Variant report

Variant	nsv887318
Chromosome Location	chr7:3099853-3127784
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:531)
CpG islands
(count:61)
Chromatin interactive
region (count:22)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:531 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:3105497-3105652	K562	blood:	n/a	n/a
2	ATF1	chr7:3106942-3107186	K562	blood:	n/a	n/a
3	ATF2	chr7:3106806-3107600	GM12878	blood:	n/a	n/a
4	ATF2	chr7:3105291-3105895	GM12878	blood:	n/a	chr7:3105618-3105629
5	ATF2	chr7:3105231-3105773	H1-hESC	embryonic stem cell:	n/a	chr7:3105618-3105629
6	ATF2	chr7:3105272-3105905	GM12878	blood:	n/a	chr7:3105618-3105629
7	ATF2	chr7:3118024-3118508	GM12878	blood:	n/a	n/a
8	ATF2	chr7:3105203-3105795	H1-hESC	embryonic stem cell:	n/a	chr7:3105618-3105629
9	ATF2	chr7:3106829-3107344	GM12878	blood:	n/a	n/a
10	ATF2	chr7:3118056-3118550	GM12878	blood:	n/a	n/a
11	ATF2	chr7:3108148-3108734	GM12878	blood:	n/a	n/a
12	ATF2	chr7:3108146-3108703	GM12878	blood:	n/a	n/a
13	ATF3	chr7:3105336-3105721	K562	blood:	n/a	n/a
14	ATF3	chr7:3106922-3107172	GM12878	blood:	n/a	n/a
15	BACH1	chr7:3105352-3105669	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr7:3118166-3118517	GM12878	blood:	n/a	n/a
17	BATF	chr7:3108295-3108545	GM12878	blood:	n/a	n/a
18	BATF	chr7:3102652-3102984	GM12878	blood:	n/a	chr7:3102817-3102828
19	BATF	chr7:3107333-3107645	GM12878	blood:	n/a	n/a
20	BATF	chr7:3114599-3114890	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:3105376-3105861	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:3108267-3108567	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:3118127-3118458	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:3118124-3118494	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:3108184-3108629	GM12878	blood:	n/a	n/a
26	BCLAF1	chr7:3102522-3103033	GM12878	blood:	n/a	n/a
27	BCLAF1	chr7:3105271-3105749	GM12878	blood:	n/a	n/a
28	BHLHE40	chr7:3126085-3126131	K562	blood:	n/a	n/a
29	BHLHE40	chr7:3120025-3120105	K562	blood:	n/a	n/a
30	BHLHE40	chr7:3107943-3107999	GM12878	blood:	n/a	n/a
31	BHLHE40	chr7:3118443-3118622	K562	blood:	n/a	n/a
32	BHLHE40	chr7:3122367-3122715	K562	blood:	n/a	chr7:3122437-3122446
33	BHLHE40	chr7:3106998-3107263	GM12878	blood:	n/a	n/a
34	BHLHE40	chr7:3105381-3105678	K562	blood:	n/a	n/a
35	BHLHE40	chr7:3106940-3107212	K562	blood:	n/a	n/a
36	BHLHE40	chr7:3108257-3108558	GM12878	blood:	n/a	n/a
37	BHLHE40	chr7:3118138-3118639	GM12878	blood:	n/a	n/a
38	CBX3	chr7:3105340-3105693	K562	blood:	n/a	n/a
39	CEBPB	chr7:3109700-3110064	A549	lung:	n/a	chr7:3109883-3109894
40	CEBPB	chr7:3109745-3110027	H1-hESC	embryonic stem cell:	n/a	chr7:3109883-3109894
41	CEBPB	chr7:3115189-3115491	K562	blood:	n/a	chr7:3115311-3115322
42	CEBPB	chr7:3109775-3110077	K562	blood:	n/a	chr7:3109883-3109894
43	CEBPB	chr7:3108232-3108401	H1-hESC	embryonic stem cell:	n/a	chr7:3108298-3108309
44	CEBPB	chr7:3116404-3116590	HepG2	liver:	n/a	n/a
45	CEBPB	chr7:3105483-3105621	K562	blood:	n/a	n/a
46	CEBPB	chr7:3108191-3108463	Hela-S3	cervix:	n/a	chr7:3108298-3108309
47	CEBPB	chr7:3108263-3108392	K562	blood:	n/a	chr7:3108298-3108309
48	CEBPB	chr7:3108165-3108448	IMR90	lung:	n/a	chr7:3108298-3108309
49	CEBPB	chr7:3115199-3115474	IMR90	lung:	n/a	chr7:3115311-3115322
50	CEBPB	chr7:3109705-3110068	HepG2	liver:	n/a	chr7:3109883-3109894

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3127028-3127078	HAEpiC	amniotic membrane:	n/a
2	chr7:3127028-3127078	CMK	blood:	n/a
3	chr7:3127028-3127078	HEK293	kidney:	embryo
4	chr7:3127028-3127078	NHBE	bronchial:	n/a
5	chr7:3127028-3127078	A549	lung:	n/a
6	chr7:3127028-3127078	MCF-7	breast:	n/a
7	chr7:3127028-3127078	SK-N-MC	brain:	n/a
8	chr7:3127028-3127078	Hela-S3	cervix:	n/a
9	chr7:3127028-3127078	NH-A	brain:	n/a
10	chr7:3127028-3127078	GM12892	blood:	n/a
11	chr7:3127028-3127078	SK-N-SH	brain:	n/a
12	chr7:3127028-3127078	HCT-116	colon:	n/a
13	chr7:3127028-3127078	GM12878	blood:	n/a
14	chr7:3127028-3127078	Hepatocyte	liver:	n/a
15	chr7:3127028-3127078	AG04450	lung:	fetal
16	chr7:3127028-3127078	Jurkat	blood:	n/a
17	chr7:3127028-3127078	MCF10A-Er-Src	breast:	n/a
18	chr7:3127028-3127078	HEEpiC	esophagus:	n/a
19	chr7:3127028-3127078	HNPCEpiC	eye:	n/a
20	chr7:3127028-3127078	HCM	heart:	n/a
21	chr7:3127028-3127078	GM06990	blood:	n/a
22	chr7:3127028-3127078	AG04449	skin:	fetal
23	chr7:3127028-3127078	K562	blood:	n/a
24	chr7:3127028-3127078	RPTEC	kidney:	n/a
25	chr7:3127028-3127078	NT2-D1	testis:	n/a
26	chr7:3127028-3127078	IMR90	lung:	fetal
27	chr7:3127028-3127078	HMEC	breast:	n/a
28	chr7:3127028-3127078	SAEC	small airway:	n/a
29	chr7:3127028-3127078	T-47D	breast:	n/a
30	chr7:3127028-3127078	HUVEC	blood vessel:	n/a
31	chr7:3127028-3127078	Caco-2	colon:	n/a
32	chr7:3127028-3127078	SK-N-SH_RA	brain:	n/a
33	chr7:3127028-3127078	BE2_C	brain:	n/a
34	chr7:3127028-3127078	GM19239	blood:	n/a
35	chr7:3127028-3127078	NHDF-neo	bronchial:	n/a
36	chr7:3127028-3127078	AG09319	gingival:	n/a
37	chr7:3127028-3127078	NB4	blood:	n/a
38	chr7:3127028-3127078	HRPEpiC	eye:	n/a
39	chr7:3127028-3127078	HCF	heart:	n/a
40	chr7:3127028-3127078	BJ	skin:	n/a
41	chr7:3127028-3127078	ECC-1	luminal epithelium:	n/a
42	chr7:3127028-3127078	HPAEpiC	pulmonary alveolar:	n/a
43	chr7:3127028-3127078	PrEC	prostate:	n/a
44	chr7:3127028-3127078	HRE	kidney:	n/a
45	chr7:3127028-3127078	HCPEpiC	choroid plexus:	n/a
46	chr7:3127028-3127078	AG09309	skin:	n/a
47	chr7:3127028-3127078	AoSMC	blood vessel:	n/a
48	chr7:3127028-3127078	U87	brain:	n/a
49	chr7:3127028-3127078	HL-60	blood:	n/a
50	chr7:3127028-3127078	GM12891	blood:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:58240265..58241060-chr7:3105189..3105924,2	MCF-7	breast:
2	chr7:2913414..2914953-chr7:3113951..3116529,2	MCF-7	breast:
3	chr2:72221976..72222488-chr7:3105454..3105962,2	MCF-7	breast:
4	chr7:3114729..3116313-chr7:3116448..3118369,2	MCF-7	breast:
5	chr7:3113104..3115838-chr7:3115974..3117943,2	K562	blood:
6	chr7:3102265..3103829-chr7:3107588..3109384,2	MCF-7	breast:
7	chr7:2926548..2927187-chr7:3103632..3104310,2	MCF-7	breast:
8	chr7:3102265..3103829-chr7:3107588..3109384,2	MCF-7	breast:
9	chr7:2926330..2927157-chr7:3107129..3108063,2	K562	blood:
10	chr7:3093019..3096791-chr7:3101830..3105746,3	MCF-7	breast:
11	chr17:56735316..56738174-chr7:3105688..3107958,2	MCF-7	breast:
12	chr7:2911909..2914760-chr7:3102455..3104497,2	MCF-7	breast:
13	chr7:3105018..3105890-chr7:3193882..3195188,3	MCF-7	breast:
14	chr7:3104949..3105997-chr7:3194351..3195035,3	MCF-7	breast:
15	chr7:3114729..3116313-chr7:3116448..3118369,2	MCF-7	breast:
16	chr7:3105046..3105933-chr7:3194248..3194999,3	K562	blood:
17	chr7:2926382..2927118-chr7:3105405..3105996,2	MCF-7	breast:
18	chr7:3095854..3098003-chr7:3113268..3116037,2	K562	blood:
19	chr7:3113104..3115838-chr7:3115974..3117943,2	K562	blood:
20	chr7:2913908..2916162-chr7:3122594..3124369,2	MCF-7	breast:
21	chr7:2904486..2905293-chr7:3103659..3104561,2	MCF-7	breast:
22	chr7:3104998..3105685-chr7:3239854..3240733,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CARD11-1	chr7:3122886-3123252	XLOC_006337
2	lnc-CARD11-3	chr7:3124135-3124176	l_3354_chr7:3100290-3107234_whiteBloodCell
3	lnc-CARD11-3	chr7:3100291-3101745	l_3354_chr7:3100290-3107234_whiteBloodCell
4	lnc-CARD11-3	chr7:3107182-3107234	l_3354_chr7:3100290-3107234_whiteBloodCell
5	lnc-CARD11-1	chr7:3125986-3126055	XLOC_006337

No data

Variant related genes	Relation type
ENSG00000228334	TF binding region
ENSG00000228334	CpG island
ENSG00000202077	chromatin interactions

Extended variants
information (count: 1308 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1308 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62439357	chr7:3100205-3100206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs144653421	chr7:3100220-3100221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs368864690	chr7:3100225-3100226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78328693	chr7:3100288-3100289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs181815979	chr7:3100290-3100291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs542309144	chr7:3100337-3100338	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs138538043	chr7:3100365-3100366	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs576124439	chr7:3100366-3100367	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs554740774	chr7:3100368-3100369	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs545312348	chr7:3100394-3100395	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs574098924	chr7:3100417-3100418	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs565015007	chr7:3100433-3100434	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs141494984	chr7:3100436-3100437	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs556319601	chr7:3100452-3100453	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs145570938	chr7:3100461-3100462	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs529412092	chr7:3100561-3100562	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs549173629	chr7:3100588-3100589	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs187668992	chr7:3100611-3100612	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs531789594	chr7:3100682-3100683	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs552086220	chr7:3100698-3100699	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs376509600	chr7:3100725-3100726	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs566615874	chr7:3100731-3100732	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs571596712	chr7:3100746-3100747	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs533586350	chr7:3100781-3100782	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs546990625	chr7:3100792-3100793	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs74442764	chr7:3100805-3100806	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs372764617	chr7:3100824-3100825	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs2396967	chr7:3100838-3100839	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs115755482	chr7:3100842-3100843	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs538442369	chr7:3100862-3100863	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs558934758	chr7:3100871-3100872	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs201633830	chr7:3100934-3100935	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs187762215	chr7:3100939-3100940	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs200564024	chr7:3100940-3100941	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs7459191	chr7:3100942-3100943	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs7459192	chr7:3100944-3100945	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs374495889	chr7:3100946-3100947	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs376576020	chr7:3100948-3100949	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs2396966	chr7:3100950-3100951	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs2396965	chr7:3100952-3100953	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs377166752	chr7:3100966-3100967	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs200166621	chr7:3100968-3100969	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs146320665	chr7:3100970-3100971	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs71029615	chr7:3100971-3100972	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs138648805	chr7:3100972-3100973	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs11760567	chr7:3100977-3100978	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs541282184	chr7:3100990-3100991	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs138112831	chr7:3100994-3100995	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs573922396	chr7:3101012-3101013	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs149533962	chr7:3101052-3101053	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	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
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Nasopharyngeal cancer	20548289	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:164 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3100200-3100400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
2	chr7:3100800-3102000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr7:3102000-3102200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
4	chr7:3102000-3102400	Enhancers	Primary T cells fromperipheralblood	blood
5	chr7:3102000-3102400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
6	chr7:3102000-3102400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr7:3102000-3102400	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr7:3102000-3102400	Enhancers	Primary T helper cells fromperipheralblood	blood
9	chr7:3102000-3102400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr7:3102000-3102600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr7:3102000-3113800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
12	chr7:3102200-3102400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr7:3102200-3102400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr7:3102200-3102400	Enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr7:3102200-3102600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr7:3102200-3102600	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr7:3102200-3103000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
18	chr7:3102400-3102600	Enhancers	Primary T cells from cord blood	blood
19	chr7:3102400-3102600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
20	chr7:3102400-3102600	Enhancers	GM12878-XiMat	blood
21	chr7:3102400-3102800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr7:3102400-3103200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
23	chr7:3102400-3103200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
24	chr7:3102400-3103200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
25	chr7:3102400-3103200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
26	chr7:3102400-3103200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
27	chr7:3102400-3103400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
28	chr7:3102400-3103400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
29	chr7:3102400-3103600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
30	chr7:3102400-3103800	Enhancers	Primary B cells from peripheral blood	blood
31	chr7:3102400-3106000	Enhancers	Fetal Thymus	thymus
32	chr7:3102600-3102800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
33	chr7:3102600-3103000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
34	chr7:3102600-3103200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
35	chr7:3102600-3103200	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
36	chr7:3102600-3103400	Flanking Active TSS	GM12878-XiMat	blood
37	chr7:3102600-3103600	Flanking Active TSS	Primary T cells from cord blood	blood
38	chr7:3102600-3109800	Enhancers	Primary B cells from cord blood	blood
39	chr7:3102800-3103000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr7:3102800-3103000	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr7:3102800-3103200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr7:3102800-3103200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr7:3103000-3103200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
44	chr7:3103000-3103200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
45	chr7:3103000-3107400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
46	chr7:3103200-3104400	Enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr7:3103200-3105200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr7:3103200-3106000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr7:3103200-3108600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
50	chr7:3103200-3110200	Enhancers	Primary T helper cells fromperipheralblood	blood

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