr7:7053923-7569633	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
12	nsv1019498	chr7:7053923-7668373	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
13	nsv538721	chr7:7053923-7668373	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
14	nsv1032974	chr7:7145831-7393218	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
15	nsv1026758	chr7:7187491-8075259	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
16	esv2758102	chr7:7209911-7493901	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
17	esv2759505	chr7:7209911-7493901	Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Weak transcription Genic 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 miRNA target site	33 gene(s)	inside rSNPs	diseases
18	nsv464301	chr7:7252775-7442169	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
19	nsv606035	chr7:7252775-7442169	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
20	nsv469770	chr7:7261414-7453821	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
21	nsv433018	chr7:7269171-7348778	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
22	nsv606036	chr7:7273559-7343909	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
23	esv2756798	chr7:7280062-7441775	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
24	nsv8042	chr7:7291138-7328841	Flanking Active TSS Active TSS Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
25	esv3475554	chr7:7291482-7325374	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
26	esv3475552	chr7:7291507-7325362	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
27	esv3475555	chr7:7291507-7325362	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7250800-7296600	Weak transcription	Spleen	Spleen
2	chr7:7256800-7297000	Weak transcription	Lung	lung
3	chr7:7257600-7298200	Weak transcription	Ovary	ovary
4	chr7:7257600-7299800	Weak transcription	Fetal Stomach	stomach
5	chr7:7260400-7297200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr7:7261600-7296800	Weak transcription	Aorta	Aorta
7	chr7:7261600-7298000	Weak transcription	Pancreas	Pancrea
8	chr7:7261600-7299400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr7:7271400-7298200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr7:7272400-7295000	Weak transcription	Small Intestine	intestine
11	chr7:7272400-7296600	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr7:7273400-7311200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr7:7274600-7301600	Weak transcription	Brain Germinal Matrix	brain
14	chr7:7275600-7298200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr7:7275600-7305400	Weak transcription	Gastric	stomach
16	chr7:7276200-7298600	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr7:7276800-7304000	Weak transcription	Fetal Brain Male	brain
18	chr7:7277200-7292800	Weak transcription	NHEK	skin
19	chr7:7277200-7306200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr7:7277600-7296600	Weak transcription	Psoas Muscle	Psoas
21	chr7:7277600-7297800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr7:7277800-7294600	Weak transcription	Fetal Heart	heart
23	chr7:7278400-7299600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr7:7279000-7296600	Weak transcription	Brain Hippocampus Middle	brain
25	chr7:7279000-7296800	Weak transcription	Fetal Muscle Leg	muscle
26	chr7:7279200-7298600	Weak transcription	Thymus	Thymus
27	chr7:7279200-7309800	Weak transcription	Brain Anterior Caudate	brain
28	chr7:7279800-7296400	Weak transcription	HMEC	breast
29	chr7:7279800-7300000	Weak transcription	Fetal Brain Female	brain
30	chr7:7279800-7301000	Weak transcription	A549	lung
31	chr7:7279800-7304600	Weak transcription	NHDF-Ad	bronchial
32	chr7:7280000-7294400	Weak transcription	Fetal Intestine Large	intestine
33	chr7:7280000-7296800	Weak transcription	Left Ventricle	heart
34	chr7:7280000-7298000	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr7:7280000-7299800	Weak transcription	Placenta	Placenta
36	chr7:7280000-7300200	Weak transcription	NH-A	brain
37	chr7:7280000-7300400	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr7:7280000-7302800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr7:7283400-7299800	Weak transcription	K562	blood
40	chr7:7283800-7300000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr7:7284200-7298600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr7:7284400-7299600	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr7:7285000-7296600	Weak transcription	Primary T cells fromperipheralblood	blood
44	chr7:7285000-7300400	Weak transcription	Esophagus	oesophagus
45	chr7:7285000-7310600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr7:7285400-7302800	Weak transcription	HSMMtube	muscle
47	chr7:7286000-7291600	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr7:7286000-7292200	Weak transcription	Osteobl	bone
49	chr7:7286200-7296600	Weak transcription	Fetal Thymus	thymus
50	chr7:7286200-7298000	Weak transcription	H9 Cell Line	embryonic stem cell

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