Variant report

Variant	nsv887811
Chromosome Location	chr7:18295790-18346230
allele	n/a
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	ARID3A	chr7:18303709-18303826	K562	blood:	n/a	n/a
2	ATF1	chr7:18301886-18302085	K562	blood:	n/a	n/a
3	ATF1	chr7:18329927-18330098	K562	blood:	n/a	n/a
4	BHLHE40	chr7:18335718-18335912	GM12878	blood:	n/a	chr7:18335758-18335779 chr7:18335763-18335772
5	CBX3	chr7:18301669-18302135	K562	blood:	n/a	n/a
6	CBX3	chr7:18301668-18302097	K562	blood:	n/a	n/a
7	CBX3	chr7:18301694-18302044	HCT-116	colon:	n/a	n/a
8	CBX3	chr7:18301664-18302173	HCT-116	colon:	n/a	n/a
9	CEBPB	chr7:18328293-18328580	Hela-S3	cervix:	n/a	chr7:18328443-18328454 chr7:18328442-18328455
10	CEBPB	chr7:18328324-18328535	HepG2	liver:	n/a	chr7:18328443-18328454 chr7:18328442-18328455
11	CEBPB	chr7:18329191-18329470	HepG2	liver:	n/a	chr7:18329301-18329312 chr7:18329301-18329314 chr7:18329339-18329352
12	CEBPB	chr7:18329174-18329463	IMR90	lung:	n/a	chr7:18329301-18329312 chr7:18329301-18329314 chr7:18329339-18329352
13	CEBPB	chr7:18330610-18330810	IMR90	lung:	n/a	chr7:18330738-18330751
14	CEBPB	chr7:18329159-18329444	K562	blood:	n/a	chr7:18329301-18329312 chr7:18329301-18329314 chr7:18329339-18329352
15	CEBPB	chr7:18328327-18328538	K562	blood:	n/a	chr7:18328443-18328454 chr7:18328442-18328455
16	CEBPB	chr7:18305549-18305889	HepG2	liver:	n/a	chr7:18305697-18305708
17	CEBPB	chr7:18305670-18305763	Hela-S3	cervix:	n/a	chr7:18305697-18305708
18	CEBPB	chr7:18329159-18329461	Hela-S3	cervix:	n/a	chr7:18329301-18329312 chr7:18329301-18329314 chr7:18329339-18329352
19	CEBPB	chr7:18322258-18322423	HepG2	liver:	n/a	chr7:18322289-18322300
20	CEBPB	chr7:18329213-18329481	H1-hESC	embryonic stem cell:	n/a	chr7:18329301-18329312 chr7:18329301-18329314 chr7:18329339-18329352
21	CEBPB	chr7:18329187-18329443	A549	lung:	n/a	chr7:18329301-18329312 chr7:18329301-18329314 chr7:18329339-18329352
22	CEBPB	chr7:18305535-18305883	K562	blood:	n/a	chr7:18305697-18305708
23	CEBPB	chr7:18330547-18330801	Hela-S3	cervix:	n/a	chr7:18330738-18330751
24	CEBPB	chr7:18305535-18305862	IMR90	lung:	n/a	chr7:18305697-18305708
25	CEBPB	chr7:18305544-18305869	A549	lung:	n/a	chr7:18305697-18305708
26	CEBPB	chr7:18330539-18330822	K562	blood:	n/a	chr7:18330738-18330751
27	CEBPB	chr7:18329956-18330146	K562	blood:	n/a	n/a
28	CEBPB	chr7:18329208-18329413	ECC-1	luminal epithelium:	n/a	chr7:18329301-18329312 chr7:18329301-18329314 chr7:18329339-18329352
29	CEBPB	chr7:18297423-18297513	IMR90	lung:	n/a	chr7:18297442-18297453 chr7:18297440-18297453
30	CREB1	chr7:18297481-18297699	GM12878	blood:	n/a	n/a
31	CTCF	chr7:18335796-18335882	Lung_OC	lung:	n/a	chr7:18335831-18335844
32	CTCF	chr7:18316206-18316272	GM12878	blood:	n/a	chr7:18316243-18316259 chr7:18316244-18316265
33	CTCF	chr7:18316179-18316306	HUVEC	blood vessel:	n/a	chr7:18316243-18316259 chr7:18316244-18316265
34	CTCF	chr7:18335800-18335950	AG09319	gingival:	n/a	chr7:18335831-18335844
35	CTCF	chr7:18316120-18316270	AoAF	blood vessel:	n/a	chr7:18316243-18316259 chr7:18316244-18316265
36	CTCF	chr7:18335806-18335950	GM12878	blood:	n/a	chr7:18335831-18335844
37	CTCF	chr7:18316194-18316286	K562	blood:	n/a	chr7:18316243-18316259 chr7:18316244-18316265
38	CTCF	chr7:18316170-18316301	LNCaP	prostate:	n/a	chr7:18316243-18316259 chr7:18316244-18316265
39	CTCF	chr7:18335828-18335865	GM12878	blood:	n/a	chr7:18335831-18335844
40	CTCF	chr7:18316120-18316270	HEK293	kidney:	n/a	chr7:18316243-18316259 chr7:18316244-18316265
41	CTCF	chr7:18316120-18316270	AG09319	gingival:	n/a	chr7:18316243-18316259 chr7:18316244-18316265
42	CTCF	chr7:18316140-18316290	HCPEpiC	choroid plexus:	n/a	chr7:18316243-18316259 chr7:18316244-18316265
43	CTCF	chr7:18316100-18316250	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr7:18316180-18316330	MCF-7	breast:	n/a	chr7:18316243-18316259 chr7:18316244-18316265
45	CTCF	chr7:18316180-18316330	HRPEpiC	eye:	n/a	chr7:18316243-18316259 chr7:18316244-18316265
46	CTCF	chr7:18316160-18316310	HMEC	breast:	n/a	chr7:18316243-18316259 chr7:18316244-18316265
47	CTCF	chr7:18316200-18316350	HMF	breast:	n/a	chr7:18316243-18316259 chr7:18316244-18316265
48	CTCF	chr7:18335780-18335930	MCF-7	breast:	n/a	chr7:18335831-18335844
49	CTCF	chr7:18335824-18335875	GM10248	blood:	n/a	chr7:18335831-18335844
50	CTCF	chr7:18316160-18316310	GM12874	blood:	n/a	chr7:18316243-18316259 chr7:18316244-18316265

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:18329916-18329966	BE2_C	brain:	n/a
2	chr7:18329916-18329966	BE2_C	brain:	n/a
3	chr7:18330092-18330142	HCT-116	colon:	n/a
4	chr7:18329602-18329652	HUVEC	blood vessel:	n/a
5	chr7:18329562-18329612	HL-60	blood:	n/a
6	chr7:18329562-18329612	AG04449	skin:	fetal
7	chr7:18329602-18329652	HCF	heart:	n/a
8	chr7:18329602-18329652	HRE	kidney:	n/a
9	chr7:18329916-18329966	Hela-S3	cervix:	n/a
10	chr7:18330092-18330142	BJ	skin:	n/a
11	chr7:18329916-18329966	HCPEpiC	choroid plexus:	n/a
12	chr7:18330092-18330142	HMEC	breast:	n/a
13	chr7:18329602-18329652	HepG2	liver:	n/a
14	chr7:18330092-18330142	AG09319	gingival:	n/a
15	chr7:18330092-18330142	IMR90	lung:	fetal
16	chr7:18329562-18329612	K562	blood:	n/a
17	chr7:18329916-18329966	NHDF-neo	bronchial:	n/a
18	chr7:18330092-18330142	HEK293	kidney:	embryo
19	chr7:18330092-18330142	U87	brain:	n/a
20	chr7:18330092-18330142	HUVEC	blood vessel:	n/a
21	chr7:18329916-18329966	NH-A	brain:	n/a
22	chr7:18330092-18330142	SKMC	muscle:	n/a
23	chr7:18330092-18330142	GM12878	blood:	n/a
24	chr7:18329562-18329612	PANC-1	pancreas:	n/a
25	chr7:18329916-18329966	HUVEC	blood vessel:	n/a
26	chr7:18329562-18329612	Caco-2	colon:	n/a
27	chr7:18330092-18330142	HRCEpiC	kidney:	n/a
28	chr7:18329602-18329652	HCM	heart:	n/a
29	chr7:18330092-18330142	PANC-1	pancreas:	n/a
30	chr7:18329602-18329652	GM12878	blood:	n/a
31	chr7:18329562-18329612	ovcar-3	ovarian:	n/a
32	chr7:18329916-18329966	Caco-2	colon:	n/a
33	chr7:18329562-18329612	AG04450	lung:	fetal
34	chr7:18330092-18330142	HIPEpiC	eye:	n/a
35	chr7:18330092-18330142	HEEpiC	esophagus:	n/a
36	chr7:18329602-18329652	HRCEpiC	kidney:	n/a
37	chr7:18329602-18329652	U87	brain:	n/a
38	chr7:18330092-18330142	HNPCEpiC	eye:	n/a
39	chr7:18329562-18329612	HMEC	breast:	n/a
40	chr7:18329916-18329966	AG10803	skin:	n/a
41	chr7:18329916-18329966	CMK	blood:	n/a
42	chr7:18329562-18329612	MCF-7	breast:	n/a
43	chr7:18329916-18329966	AG04449	skin:	fetal
44	chr7:18329916-18329966	AG09319	gingival:	n/a
45	chr7:18329602-18329652	AG09309	skin:	n/a
46	chr7:18329562-18329612	PFSK-1	brain:	n/a
47	chr7:18329602-18329652	HL-60	blood:	n/a
48	chr7:18329916-18329966	U87	brain:	n/a
49	chr7:18329916-18329966	HL-60	blood:	n/a
50	chr7:18329916-18329966	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:18311330..18313091-chr7:18314736..18317305,2	K562	blood:
2	chr7:18285502..18287051-chr7:18294560..18297102,2	MCF-7	breast:
3	chr7:18311330..18313091-chr7:18314736..18317305,2	K562	blood:
4	chr7:18310468..18313091-chr7:18314736..18317253,2	K562	blood:
5	chr7:18310468..18313091-chr7:18314736..18317253,2	K562	blood:
6	chr7:18338973..18341007-chr7:18351398..18353885,2	K562	blood:
7	chr7:18325772..18327455-chr7:18347556..18349575,2	K562	blood:
8	chr7:18250651..18253317-chr7:18302876..18305651,2	K562	blood:
9	chr7:18321787..18324563-chr7:18327488..18329360,2	K562	blood:
10	chr7:18321787..18324563-chr7:18327488..18329360,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AHR-8	chr7:18330064-18330138	NONHSAT119359
2	lnc-AHR-8	chr7:18330073-18330138	NONHSAT119360
3	lnc-AHR-8	chr7:18329811-18329970	NONHSAT119359

Variant related genes	Relation type
ENSG00000223030	TF binding region
HDAC9	TF binding region
ENSG00000223030	CpG island
HDAC9	CpG island

Extended variants
information (count: 1264 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1264 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576430425	chr7:18297433-18297434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs17138874	chr7:18297439-18297440	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs556642728	chr7:18297445-18297446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187064532	chr7:18297451-18297452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545495333	chr7:18297495-18297496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560448321	chr7:18297536-18297537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs57820243	chr7:18297581-18297582	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs376184653	chr7:18297658-18297659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs191702143	chr7:18297668-18297669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs111779849	chr7:18297672-18297673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs561229937	chr7:18297782-18297783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540091927	chr7:18297805-18297806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs183598818	chr7:18297815-18297816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549361345	chr7:18297845-18297846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142521619	chr7:18297893-18297894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs532067849	chr7:18297900-18297901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs10236170	chr7:18297903-18297904	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs371348004	chr7:18297919-18297920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76749757	chr7:18297937-18297938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188936098	chr7:18297940-18297941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs554847798	chr7:18297952-18297953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs117919718	chr7:18297953-18297954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537348448	chr7:18297987-18297988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556559023	chr7:18297988-18297989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189027833	chr7:18311214-18311215	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs535555591	chr7:18311230-18311231	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs181653661	chr7:18311234-18311235	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs575371336	chr7:18311249-18311250	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs547871730	chr7:18311266-18311267	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs557620324	chr7:18311274-18311275	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs572846678	chr7:18311301-18311302	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs187615762	chr7:18311308-18311309	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs548097752	chr7:18311335-18311336	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs191936424	chr7:18311350-18311351	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs543412784	chr7:18311399-18311400	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs563665904	chr7:18311407-18311408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs139409423	chr7:18311427-18311428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552852346	chr7:18311457-18311458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571111123	chr7:18311485-18311486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs527962107	chr7:18311488-18311489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528806308	chr7:18311526-18311527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547711680	chr7:18311570-18311571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568072179	chr7:18311574-18311575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs111978	chr7:18311577-18311578	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs181074608	chr7:18311628-18311629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539603363	chr7:18311664-18311665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185323279	chr7:18311677-18311678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189684454	chr7:18311678-18311679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556342489	chr7:18311680-18311681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs74417058	chr7:18311711-18311712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Sezary syndrome	18413736	CNVD
Bipolar disorder	19114987	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:187 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:18297400-18298000	Enhancers	HUVEC	blood vessel
2	chr7:18311200-18311400	ZNF genes & repeats	Aorta	Aorta
3	chr7:18311400-18315000	Weak transcription	Aorta	Aorta
4	chr7:18314600-18315000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr7:18315000-18315200	Enhancers	Aorta	Aorta
6	chr7:18317600-18317800	Enhancers	Rectal Smooth Muscle	rectum
7	chr7:18317600-18318000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr7:18317800-18318200	Enhancers	Colon Smooth Muscle	Colon
9	chr7:18317800-18318600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr7:18320600-18321600	Enhancers	Fetal Heart	heart
11	chr7:18321600-18328600	Weak transcription	Fetal Heart	heart
12	chr7:18322400-18323200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
13	chr7:18325400-18325800	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr7:18325800-18326800	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr7:18326800-18327200	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr7:18327200-18328400	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr7:18327200-18329800	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr7:18327200-18332000	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr7:18327400-18328800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr7:18327400-18329200	Enhancers	Primary B cells from cord blood	blood
21	chr7:18327800-18329400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr7:18328000-18329400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr7:18328000-18329800	Enhancers	Primary B cells from peripheral blood	blood
24	chr7:18328200-18328400	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr7:18328400-18328600	Enhancers	Primary T cells fromperipheralblood	blood
26	chr7:18328400-18328600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr7:18328400-18328800	Enhancers	Fetal Thymus	thymus
28	chr7:18328400-18328800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr7:18328400-18329200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr7:18328400-18329400	Enhancers	Primary hematopoietic stem cells	blood
31	chr7:18328600-18329400	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr7:18328600-18329400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr7:18328600-18330200	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr7:18328600-18332200	Enhancers	Fetal Heart	heart
35	chr7:18328800-18329200	Weak transcription	Fetal Thymus	thymus
36	chr7:18328800-18329200	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr7:18328800-18330000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
38	chr7:18329200-18329600	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr7:18329200-18329800	Enhancers	Brain Germinal Matrix	brain
40	chr7:18329200-18330000	Enhancers	Fetal Thymus	thymus
41	chr7:18329200-18330000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
42	chr7:18329200-18330200	Flanking Active TSS	Primary B cells from cord blood	blood
43	chr7:18329200-18330200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr7:18329200-18331600	Enhancers	Small Intestine	intestine
45	chr7:18329400-18329600	Enhancers	Primary T cells fromperipheralblood	blood
46	chr7:18329400-18329800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr7:18329400-18329800	Active TSS	GM12878-XiMat	blood
48	chr7:18329400-18330600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr7:18329400-18330800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
50	chr7:18329400-18332600	Flanking Active TSS	Primary hematopoietic stem cells	blood

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