Variant report

Variant	esv2761100
Chromosome Location	chr7:102335787-102481978
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1644)
CpG islands
(count:1039)
Chromatin interactive
region (count:29)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1644 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102478846-102479241	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:102389084-102389458	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:102339769-102340073	K562	blood:	n/a	n/a
4	ARID3A	chr7:102452449-102452773	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:102386048-102386259	K562	blood:	n/a	n/a
6	ARID3A	chr7:102386072-102386189	HepG2	liver:	n/a	n/a
7	ATF1	chr7:102339824-102340183	K562	blood:	n/a	n/a
8	ATF1	chr7:102389031-102389497	K562	blood:	n/a	n/a
9	ATF2	chr7:102475368-102475893	GM12878	blood:	n/a	n/a
10	ATF2	chr7:102353714-102354151	GM12878	blood:	n/a	n/a
11	ATF2	chr7:102389081-102389544	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr7:102481620-102482163	GM12878	blood:	n/a	n/a
13	ATF2	chr7:102389108-102389584	GM12878	blood:	n/a	n/a
14	ATF2	chr7:102353660-102354116	GM12878	blood:	n/a	n/a
15	ATF2	chr7:102475399-102475848	GM12878	blood:	n/a	n/a
16	BATF	chr7:102352581-102352892	GM12878	blood:	n/a	n/a
17	BATF	chr7:102410945-102411178	GM12878	blood:	n/a	n/a
18	BATF	chr7:102355431-102355796	GM12878	blood:	n/a	n/a
19	BATF	chr7:102356182-102356563	GM12878	blood:	n/a	n/a
20	BATF	chr7:102400487-102400681	GM12878	blood:	n/a	n/a
21	BATF	chr7:102353721-102354553	GM12878	blood:	n/a	n/a
22	BATF	chr7:102353557-102354555	GM12878	blood:	n/a	n/a
23	BATF	chr7:102475444-102475777	GM12878	blood:	n/a	chr7:102475647-102475658 chr7:102475648-102475658
24	BATF	chr7:102356109-102356632	GM12878	blood:	n/a	n/a
25	BATF	chr7:102400501-102400644	GM12878	blood:	n/a	n/a
26	BATF	chr7:102481751-102482055	GM12878	blood:	n/a	n/a
27	BATF	chr7:102475426-102475852	GM12878	blood:	n/a	chr7:102475647-102475658 chr7:102475648-102475658
28	BATF	chr7:102352630-102352884	GM12878	blood:	n/a	n/a
29	BATF	chr7:102355536-102355847	GM12878	blood:	n/a	n/a
30	BATF	chr7:102382888-102383234	GM12878	blood:	n/a	n/a
31	BATF	chr7:102481731-102482084	GM12878	blood:	n/a	n/a
32	BCL11A	chr7:102352667-102352857	GM12878	blood:	n/a	n/a
33	BCL11A	chr7:102410971-102411150	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:102353677-102354018	GM12878	blood:	n/a	n/a
35	BCL11A	chr7:102353630-102354526	GM12878	blood:	n/a	n/a
36	BCL11A	chr7:102356071-102356558	GM12878	blood:	n/a	n/a
37	BCL11A	chr7:102475497-102475744	GM12878	blood:	n/a	n/a
38	BCL11A	chr7:102352587-102352904	GM12878	blood:	n/a	n/a
39	BCL11A	chr7:102475417-102475810	GM12878	blood:	n/a	n/a
40	BCL11A	chr7:102382918-102383177	GM12878	blood:	n/a	n/a
41	BCL11A	chr7:102355571-102355806	GM12878	blood:	n/a	n/a
42	BCL11A	chr7:102356208-102356576	GM12878	blood:	n/a	n/a
43	BCL11A	chr7:102481679-102482030	GM12878	blood:	n/a	n/a
44	BCL11A	chr7:102354099-102354536	GM12878	blood:	n/a	n/a
45	BCL3	chr7:102454575-102454898	GM12878	blood:	n/a	n/a
46	BCLAF1	chr7:102481611-102482122	GM12878	blood:	n/a	n/a
47	BCLAF1	chr7:102475385-102475792	GM12878	blood:	n/a	n/a
48	BCLAF1	chr7:102353659-102353980	GM12878	blood:	n/a	n/a
49	BHLHE40	chr7:102388971-102389373	HepG2	liver:	n/a	n/a
50	BHLHE40	chr7:102388850-102389527	K562	blood:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102389191-102389241	PrEC	prostate:	n/a
2	chr7:102389481-102389531	SKMC	muscle:	n/a
3	chr7:102389191-102389241	PrEC	prostate:	n/a
4	chr7:102389481-102389531	SKMC	muscle:	n/a
5	chr7:102389191-102389241	U87	brain:	n/a
6	chr7:102385712-102385762	GM19239	blood:	n/a
7	chr7:102388500-102388550	HMEC	breast:	n/a
8	chr7:102470281-102470331	AG09319	gingival:	n/a
9	chr7:102453328-102453378	PrEC	prostate:	n/a
10	chr7:102477205-102477255	HUVEC	blood vessel:	n/a
11	chr7:102389481-102389531	NHDF-neo	bronchial:	n/a
12	chr7:102389275-102389325	NHBE	bronchial:	n/a
13	chr7:102389481-102389531	HUVEC	blood vessel:	n/a
14	chr7:102389315-102389365	A549	lung:	n/a
15	chr7:102389892-102389942	HepG2	liver:	n/a
16	chr7:102470281-102470331	HepG2	liver:	n/a
17	chr7:102389205-102389255	HCT-116	colon:	n/a
18	chr7:102453328-102453378	HEK293	kidney:	embryo
19	chr7:102470281-102470331	AG10803	skin:	n/a
20	chr7:102390529-102390579	HCT-116	colon:	n/a
21	chr7:102385712-102385762	RPTEC	kidney:	n/a
22	chr7:102388500-102388550	SAEC	small airway:	n/a
23	chr7:102453328-102453378	NHDF-neo	bronchial:	n/a
24	chr7:102389205-102389255	HepG2	liver:	n/a
25	chr7:102389327-102389377	AG10803	skin:	n/a
26	chr7:102470281-102470331	GM12891	blood:	n/a
27	chr7:102389392-102389442	Hela-S3	cervix:	n/a
28	chr7:102389790-102389840	ProgFib	skin:	n/a
29	chr7:102390529-102390579	GM06990	blood:	n/a
30	chr7:102389481-102389531	NB4	blood:	n/a
31	chr7:102389327-102389377	NB4	blood:	n/a
32	chr7:102470281-102470331	HRE	kidney:	n/a
33	chr7:102449340-102449390	HCPEpiC	choroid plexus:	n/a
34	chr7:102389191-102389241	AG09309	skin:	n/a
35	chr7:102389327-102389377	ProgFib	skin:	n/a
36	chr7:102453328-102453378	SKMC	muscle:	n/a
37	chr7:102389191-102389241	HPAEpiC	pulmonary alveolar:	n/a
38	chr7:102389392-102389442	MCF-7	breast:	n/a
39	chr7:102389327-102389377	AG09309	skin:	n/a
40	chr7:102449340-102449390	NH-A	brain:	n/a
41	chr7:102470281-102470331	ovcar-3	ovarian:	n/a
42	chr7:102453328-102453378	SK-N-SH	brain:	n/a
43	chr7:102389481-102389531	HAEpiC	amniotic membrane:	n/a
44	chr7:102470281-102470331	HRCEpiC	kidney:	n/a
45	chr7:102388500-102388550	ECC-1	luminal epithelium:	n/a
46	chr7:102389790-102389840	GM12891	blood:	n/a
47	chr7:102477205-102477255	AG04449	skin:	fetal
48	chr7:102389790-102389840	ECC-1	luminal epithelium:	n/a
49	chr7:102388500-102388550	NHBE	bronchial:	n/a
50	chr7:102389392-102389442	H1-hESC	embryonic stem cell:	embryo

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:102471265..102473661-chr7:102474795..102476825,2	K562	blood:
2	chr7:102389047..102390959-chr7:102788572..102791008,2	K562	blood:
3	chr7:102446461..102450682-chr7:102452402..102456233,5	K562	blood:
4	chr7:102389494..102391981-chr7:102714130..102716680,2	MCF-7	breast:
5	chr7:102450714..102452892-chr7:102454122..102456841,2	K562	blood:
6	chr7:76751236..76752770-chr7:102389322..102390934,2	MCF-7	breast:
7	chr7:102458375..102460773-chr7:102462398..102464575,2	K562	blood:
8	chr7:102474929..102477472-chr7:102495351..102498066,2	K562	blood:
9	chr7:102466773..102468562-chr7:102472761..102475356,2	MCF-7	breast:
10	chr7:102446461..102450682-chr7:102452402..102456233,5	K562	blood:
11	chr7:102459530..102461153-chr7:102484743..102487140,2	K562	blood:
12	chr7:102388357..102390801-chr7:102713734..102717426,3	K562	blood:
13	chr7:102387955..102390990-chr7:102714406..102717094,4	MCF-7	breast:
14	chr7:102430529..102431497-chr7:102702527..102703245,2	K562	blood:
15	chr7:102459925..102462268-chr7:102466191..102467871,2	K562	blood:
16	chr7:102396782..102398459-chr7:102714684..102716364,2	MCF-7	breast:
17	chr7:102473090..102475084-chr7:102477070..102479073,2	K562	blood:
18	chr7:76751236..76751872-chr7:102389110..102389768,2	MCF-7	breast:
19	chr7:102470809..102472496-chr7:102473289..102475572,2	MCF-7	breast:
20	chr7:102449182..102452214-chr7:102453198..102455672,3	K562	blood:
21	chr7:102445308..102447740-chr7:102490751..102492572,2	K562	blood:
22	chr7:102452440..102454909-chr7:102615064..102617723,2	K562	blood:
23	chr7:102473443..102475589-chr7:102480022..102482918,2	K562	blood:
24	chr7:102462907..102465712-chr7:102475017..102477373,2	K562	blood:
25	chr7:102451931..102453738-chr7:102614138..102615717,2	K562	blood:
26	chr7:76750772..76751740-chr7:102389401..102390157,2	HCT-116	colon:
27	chr7:102459925..102462268-chr7:102466191..102467871,2	K562	blood:
28	chr7:102458375..102460773-chr7:102462398..102464575,2	K562	blood:
29	chr7:102449182..102452214-chr7:102453198..102455672,3	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC105052.1-2	chr7:102456637-102456718	NONHSAT122523
2	lnc-AC105052.1-2	chr7:102453685-102453978	NONHSAT122523
3	lnc-AC105052.1-2	chr7:102454781-102454863	NONHSAT122523

No data

Variant related genes	Relation type
RNU6-1136P	TF binding region
ENSG00000213385	TF binding region
FBXL13	TF binding region
RASA4DP	TF binding region
FAM185A	TF binding region
RNU6-1136P	CpG island
ENSG00000213385	CpG island
FBXL13	CpG island
RASA4DP	CpG island
FAM185A	CpG island
ENSG00000252643	chromatin interactions
ENSG00000161048	chromatin interactions
ENSG00000214439	chromatin interactions
ENSG00000170632	chromatin interactions
ENSG00000135205	chromatin interactions
ENSG00000161040	chromatin interactions
ENSG00000238324	chromatin interactions

Extended variants
information (count: 3649 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:3649 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532829404	chr7:102335803-102335804	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs543961723	chr7:102335851-102335852	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs564832087	chr7:102335852-102335853	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs57336315	chr7:102335942-102335943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs547166095	chr7:102336106-102336107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs565382772	chr7:102336111-102336112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs75518823	chr7:102336124-102336125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147119926	chr7:102336130-102336131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs569578026	chr7:102336214-102336215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs536870775	chr7:102336230-102336231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs558674184	chr7:102336305-102336306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571662101	chr7:102336306-102336307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188805862	chr7:102336307-102336308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148131283	chr7:102336313-102336314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs76793111	chr7:102336800-102336801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs77589550	chr7:102336806-102336807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs75571789	chr7:102336807-102336808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs75762802	chr7:102336811-102336812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs78970248	chr7:102336815-102336816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs570675591	chr7:102336821-102336822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534497580	chr7:102336822-102336823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554342468	chr7:102336830-102336831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs75277484	chr7:102336835-102336836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs76388256	chr7:102336840-102336841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs79388995	chr7:102336847-102336848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs77561268	chr7:102336848-102336849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs77757364	chr7:102336851-102336852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs536668147	chr7:102336860-102336861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs76183729	chr7:102336869-102336870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs74397447	chr7:102336871-102336872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs80106885	chr7:102336878-102336879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs79567476	chr7:102336879-102336880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs76791224	chr7:102336889-102336890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs76926811	chr7:102336890-102336891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs80011661	chr7:102336905-102336906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs76802229	chr7:102336908-102336909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs76729196	chr7:102336942-102336943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs75990271	chr7:102336979-102336980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576348293	chr7:102337042-102337043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs77305351	chr7:102337056-102337057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs558963690	chr7:102337057-102337058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577397956	chr7:102337111-102337112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186237237	chr7:102337147-102337148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs145922783	chr7:102337184-102337185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs574145940	chr7:102337200-102337201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs139823589	chr7:102337228-102337229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs563339051	chr7:102337317-102337318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs375211897	chr7:102337323-102337324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs73404364	chr7:102337347-102337348	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs191884684	chr7:102337352-102337353	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	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
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD

Chromatin state (count:1528 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102335200-102336400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr7:102335200-102336400	Enhancers	Primary B cells from peripheral blood	blood
3	chr7:102335200-102336400	Enhancers	GM12878-XiMat	blood
4	chr7:102336000-102336400	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr7:102336800-102337400	Enhancers	K562	blood
6	chr7:102337400-102339400	Weak transcription	K562	blood
7	chr7:102338200-102339600	Enhancers	Hela-S3	cervix
8	chr7:102338600-102339800	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr7:102339400-102339600	Enhancers	K562	blood
10	chr7:102339600-102339800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr7:102339600-102340000	Flanking Active TSS	Hela-S3	cervix
12	chr7:102339600-102340400	Flanking Active TSS	K562	blood
13	chr7:102339800-102340600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr7:102340000-102340200	Enhancers	Hela-S3	cervix
15	chr7:102340400-102341600	Enhancers	K562	blood
16	chr7:102351800-102352800	Enhancers	GM12878-XiMat	blood
17	chr7:102352800-102353200	Weak transcription	GM12878-XiMat	blood
18	chr7:102353200-102353400	Enhancers	GM12878-XiMat	blood
19	chr7:102353400-102353600	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr7:102353400-102353800	Active TSS	Primary neutrophils fromperipheralblood	blood
21	chr7:102353400-102354000	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr7:102353400-102354000	Enhancers	Primary T cells fromperipheralblood	blood
23	chr7:102353400-102354000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
24	chr7:102353400-102354000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr7:102353400-102354200	Enhancers	A549	lung
26	chr7:102353400-102354200	Flanking Active TSS	GM12878-XiMat	blood
27	chr7:102353400-102355000	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr7:102353400-102355200	Enhancers	HMEC	breast
29	chr7:102353400-102356600	Enhancers	NHEK	skin
30	chr7:102353600-102353800	Enhancers	NH-A	brain
31	chr7:102353600-102354000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr7:102353600-102354000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr7:102353600-102354000	Enhancers	Primary B cells from peripheral blood	blood
34	chr7:102353600-102354000	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr7:102353600-102354000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
36	chr7:102353600-102354000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr7:102353600-102354000	Enhancers	Gastric	stomach
38	chr7:102353600-102354200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr7:102353600-102354200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr7:102353600-102354200	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr7:102353600-102354200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
42	chr7:102353600-102354200	Enhancers	Primary T killer memory cells from peripheral blood	blood
43	chr7:102353600-102354200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr7:102353600-102354200	Enhancers	Hela-S3	cervix
45	chr7:102353600-102354200	Enhancers	HSMMtube	muscle
46	chr7:102353600-102354200	Bivalent Enhancer	HUVEC	blood vessel
47	chr7:102353600-102354200	Enhancers	K562	blood
48	chr7:102353600-102354200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr7:102353600-102354200	Enhancers	NHLF	lung
50	chr7:102353600-102354800	Enhancers	Osteobl	bone

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