Variant report

Variant	esv3438638
Chromosome Location	chr7:150814869-150817367
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:21)
CpG islands
(count:366)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:21 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr7:150816620-150816770	GM12872	blood:	n/a	chr7:150816726-150816734 chr7:150816725-150816733 chr7:150816637-150816650
2	EGR1	chr7:150817026-150817349	K562	blood:	n/a	chr7:150817252-150817262 chr7:150817310-150817323 chr7:150817247-150817260
3	HMGN3	chr7:150816881-150816886	K562	blood:	n/a	n/a
4	POLR2A	chr7:150815620-150815771	K562	blood:	n/a	n/a
5	POLR2A	chr7:150814548-150814976	K562	blood:	n/a	n/a
6	POLR2A	chr7:150817235-150817248	Hela-S3	cervix:	n/a	n/a
7	POLR2A	chr7:150816760-150817450	K562	blood:	n/a	n/a
8	POLR2A	chr7:150815125-150815185	K562	blood:	n/a	n/a
9	POLR2A	chr7:150817124-150817181	K562	blood:	n/a	n/a
10	POLR2A	chr7:150817020-150817174	K562	blood:	n/a	n/a
11	POLR2A	chr7:150815523-150815611	K562	blood:	n/a	n/a
12	POLR2A	chr7:150815902-150816180	K562	blood:	n/a	n/a
13	POLR2A	chr7:150816525-150816800	K562	blood:	n/a	n/a
14	POLR2A	chr7:150815337-150815418	Hela-S3	cervix:	n/a	n/a
15	POLR2A	chr7:150815229-150815795	K562	blood:	n/a	n/a
16	POLR2A	chr7:150815930-150816178	K562	blood:	n/a	n/a
17	POLR2A	chr7:150816501-150816517	K562	blood:	n/a	n/a
18	POLR2A	chr7:150815228-150815428	K562	blood:	n/a	n/a
19	POLR2A	chr7:150817053-150817068	K562	blood:	n/a	n/a
20	ZKSCAN1	chr7:150815420-150815425	Hela-S3	cervix:	n/a	n/a
21	ZNF263	chr7:150817191-150817346	HEK293-T-REx	kidney:	n/a	chr7:150817245-150817254

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150817197-150817247	AG09309	skin:	n/a
2	chr7:150815445-150815495	LNCaP	prostate:	n/a
3	chr7:150815445-150815495	HCM	heart:	n/a
4	chr7:150815445-150815495	ECC-1	luminal epithelium:	n/a
5	chr7:150816834-150816884	H1-hESC	embryonic stem cell:	embryo
6	chr7:150817013-150817063	GM12891	blood:	n/a
7	chr7:150817013-150817063	A549	lung:	n/a
8	chr7:150815391-150815441	NHDF-neo	bronchial:	n/a
9	chr7:150815320-150815370	BJ	skin:	n/a
10	chr7:150817013-150817063	HEEpiC	esophagus:	n/a
11	chr7:150817197-150817247	SK-N-MC	brain:	n/a
12	chr7:150817197-150817247	LNCaP	prostate:	n/a
13	chr7:150817013-150817063	Caco-2	colon:	n/a
14	chr7:150817197-150817247	BE2_C	brain:	n/a
15	chr7:150816834-150816884	NB4	blood:	n/a
16	chr7:150816834-150816884	SK-N-SH_RA	brain:	n/a
17	chr7:150817013-150817063	MCF-7	breast:	n/a
18	chr7:150817197-150817247	SK-N-SH	brain:	n/a
19	chr7:150815320-150815370	SKMC	muscle:	n/a
20	chr7:150816834-150816884	MCF-7	breast:	n/a
21	chr7:150815391-150815441	AG10803	skin:	n/a
22	chr7:150815391-150815441	AG09319	gingival:	n/a
23	chr7:150815445-150815495	AoSMC	blood vessel:	n/a
24	chr7:150816834-150816884	HCM	heart:	n/a
25	chr7:150815445-150815495	Hela-S3	cervix:	n/a
26	chr7:150817197-150817247	HEK293	kidney:	embryo
27	chr7:150817197-150817247	AG10803	skin:	n/a
28	chr7:150815445-150815495	SAEC	small airway:	n/a
29	chr7:150817197-150817247	Hela-S3	cervix:	n/a
30	chr7:150815391-150815441	A549	lung:	n/a
31	chr7:150815391-150815441	GM12878	blood:	n/a
32	chr7:150815320-150815370	PFSK-1	brain:	n/a
33	chr7:150817197-150817247	Caco-2	colon:	n/a
34	chr7:150815320-150815370	SK-N-SH_RA	brain:	n/a
35	chr7:150816834-150816884	AG04450	lung:	fetal
36	chr7:150816834-150816884	SKMC	muscle:	n/a
37	chr7:150816834-150816884	SK-N-MC	brain:	n/a
38	chr7:150815391-150815441	Hepatocyte	liver:	n/a
39	chr7:150817197-150817247	PrEC	prostate:	n/a
40	chr7:150816834-150816884	PANC-1	pancreas:	n/a
41	chr7:150817013-150817063	NH-A	brain:	n/a
42	chr7:150816834-150816884	NT2-D1	testis:	n/a
43	chr7:150817197-150817247	PFSK-1	brain:	n/a
44	chr7:150817013-150817063	HIPEpiC	eye:	n/a
45	chr7:150817013-150817063	AoSMC	blood vessel:	n/a
46	chr7:150815391-150815441	AG09309	skin:	n/a
47	chr7:150817013-150817063	GM12878	blood:	n/a
48	chr7:150815445-150815495	NT2-D1	testis:	n/a
49	chr7:150817013-150817063	SKMC	muscle:	n/a
50	chr7:150816834-150816884	HEK293	kidney:	embryo

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:8094111..8096395-chr7:150814186..150816873,2	MCF-7	breast:
2	chr7:150805011..150810412-chr7:150810806..150815520,8	K562	blood:
3	chr7:150817042..150818782-chr7:150819382..150821039,2	MCF-7	breast:
4	chr7:150813337..150816221-chr7:150868567..150872033,3	K562	blood:
5	chr7:150807803..150810009-chr7:150811928..150814974,4	MCF-7	breast:
6	chr7:150817194..150819802-chr7:150827702..150830037,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC4A2-2	chr7:150817074-150817232	NONHSAT124193
2	lnc-SLC4A2-2	chr7:150816284-150816341	NONHSAT124193

No data

Variant related genes	Relation type
AGAP3	TF binding region
AGAP3	CpG island
ENSG00000243350	chromatin interactions
ENSG00000107485	chromatin interactions
ENSG00000133612	chromatin interactions
ENSG00000197308	chromatin interactions
ENSG00000164900	chromatin interactions

Extended variants
information (count: 139 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:139 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199728267	chr7:150814904-150814905	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs527671411	chr7:150814909-150814910	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs547854097	chr7:150814910-150814911	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs371121820	chr7:150814913-150814914	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs142633074	chr7:150815004-150815005	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs565143069	chr7:150815013-150815014	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs549963906	chr7:150815014-150815015	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs35845741	chr7:150815024-150815025	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs6945773	chr7:150815039-150815040	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs113041890	chr7:150815041-150815042	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs79006664	chr7:150815062-150815063	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs150974291	chr7:150815086-150815087	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs142296673	chr7:150815140-150815141	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs534311492	chr7:150815151-150815152	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs147773658	chr7:150815167-150815168	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs180977569	chr7:150815168-150815169	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs141168359	chr7:150815260-150815261	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs367827938	chr7:150815269-150815270	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs183681331	chr7:150815276-150815277	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs146925587	chr7:150815277-150815278	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs542435338	chr7:150815278-150815279	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs374773519	chr7:150815313-150815314	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs562236426	chr7:150815322-150815323	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs200603291	chr7:150815326-150815327	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs368289264	chr7:150815331-150815332	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs372502191	chr7:150815335-150815336	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs73476760	chr7:150815346-150815347	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs541391426	chr7:150815367-150815368	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs369836012	chr7:150815400-150815401	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs372947093	chr7:150815438-150815439	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs548016086	chr7:150815446-150815447	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs376525541	chr7:150815447-150815448	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs369175300	chr7:150815467-150815468	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs550322041	chr7:150815468-150815469	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs144966916	chr7:150815475-150815476	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs567662088	chr7:150815500-150815501	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs549198860	chr7:150815519-150815520	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs537910175	chr7:150815522-150815523	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs189375641	chr7:150815529-150815530	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs534604967	chr7:150815533-150815534	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs199772282	chr7:150815553-150815554	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs376200094	chr7:150815570-150815571	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs61740089	chr7:150815630-150815631	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs62489621	chr7:150815668-150815669	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs373083934	chr7:150815678-150815679	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs569191956	chr7:150815680-150815681	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs372837701	chr7:150815686-150815687	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs371001392	chr7:150815690-150815691	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs200887887	chr7:150815696-150815697	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs201733562	chr7:150815701-150815702	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
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
Wilms tumour	21544195	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
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:200 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150789000-150815400	Weak transcription	GM12878-XiMat	blood
2	chr7:150802600-150821400	Weak transcription	Hela-S3	cervix
3	chr7:150808200-150815200	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr7:150808600-150815000	Weak transcription	Brain Substantia Nigra	brain
5	chr7:150811200-150816200	Weak transcription	NHDF-Ad	bronchial
6	chr7:150811600-150815200	Weak transcription	Rectal Smooth Muscle	rectum
7	chr7:150811600-150815400	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr7:150811600-150821200	Weak transcription	Fetal Kidney	kidney
9	chr7:150812400-150829600	Weak transcription	Small Intestine	intestine
10	chr7:150812600-150839800	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr7:150812800-150815200	Weak transcription	Ovary	ovary
12	chr7:150812800-150815200	Weak transcription	Osteobl	bone
13	chr7:150812800-150815400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
14	chr7:150812800-150815600	Weak transcription	Aorta	Aorta
15	chr7:150812800-150815800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr7:150812800-150816200	Flanking Active TSS	Dnd41	blood
17	chr7:150812800-150822400	Weak transcription	Psoas Muscle	Psoas
18	chr7:150813000-150815000	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr7:150813000-150818800	Strong transcription	HepG2	liver
20	chr7:150813000-150821400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr7:150813000-150822400	Strong transcription	NHLF	lung
22	chr7:150813000-150840400	Weak transcription	Primary hematopoietic stem cells	blood
23	chr7:150813000-150843800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr7:150813200-150815000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr7:150813200-150815000	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr7:150813200-150815200	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr7:150813200-150815200	Weak transcription	Left Ventricle	heart
28	chr7:150813200-150815400	Weak transcription	HSMMtube	muscle
29	chr7:150813200-150815600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr7:150813200-150815600	Weak transcription	Brain Hippocampus Middle	brain
31	chr7:150813200-150815800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr7:150813200-150816200	Weak transcription	HUVEC	blood vessel
33	chr7:150813200-150821000	Weak transcription	Fetal Brain Male	brain
34	chr7:150813200-150822200	Weak transcription	Right Atrium	heart
35	chr7:150813400-150815000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr7:150813400-150815200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr7:150813400-150815400	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr7:150813400-150816000	Genic enhancers	Spleen	Spleen
39	chr7:150813400-150822800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr7:150813600-150815000	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr7:150813600-150815200	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr7:150813600-150815200	Weak transcription	Colon Smooth Muscle	Colon
43	chr7:150813600-150815200	Transcr. at gene 5' and 3'	NHEK	skin
44	chr7:150813600-150815600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr7:150813600-150816000	Weak transcription	HSMM	muscle
46	chr7:150813600-150819200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr7:150813600-150821200	Strong transcription	Fetal Stomach	stomach
48	chr7:150813600-150821400	Strong transcription	Right Ventricle	heart
49	chr7:150813600-150822200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr7:150813600-150822400	Strong transcription	Fetal Brain Female	brain

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