Variant report

Variant	nsv831179
Chromosome Location	chr7:144830077-144998851
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:349)
CpG islands
(count:184)
Chromatin interactive
region (count:18)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:349 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:144855243-144855360	K562	blood:	n/a	n/a
2	ATF1	chr7:144875417-144875515	K562	blood:	n/a	n/a
3	ATF1	chr7:144984214-144984301	K562	blood:	n/a	n/a
4	ATF2	chr7:144921921-144922223	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:144878025-144878050	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:144897909-144898047	K562	blood:	n/a	n/a
7	CEBPB	chr7:144840782-144841101	HepG2	liver:	n/a	chr7:144840960-144840971
8	CEBPB	chr7:144869028-144869341	HepG2	liver:	n/a	chr7:144869170-144869181
9	CEBPB	chr7:144869075-144869249	A549	lung:	n/a	chr7:144869170-144869181
10	CEBPB	chr7:144872749-144873032	IMR90	lung:	n/a	chr7:144872879-144872888
11	CEBPB	chr7:144902193-144902510	A549	lung:	n/a	chr7:144902354-144902365
12	CEBPB	chr7:144896927-144897251	HepG2	liver:	n/a	n/a
13	CEBPB	chr7:144855727-144855999	HepG2	liver:	n/a	chr7:144855807-144855818 chr7:144855956-144855967 chr7:144855956-144855969
14	CEBPB	chr7:144896941-144897211	A549	lung:	n/a	n/a
15	CEBPB	chr7:144896976-144897146	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr7:144855776-144855901	A549	lung:	n/a	chr7:144855807-144855818
17	CEBPB	chr7:144913721-144914023	HepG2	liver:	n/a	chr7:144913849-144913866
18	CEBPB	chr7:144843701-144843911	HepG2	liver:	n/a	n/a
19	CEBPB	chr7:144902197-144902536	HepG2	liver:	n/a	chr7:144902354-144902365
20	CHD1	chr7:144880325-144880329	GM12878	blood:	n/a	n/a
21	CTCF	chr7:144867137-144867284	LNCaP	prostate:	n/a	chr7:144867186-144867202 chr7:144867187-144867208
22	CTCF	chr7:144966692-144966713	MCF-7	breast:	n/a	n/a
23	CTCF	chr7:144867000-144867150	NB4	blood:	n/a	n/a
24	CTCF	chr7:144867060-144867210	HRPEpiC	eye:	n/a	chr7:144867186-144867202 chr7:144867187-144867208
25	CTCF	chr7:144986504-144986524	GM20000	blood:	n/a	n/a
26	CTCF	chr7:144849740-144849890	HEK293	kidney:	n/a	n/a
27	CTCF	chr7:144867108-144867279	LNCaP	prostate:	n/a	chr7:144867186-144867202 chr7:144867187-144867208
28	CTCF	chr7:144867147-144867215	Gliobla	brain:	n/a	chr7:144867186-144867202 chr7:144867187-144867208
29	CTCF	chr7:144977254-144977396	K562	blood:	n/a	n/a
30	CTCF	chr7:144867134-144867238	K562	blood:	n/a	chr7:144867186-144867202 chr7:144867187-144867208
31	CTCF	chr7:144867100-144867250	HRPEpiC	eye:	n/a	chr7:144867186-144867202 chr7:144867187-144867208
32	CTCF	chr7:144849854-144849930	MCF-7	breast:	n/a	n/a
33	CTCF	chr7:144965540-144965690	K562	blood:	n/a	n/a
34	CTCF	chr7:144867109-144867245	Hela-S3	cervix:	n/a	chr7:144867186-144867202 chr7:144867187-144867208
35	CTCF	chr7:144849854-144849905	MCF-7	breast:	n/a	n/a
36	CTCF	chr7:144867036-144867309	MCF-7	breast:	n/a	chr7:144867186-144867202 chr7:144867187-144867208
37	CTCF	chr7:144867127-144867234	MCF-7	breast:	n/a	chr7:144867186-144867202 chr7:144867187-144867208
38	CTCF	chr7:144867100-144867250	HPF	lung:	n/a	chr7:144867186-144867202 chr7:144867187-144867208
39	CTCF	chr7:144849737-144849965	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr7:144867156-144867267	GM13977	blood:	n/a	chr7:144867186-144867202 chr7:144867187-144867208
41	CTCF	chr7:144867117-144867238	GM12878	blood:	n/a	chr7:144867186-144867202 chr7:144867187-144867208
42	CTCF	chr7:144867086-144867284	MCF-7	breast:	n/a	chr7:144867186-144867202 chr7:144867187-144867208
43	CTCF	chr7:144867082-144867292	K562	blood:	n/a	chr7:144867186-144867202 chr7:144867187-144867208
44	CTCF	chr7:144849814-144849948	MCF-7	breast:	n/a	n/a
45	CTCF	chr7:144867080-144867230	HEK293	kidney:	n/a	chr7:144867186-144867202 chr7:144867187-144867208
46	CTCF	chr7:144849840-144849990	NB4	blood:	n/a	n/a
47	CTCF	chr7:144867160-144867310	HRE	kidney:	n/a	chr7:144867186-144867202 chr7:144867187-144867208
48	CTCF	chr7:144867123-144867125	Medullo	brain:	n/a	n/a
49	CTCF	chr7:144867128-144867241	Medullo	brain:	n/a	chr7:144867186-144867202 chr7:144867187-144867208
50	CTCF	chr7:144867019-144867350	GM12878	blood:	n/a	chr7:144867186-144867202 chr7:144867187-144867208

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:144967622-144967672	HCPEpiC	choroid plexus:	n/a
2	chr7:144967622-144967672	HCPEpiC	choroid plexus:	n/a
3	chr7:144967385-144967435	HepG2	liver:	n/a
4	chr7:144967622-144967672	SK-N-MC	brain:	n/a
5	chr7:144967385-144967435	U87	brain:	n/a
6	chr7:144967385-144967435	PANC-1	pancreas:	n/a
7	chr7:144966808-144966858	MCF-7	breast:	n/a
8	chr7:144967622-144967672	HRE	kidney:	n/a
9	chr7:144967622-144967672	GM12892	blood:	n/a
10	chr7:144967622-144967672	AG04450	lung:	fetal
11	chr7:144966808-144966858	AG04450	lung:	fetal
12	chr7:144967622-144967672	HL-60	blood:	n/a
13	chr7:144967622-144967672	HRCEpiC	kidney:	n/a
14	chr7:144967622-144967672	U87	brain:	n/a
15	chr7:144966808-144966858	HCM	heart:	n/a
16	chr7:144966808-144966858	HMEC	breast:	n/a
17	chr7:144966808-144966858	A549	lung:	n/a
18	chr7:144967622-144967672	A549	lung:	n/a
19	chr7:144967622-144967672	HRPEpiC	eye:	n/a
20	chr7:144966808-144966858	SAEC	small airway:	n/a
21	chr7:144966808-144966858	HPAEpiC	pulmonary alveolar:	n/a
22	chr7:144966808-144966858	HRE	kidney:	n/a
23	chr7:144967622-144967672	Jurkat	blood:	n/a
24	chr7:144967385-144967435	HAEpiC	amniotic membrane:	n/a
25	chr7:144967385-144967435	T-47D	breast:	n/a
26	chr7:144966808-144966858	GM12892	blood:	n/a
27	chr7:144966808-144966858	SK-N-SH	brain:	n/a
28	chr7:144966808-144966858	AG10803	skin:	n/a
29	chr7:144966808-144966858	ovcar-3	ovarian:	n/a
30	chr7:144966808-144966858	U87	brain:	n/a
31	chr7:144966808-144966858	HNPCEpiC	eye:	n/a
32	chr7:144967622-144967672	Caco-2	colon:	n/a
33	chr7:144967622-144967672	AoSMC	blood vessel:	n/a
34	chr7:144966808-144966858	Jurkat	blood:	n/a
35	chr7:144966808-144966858	PANC-1	pancreas:	n/a
36	chr7:144966808-144966858	SK-N-MC	brain:	n/a
37	chr7:144967622-144967672	NB4	blood:	n/a
38	chr7:144967622-144967672	NT2-D1	testis:	n/a
39	chr7:144967622-144967672	BJ	skin:	n/a
40	chr7:144967622-144967672	SKMC	muscle:	n/a
41	chr7:144967385-144967435	A549	lung:	n/a
42	chr7:144966808-144966858	ProgFib	skin:	n/a
43	chr7:144966808-144966858	Hela-S3	cervix:	n/a
44	chr7:144967385-144967435	PrEC	prostate:	n/a
45	chr7:144966808-144966858	NH-A	brain:	n/a
46	chr7:144966808-144966858	K562	blood:	n/a
47	chr7:144967622-144967672	LNCaP	prostate:	n/a
48	chr7:144966808-144966858	MCF10A-Er-Src	breast:	n/a
49	chr7:144967385-144967435	GM19239	blood:	n/a
50	chr7:144966808-144966858	LNCaP	prostate:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:144530342..144532918-chr7:144881312..144882899,2	K562	blood:
2	chr7:144836936..144838549-chr7:144843546..144845629,2	K562	blood:
3	chr7:144866550..144867305-chr7:145027974..145028611,2	MCF-7	breast:
4	chr7:144841731..144842512-chr7:144850534..144851528,2	MCF-7	breast:
5	chr7:144869840..144872291-chr7:144875754..144877417,2	K562	blood:
6	chr7:144869840..144872291-chr7:144875754..144877417,2	K562	blood:
7	chr7:144964574..144966523-chr7:144993925..144996685,2	K562	blood:
8	chr7:144939623..144941287-chr7:144948474..144950817,2	MCF-7	breast:
9	chr7:144866805..144867709-chr7:145027906..145028706,4	MCF-7	breast:
10	chr7:144886766..144888686-chr7:144890231..144891903,2	K562	blood:
11	chr7:144831796..144834565-chr7:144835834..144837604,2	MCF-7	breast:
12	chr7:144841731..144842512-chr7:144850534..144851528,2	MCF-7	breast:
13	chr7:144939623..144941287-chr7:144948474..144950817,2	MCF-7	breast:
14	chr7:144964574..144966523-chr7:144993925..144996685,2	K562	blood:
15	chr7:144836936..144838549-chr7:144843546..144845629,2	K562	blood:
16	chr7:144831796..144834565-chr7:144835834..144837604,2	MCF-7	breast:
17	chr7:144886766..144888686-chr7:144890231..144891903,2	K562	blood:
18	chr7:144849072..144851097-chr7:146354909..146357646,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARHGEF5-2	chr7:144854027-144854051	NONHSAT123937
2	lnc-ARHGEF5-2	chr7:144854028-144854153	XLOC_006283
3	lnc-ARHGEF5-2	chr7:144857165-144857237	XLOC_006283
4	lnc-ARHGEF5-2	chr7:144854106-144854153	XLOC_006283
5	lnc-ARHGEF5-2	chr7:144855171-144855285	XLOC_006283
6	lnc-ARHGEF5-2	chr7:144854028-144854051	XLOC_006283
7	lnc-ARHGEF5-2	chr7:144857165-144857358	XLOC_006283
8	lnc-ARHGEF5-2	chr7:144854028-144854153	XLOC_006283
9	lnc-ARHGEF5-2	chr7:144855973-144856107	XLOC_006283

No data

Variant related genes	Relation type
ENSG00000226592	TF binding region
ENSG00000226592	CpG island
ARL6IP5	miRNA target sites
ROBO2	miRNA target sites
FZD7	miRNA target sites
CCKBR	miRNA target sites

Extended variants
information (count: 1840 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1840 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7778188	chr7:144833408-144833409	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs528425104	chr7:144833423-144833424	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs564115785	chr7:144833515-144833516	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs145807977	chr7:144833563-144833564	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs148989292	chr7:144833593-144833594	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs546918209	chr7:144833617-144833618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs117403251	chr7:144833630-144833631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188983754	chr7:144833632-144833633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs367685100	chr7:144833637-144833638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs143065981	chr7:144833658-144833659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs148212308	chr7:144833710-144833711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555731207	chr7:144833716-144833717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567938065	chr7:144833730-144833731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529138359	chr7:144833867-144833868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553703448	chr7:144833873-144833874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs35656126	chr7:144833942-144833943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs398086232	chr7:144833943-144833944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs397716481	chr7:144833944-144833945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs193112048	chr7:144834041-144834042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183547338	chr7:144834106-144834107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557473217	chr7:144834175-144834176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575680190	chr7:144834187-144834188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs6464650	chr7:144834191-144834192	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs560968364	chr7:144834230-144834231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs140295918	chr7:144834238-144834239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536411137	chr7:144834282-144834283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs199708946	chr7:144834334-144834335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564859680	chr7:144834356-144834357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs111607029	chr7:144834362-144834363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554451221	chr7:144834383-144834384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531947007	chr7:144834469-144834470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550196581	chr7:144834500-144834501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145194961	chr7:144834502-144834503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7801954	chr7:144834503-144834504	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs623768	chr7:144834513-144834514	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs527338	chr7:144834563-144834564	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs187397281	chr7:144834609-144834610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs623305	chr7:144834619-144834620	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs577870625	chr7:144834641-144834642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191524675	chr7:144834701-144834702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183960690	chr7:144834787-144834788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112315721	chr7:144834846-144834847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs556058732	chr7:144834850-144834851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs611224	chr7:144834930-144834931	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs553512659	chr7:144834961-144834962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs188735023	chr7:144834977-144834978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs192648251	chr7:144835033-144835034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7784261	chr7:144835036-144835037	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs77249244	chr7:144835091-144835092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572925767	chr7:144835097-144835098	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
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
Splenic marginal zone lymphoma	21957467	CNVD
Glioblastoma multiforme	18628472	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	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pancreatitis	21956041	CNVD
Acute myeloid leukemia	16864856	CNVD
Gastric cancer	16891809	CNVD
Lung cancer	17086460	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:144833400-144833600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:144833600-144844000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr7:144834800-144835000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:144835200-144836400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:144836400-144836800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr7:144836800-144839200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:144838800-144839800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr7:144839200-144840200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr7:144839400-144840000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr7:144839400-144840000	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr7:144839600-144840200	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr7:144839600-144840600	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr7:144840000-144843600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr7:144840600-144841000	Enhancers	Adipose Nuclei	Adipose
15	chr7:144841000-144842000	Weak transcription	Adipose Nuclei	Adipose
16	chr7:144842000-144842200	Enhancers	Adipose Nuclei	Adipose
17	chr7:144843600-144844000	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr7:144844000-144844200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr7:144854400-144855400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr7:144856800-144857400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr7:144857200-144860800	Weak transcription	Psoas Muscle	Psoas
22	chr7:144857400-144860000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr7:144860000-144860200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr7:144860000-144860200	Enhancers	Pancreas	Pancrea
25	chr7:144860200-144860600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr7:144860200-144860600	Enhancers	Adipose Nuclei	Adipose
27	chr7:144860400-144860600	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr7:144860600-144860800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr7:144860600-144863000	Weak transcription	Adipose Nuclei	Adipose
30	chr7:144863000-144863800	Enhancers	Adipose Nuclei	Adipose
31	chr7:144866000-144866400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr7:144866200-144867600	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr7:144871600-144873800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr7:144872000-144872400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr7:144902400-144902800	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr7:144902400-144902800	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr7:144906800-144907000	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr7:144907000-144908000	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr7:144908000-144910000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr7:144908000-144910000	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr7:144909000-144910200	Enhancers	Adipose Nuclei	Adipose
42	chr7:144909000-144910400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr7:144909200-144909400	Enhancers	Brain Cingulate Gyrus	brain
44	chr7:144909400-144910000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr7:144909400-144910200	Enhancers	Brain Angular Gyrus	brain
46	chr7:144914000-144914400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr7:144916400-144917000	Enhancers	Adipose Nuclei	Adipose
48	chr7:144916600-144916800	Enhancers	Right Atrium	heart
49	chr7:144921000-144923000	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr7:144921200-144922400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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