Variant report

Variant	nsv608463
Chromosome Location	chr7:136825522-136882925
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:353)
CpG islands
(count:549)
Chromatin interactive
region (count:13)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:136853987-136854164	HepG2	liver:	n/a	n/a
2	ATF2	chr7:136853857-136854307	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr7:136853848-136854381	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:136880818-136881042	K562	blood:	n/a	n/a
5	BACH1	chr7:136853886-136854162	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:136880793-136881122	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr7:136856791-136856855	GM12878	blood:	n/a	n/a
8	CEBPB	chr7:136835316-136835641	IMR90	lung:	n/a	n/a
9	CEBPB	chr7:136856746-136856949	IMR90	lung:	n/a	chr7:136856865-136856876
10	CEBPB	chr7:136851292-136851308	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr7:136856710-136857042	HepG2	liver:	n/a	chr7:136856865-136856876
12	CEBPB	chr7:136856735-136856935	A549	lung:	n/a	chr7:136856865-136856876
13	CEBPB	chr7:136830658-136831982	IMR90	lung:	n/a	n/a
14	CEBPB	chr7:136851161-136851454	IMR90	lung:	n/a	chr7:136851307-136851316
15	CEBPB	chr7:136853989-136854249	H1-hESC	embryonic stem cell:	n/a	chr7:136854153-136854165
16	CEBPB	chr7:136851211-136851370	K562	blood:	n/a	chr7:136851307-136851316
17	CHD2	chr7:136853979-136854259	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr7:136854020-136854170	Caco-2	colon:	n/a	chr7:136854107-136854128
19	CTCF	chr7:136854040-136854190	HPF	lung:	n/a	chr7:136854107-136854128
20	CTCF	chr7:136854040-136854190	BJ	skin:	n/a	chr7:136854107-136854128
21	CTCF	chr7:136854020-136854170	GM12868	blood:	n/a	chr7:136854107-136854128
22	CTCF	chr7:136853977-136854302	A549	lung:	n/a	chr7:136854107-136854128
23	CTCF	chr7:136854040-136854190	HPAF	blood vessel:	n/a	chr7:136854107-136854128
24	CTCF	chr7:136854040-136854190	HEK293	kidney:	n/a	chr7:136854107-136854128
25	CTCF	chr7:136854020-136854170	A549	lung:	n/a	chr7:136854107-136854128
26	CTCF	chr7:136854080-136854230	GM12864	blood:	n/a	chr7:136854107-136854128
27	CTCF	chr7:136854040-136854190	GM12864	blood:	n/a	chr7:136854107-136854128
28	CTCF	chr7:136854020-136854170	MCF-7	breast:	n/a	chr7:136854107-136854128
29	CTCF	chr7:136854060-136854210	GM12875	blood:	n/a	chr7:136854107-136854128
30	CTCF	chr7:136853978-136854324	HepG2	liver:	n/a	chr7:136854107-136854128
31	CTCF	chr7:136854051-136854190	GM19240	blood:	n/a	chr7:136854107-136854128
32	CTCF	chr7:136859880-136860030	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr7:136854020-136854170	AG04450	lung:	n/a	chr7:136854107-136854128
34	CTCF	chr7:136854040-136854190	Caco-2	colon:	n/a	chr7:136854107-136854128
35	CTCF	chr7:136853980-136854130	Hela-S3	cervix:	n/a	chr7:136854107-136854128
36	CTCF	chr7:136854040-136854190	SAEC	small airway:	n/a	chr7:136854107-136854128
37	CTCF	chr7:136854040-136854190	K562	blood:	n/a	chr7:136854107-136854128
38	CTCF	chr7:136854020-136854170	AG09309	skin:	n/a	chr7:136854107-136854128
39	CTCF	chr7:136853975-136854245	MCF-7	breast:	n/a	chr7:136854107-136854128
40	CTCF	chr7:136854060-136854210	HAc	cerebellar:	n/a	chr7:136854107-136854128
41	CTCF	chr7:136844060-136844210	AG10803	skin:	n/a	n/a
42	CTCF	chr7:136854000-136854150	HCM	heart:	n/a	chr7:136854107-136854128
43	CTCF	chr7:136853998-136854172	GM13977	blood:	n/a	chr7:136854107-136854128
44	CTCF	chr7:136854060-136854210	NHDF-neo	bronchial:	n/a	chr7:136854107-136854128
45	CTCF	chr7:136854040-136854190	HRPEpiC	eye:	n/a	chr7:136854107-136854128
46	CTCF	chr7:136854040-136854190	NHDF-neo	bronchial:	n/a	chr7:136854107-136854128
47	CTCF	chr7:136854024-136854185	Lung_OC	lung:	n/a	chr7:136854107-136854128
48	CTCF	chr7:136854000-136854150	RPTEC	kidney:	n/a	chr7:136854107-136854128
49	CTCF	chr7:136853988-136854227	HUVEC	blood vessel:	n/a	chr7:136854107-136854128
50	CTCF	chr7:136854200-136854350	GM12871	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:136849143-136849193	AoSMC	blood vessel:	n/a
2	chr7:136845265-136845315	GM12892	blood:	n/a
3	chr7:136850736-136850786	HEEpiC	esophagus:	n/a
4	chr7:136849187-136849237	MCF-7	breast:	n/a
5	chr7:136849143-136849193	AG10803	skin:	n/a
6	chr7:136849018-136849068	HCPEpiC	choroid plexus:	n/a
7	chr7:136849317-136849367	NT2-D1	testis:	n/a
8	chr7:136845265-136845315	HAEpiC	amniotic membrane:	n/a
9	chr7:136850736-136850786	HPAEpiC	pulmonary alveolar:	n/a
10	chr7:136849317-136849367	GM12892	blood:	n/a
11	chr7:136849262-136849312	AG10803	skin:	n/a
12	chr7:136849262-136849312	BJ	skin:	n/a
13	chr7:136849143-136849193	GM12878	blood:	n/a
14	chr7:136849143-136849193	HRCEpiC	kidney:	n/a
15	chr7:136845265-136845315	NH-A	brain:	n/a
16	chr7:136849262-136849312	GM06990	blood:	n/a
17	chr7:136845265-136845315	LNCaP	prostate:	n/a
18	chr7:136845265-136845315	ovcar-3	ovarian:	n/a
19	chr7:136849262-136849312	HL-60	blood:	n/a
20	chr7:136879401-136879451	HMEC	breast:	n/a
21	chr7:136832262-136832312	HEEpiC	esophagus:	n/a
22	chr7:136849018-136849068	HEEpiC	esophagus:	n/a
23	chr7:136849018-136849068	MCF-7	breast:	n/a
24	chr7:136849262-136849312	SKMC	muscle:	n/a
25	chr7:136849187-136849237	HIPEpiC	eye:	n/a
26	chr7:136850736-136850786	HepG2	liver:	n/a
27	chr7:136832262-136832312	HIPEpiC	eye:	n/a
28	chr7:136850736-136850786	AG10803	skin:	n/a
29	chr7:136845265-136845315	A549	lung:	n/a
30	chr7:136850736-136850786	HCPEpiC	choroid plexus:	n/a
31	chr7:136850736-136850786	SKMC	muscle:	n/a
32	chr7:136845265-136845315	GM19239	blood:	n/a
33	chr7:136845265-136845315	HRE	kidney:	n/a
34	chr7:136849187-136849237	Jurkat	blood:	n/a
35	chr7:136849143-136849193	SK-N-MC	brain:	n/a
36	chr7:136832262-136832312	HCPEpiC	choroid plexus:	n/a
37	chr7:136849262-136849312	Caco-2	colon:	n/a
38	chr7:136849317-136849367	H1-hESC	embryonic stem cell:	embryo
39	chr7:136879401-136879451	NHDF-neo	bronchial:	n/a
40	chr7:136850736-136850786	NHDF-neo	bronchial:	n/a
41	chr7:136849018-136849068	CMK	blood:	n/a
42	chr7:136832262-136832312	ovcar-3	ovarian:	n/a
43	chr7:136849143-136849193	LNCaP	prostate:	n/a
44	chr7:136849317-136849367	AoSMC	blood vessel:	n/a
45	chr7:136849317-136849367	SK-N-SH	brain:	n/a
46	chr7:136849262-136849312	RPTEC	kidney:	n/a
47	chr7:136850736-136850786	MCF-7	breast:	n/a
48	chr7:136845265-136845315	SK-N-MC	brain:	n/a
49	chr7:136849317-136849367	RPTEC	kidney:	n/a
50	chr7:136849262-136849312	HRPEpiC	eye:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:136858672..136861163-chr7:136864097..136866322,2	K562	blood:
2	chr7:136853692..136854573-chr7:137276894..137277671,4	MCF-7	breast:
3	chr7:136853682..136854530-chr7:137276883..137277639,5	MCF-7	breast:
4	chr2:196521592..196522296-chr7:136849044..136849880,2	HCT-116	colon:
5	chr7:136853684..136854424-chr7:137022605..137023178,2	MCF-7	breast:
6	chr7:136845496..136847194-chr7:136910849..136912754,2	MCF-7	breast:
7	chr4:150815194..150816071-chr7:136849876..136850472,2	MCF-7	breast:
8	chr7:136872945..136874531-chr7:136887427..136890361,2	MCF-7	breast:
9	chr7:136858672..136861163-chr7:136864097..136866322,2	K562	blood:
10	chr7:136854007..136854801-chr7:137137517..137138269,2	MCF-7	breast:
11	chr7:136853835..136854630-chr7:137138677..137139572,6	MCF-7	breast:
12	chr7:136853636..136854568-chr7:137022322..137023760,5	MCF-7	breast:
13	chr7:136853367..136854657-chr7:137138615..137139665,11	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTN-2	chr7:136848868-136849022	ENSG00000234352.5
2	lnc-PTN-2	chr7:136848868-136849088	ENSG00000234352
3	lnc-PTN-2	chr7:136848868-136849022	ENSG00000234352.5
4	lnc-PTN-2	chr7:136848868-136849017	ENSG00000234352.5
5	lnc-PTN-2	chr7:136848868-136849022	ENSG00000234352.5
6	lnc-PTN-2	chr7:136848868-136849017	NONHSAT123574
7	lnc-PTN-2	chr7:136848868-136849020	ENSG00000234352.5
8	lnc-PTN-2	chr7:136866355-136866518	ENSG00000234352
9	lnc-PTN-2	chr7:136848868-136849088	ENSG00000234352.2

No data

Variant related genes	Relation type
ENSG00000224469	TF binding region
ENSG00000234352	TF binding region
ENSG00000224469	CpG island
ENSG00000234352	CpG island
ENSG00000196950	chromatin interactions
ENSG00000157680	chromatin interactions
SLC35B4	miRNA target sites
MUC17	miRNA target sites

Extended variants
information (count: 1173 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1173 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1880792	chr7:136825522-136825523	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs147570068	chr7:136825525-136825526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573072494	chr7:136825529-136825530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551811749	chr7:136825542-136825543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182758057	chr7:136825566-136825567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs534431401	chr7:136825599-136825600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144774711	chr7:136825604-136825605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs4032714	chr7:136825607-136825608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187007275	chr7:136825618-136825619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140706127	chr7:136825644-136825645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150494607	chr7:136825656-136825657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs531455354	chr7:136825657-136825658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs386718228	chr7:136825673-136825674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs373009777	chr7:136825674-136825675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1425077	chr7:136825694-136825695	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs1425076	chr7:136825704-136825705	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs145387107	chr7:136825714-136825715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116450396	chr7:136825715-136825716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560205219	chr7:136825719-136825720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149196750	chr7:136825749-136825750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs1425075	chr7:136825763-136825764	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs28822440	chr7:136825805-136825806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143322294	chr7:136825806-136825807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs35411486	chr7:136825846-136825847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs144874584	chr7:136825921-136825922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191743372	chr7:136825967-136825968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377195393	chr7:136825974-136825975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1593301	chr7:136825987-136825988	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs138950212	chr7:136826032-136826033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140625097	chr7:136826047-136826048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542101924	chr7:136826068-136826069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548048680	chr7:136826069-136826070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs184534777	chr7:136826109-136826110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187779689	chr7:136826140-136826141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs193131529	chr7:136826168-136826169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563858032	chr7:136826173-136826174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569598612	chr7:136826256-136826257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs386718229	chr7:136826269-136826270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1593299	chr7:136826281-136826282	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs568977662	chr7:136826290-136826291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs35655262	chr7:136826384-136826385	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs12667056	chr7:136826409-136826410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1593298	chr7:136826419-136826420	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs568097142	chr7:136826459-136826460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185539738	chr7:136826504-136826505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145689131	chr7:136826508-136826509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138256773	chr7:136826520-136826521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs1593297	chr7:136826568-136826569	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs141818681	chr7:136826633-136826634	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565566381	chr7:136826656-136826657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Neuroticism	17667963	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute myeloid leukemia	17237825	CNVD
Esophageal cancer	21851588	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:157 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136820800-136831200	Weak transcription	NHDF-Ad	bronchial
2	chr7:136825400-136825800	Weak transcription	Rectal Smooth Muscle	rectum
3	chr7:136826600-136826800	Enhancers	HMEC	breast
4	chr7:136826800-136830400	Weak transcription	HMEC	breast
5	chr7:136829600-136830400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:136830000-136830800	Enhancers	NH-A	brain
7	chr7:136830000-136831400	Enhancers	NHLF	lung
8	chr7:136830000-136832000	Enhancers	Muscle Satellite Cultured Cells	--
9	chr7:136830200-136831000	Weak transcription	Rectal Smooth Muscle	rectum
10	chr7:136830200-136831200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr7:136830200-136831200	Enhancers	Osteobl	bone
12	chr7:136830200-136834000	Enhancers	Colon Smooth Muscle	Colon
13	chr7:136830200-136834400	Enhancers	Fetal Heart	heart
14	chr7:136830400-136830600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr7:136830400-136831200	Enhancers	HMEC	breast
16	chr7:136830400-136831400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr7:136830400-136832400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr7:136830400-136832400	Enhancers	HSMM	muscle
19	chr7:136830600-136830800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr7:136830600-136830800	Enhancers	Duodenum Smooth Muscle	Duodenum
21	chr7:136830600-136831800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr7:136830600-136832400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr7:136830600-136833800	Enhancers	Fetal Stomach	stomach
24	chr7:136830800-136831000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr7:136830800-136831000	Flanking Active TSS	NH-A	brain
26	chr7:136830800-136831200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr7:136830800-136833000	Enhancers	HSMMtube	muscle
28	chr7:136830800-136834000	Enhancers	Placenta Amnion	Placenta Amnion
29	chr7:136831000-136831400	Active TSS	NH-A	brain
30	chr7:136831000-136831800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr7:136831000-136832000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr7:136831000-136833000	Enhancers	Rectal Smooth Muscle	rectum
33	chr7:136831200-136831600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr7:136831200-136831800	Flanking Active TSS	HMEC	breast
35	chr7:136831200-136831800	Active TSS	NHDF-Ad	bronchial
36	chr7:136831200-136832000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr7:136831200-136832000	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr7:136831200-136832000	Flanking Active TSS	Osteobl	bone
39	chr7:136831400-136831600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr7:136831400-136831600	Flanking Active TSS	NHLF	lung
41	chr7:136831400-136831800	Flanking Active TSS	NH-A	brain
42	chr7:136831400-136832200	Enhancers	Brain Germinal Matrix	brain
43	chr7:136831400-136832200	Enhancers	Fetal Kidney	kidney
44	chr7:136831400-136833200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr7:136831600-136831800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr7:136831600-136832000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr7:136831600-136832600	Enhancers	NHLF	lung
48	chr7:136831800-136832000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr7:136831800-136832000	Weak transcription	NHDF-Ad	bronchial
50	chr7:136831800-136832400	Enhancers	HMEC	breast

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