Variant report

Variant	esv1824630
Chromosome Location	chr7:99614770-99639445
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:75)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:99615508..99617156-chr7:99618905..99620431,2	MCF-7	breast:
2	chr7:99633170..99637307-chr7:99685245..99688799,3	K562	blood:
3	chr7:99634660..99636728-chr7:99636829..99638955,3	MCF-7	breast:
4	chr7:99613052..99614661-chr7:99625234..99626812,2	MCF-7	breast:
5	chr7:99619042..99622957-chr7:99630011..99632854,4	MCF-7	breast:
6	chr7:99603071..99604678-chr7:99629876..99631429,2	MCF-7	breast:
7	chr7:99519344..99522278-chr7:99625729..99627804,2	K562	blood:
8	chr7:99617125..99619542-chr7:99633323..99635330,2	K562	blood:
9	chr7:99626508..99630728-chr7:99630857..99634217,6	MCF-7	breast:
10	chr7:99618852..99620390-chr7:99647489..99649484,2	MCF-7	breast:
11	chr7:99624486..99627047-chr7:99678745..99680467,2	K562	blood:
12	chr7:99589288..99591810-chr7:99612834..99614804,4	MCF-7	breast:
13	chr7:99620109..99621730-chr7:99637270..99638942,2	MCF-7	breast:
14	chr7:99618314..99620224-chr7:99678750..99680788,2	MCF-7	breast:
15	chr7:99618848..99621935-chr7:99625446..99628535,4	MCF-7	breast:
16	chr7:99590547..99592612-chr7:99626360..99629032,2	K562	blood:
17	chr7:99611956..99613934-chr7:99634714..99636555,2	K562	blood:
18	chr7:99626985..99629362-chr7:99630323..99632638,2	MCF-7	breast:
19	chr7:99635895..99638032-chr7:99640487..99642322,2	MCF-7	breast:
20	chr7:99623016..99624978-chr7:99629565..99632426,3	K562	blood:
21	chr7:99626222..99628459-chr7:99637263..99639191,3	MCF-7	breast:
22	chr7:99611578..99613517-chr7:99631513..99633210,2	K562	blood:
23	chr7:99618848..99621935-chr7:99625446..99628535,4	MCF-7	breast:
24	chr7:99615985..99617689-chr7:99629896..99631894,2	MCF-7	breast:
25	chr7:99615985..99617689-chr7:99629896..99631894,2	MCF-7	breast:
26	chr7:99588806..99591548-chr7:99620634..99622161,2	MCF-7	breast:
27	chr7:99614250..99615860-chr7:99701481..99703800,2	K562	blood:
28	chr7:99627608..99629341-chr7:99632124..99633750,2	K562	blood:
29	chr7:99631794..99640933-chr7:99644912..99651639,12	K562	blood:
30	chr7:99615508..99617156-chr7:99618905..99620431,2	MCF-7	breast:
31	chr7:99617125..99619542-chr7:99633323..99635330,2	K562	blood:
32	chr7:99613306..99615407-chr7:99637728..99640731,3	MCF-7	breast:
33	chr7:99612275..99615910-chr7:99677885..99681193,8	K562	blood:
34	chr7:99594172..99596915-chr7:99619216..99620782,2	K562	blood:
35	chr7:99619042..99622957-chr7:99630011..99632854,4	MCF-7	breast:
36	chr7:99611884..99615327-chr7:99716112..99720187,5	K562	blood:
37	chr7:99621050..99622719-chr7:99664810..99666515,2	MCF-7	breast:
38	chr7:99611831..99614044-chr7:99638316..99640846,2	K562	blood:
39	chr7:99611430..99615857-chr7:99675156..99681193,15	K562	blood:
40	chr7:99634660..99636728-chr7:99636829..99638955,3	MCF-7	breast:
41	chr7:99630304..99632812-chr7:99647212..99649132,2	MCF-7	breast:
42	chr7:99620109..99621730-chr7:99637270..99638942,2	MCF-7	breast:
43	chr7:99626167..99629081-chr7:99640250..99642340,2	K562	blood:
44	chr7:99613224..99616757-chr7:99646903..99650456,6	K562	blood:
45	chr7:99612131..99615242-chr7:99723277..99726662,3	K562	blood:
46	chr7:99515716..99518824-chr7:99610446..99615072,4	K562	blood:
47	chr7:99621923..99624506-chr7:99677011..99679788,2	K562	blood:
48	chr7:99629435..99632327-chr7:99685229..99688154,2	K562	blood:
49	chr7:99626268..99629732-chr7:99646321..99649999,3	MCF-7	breast:
50	chr7:99516539..99518815-chr7:99613011..99615072,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZSCAN21-2	chr7:99637173-99639311	NONHSAT122291

No data

Variant related genes	Relation type
ENSG00000168090	chromatin interactions
ENSG00000166508	chromatin interactions
ENSG00000221838	chromatin interactions
ENSG00000166997	chromatin interactions
ENSG00000166529	chromatin interactions
ENSG00000235713	chromatin interactions
ENSG00000166526	chromatin interactions
ENSG00000146833	chromatin interactions
ENSG00000242798	chromatin interactions
ENSG00000214309	chromatin interactions
ENSG00000106290	chromatin interactions
ENSG00000106261	chromatin interactions

Extended variants
information (count: 942 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:942 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35414630	chr7:99614770-99614771	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs370608091	chr7:99614779-99614780	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
3	rs111667828	chr7:99614780-99614781	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
4	rs545197295	chr7:99614781-99614782	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
5	rs143221456	chr7:99614804-99614805	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
6	rs199676744	chr7:99614841-99614842	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
7	rs560043050	chr7:99614850-99614851	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
8	rs4727444	chr7:99614851-99614852	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs182693512	chr7:99614871-99614872	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
10	rs188267664	chr7:99614896-99614897	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
11	rs531363379	chr7:99614933-99614934	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs549777653	chr7:99614936-99614937	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
13	rs144822538	chr7:99614944-99614945	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs538317172	chr7:99614964-99614965	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs547976187	chr7:99614970-99614971	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
16	rs370226796	chr7:99615070-99615071	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Genic enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
17	rs193172912	chr7:99615085-99615086	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs528530892	chr7:99615121-99615122	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs183815460	chr7:99615255-99615256	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs35531253	chr7:99615261-99615262	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs569984713	chr7:99615311-99615312	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs537062776	chr7:99615365-99615366	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs138664804	chr7:99615390-99615391	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs140316566	chr7:99615501-99615502	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs189176490	chr7:99615633-99615634	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs145568927	chr7:99615660-99615661	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs572181196	chr7:99615684-99615685	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs372459555	chr7:99615703-99615704	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs148051100	chr7:99615726-99615727	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs531603708	chr7:99615810-99615811	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs113962293	chr7:99615856-99615857	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs543453116	chr7:99615869-99615870	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs565411127	chr7:99615882-99615883	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs564681737	chr7:99615896-99615897	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs191279234	chr7:99615918-99615919	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs533469070	chr7:99615952-99615953	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs13228844	chr7:99615962-99615963	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs530250667	chr7:99615966-99615967	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs550736729	chr7:99615968-99615969	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs141850493	chr7:99615977-99615978	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs62484981	chr7:99616027-99616028	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs569126747	chr7:99616058-99616059	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs570022400	chr7:99616112-99616113	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs537300534	chr7:99616156-99616157	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs536510611	chr7:99616157-99616158	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs559199165	chr7:99616196-99616197	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs150608864	chr7:99616201-99616202	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs183756513	chr7:99616232-99616233	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs188186590	chr7:99616279-99616280	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs13243708	chr7:99616291-99616292	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance

Variant related diseases (count:95)

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
Stenocardia	21860640	CNVD
Vasospasm	21860640	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
Acute lymphoblastic leukemia	21339820	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
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1185 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99612800-99614800	Active TSS	iPS-20b Cell Line	embryonic stem cell
2	chr7:99612800-99615200	Active TSS	HUES64 Cell Line	embryonic stem cell
3	chr7:99613000-99614800	Active TSS	H1 Cell Line	embryonic stem cell
4	chr7:99613000-99615000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:99613000-99615000	Active TSS	Brain Cingulate Gyrus	brain
6	chr7:99613000-99615000	Active TSS	Brain Inferior Temporal Lobe	brain
7	chr7:99613000-99615000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
8	chr7:99613000-99615200	Active TSS	HSMMtube	muscle
9	chr7:99613000-99616600	Active TSS	Pancreatic Islets	Pancreatic Islet
10	chr7:99613200-99614800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr7:99613200-99615000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr7:99613200-99615000	Active TSS	Fetal Intestine Large	intestine
13	chr7:99613800-99614800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
14	chr7:99613800-99614800	Flanking Active TSS	Adipose Nuclei	Adipose
15	chr7:99613800-99614800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
16	chr7:99613800-99614800	Flanking Active TSS	Stomach Smooth Muscle	stomach
17	chr7:99613800-99614800	Flanking Active TSS	NH-A	brain
18	chr7:99613800-99615000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr7:99613800-99615000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr7:99613800-99615000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr7:99613800-99615200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr7:99613800-99615600	Transcr. at gene 5' and 3'	Dnd41	blood
23	chr7:99614000-99614800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
24	chr7:99614000-99614800	Flanking Active TSS	Duodenum Mucosa	Duodenum
25	chr7:99614000-99614800	Flanking Active TSS	Fetal Lung	lung
26	chr7:99614000-99614800	Flanking Active TSS	Rectal Smooth Muscle	rectum
27	chr7:99614000-99614800	Flanking Active TSS	HUVEC	blood vessel
28	chr7:99614000-99614800	Flanking Active TSS	Osteobl	bone
29	chr7:99614000-99615200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr7:99614000-99615600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr7:99614000-99615600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
32	chr7:99614000-99616400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr7:99614200-99614800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
34	chr7:99614200-99614800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr7:99614200-99614800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr7:99614200-99614800	Enhancers	Primary B cells from peripheral blood	blood
37	chr7:99614200-99614800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
38	chr7:99614200-99614800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
39	chr7:99614200-99614800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
40	chr7:99614200-99614800	Flanking Active TSS	Colon Smooth Muscle	Colon
41	chr7:99614200-99614800	Flanking Active TSS	Fetal Stomach	stomach
42	chr7:99614200-99614800	Flanking Active TSS	K562	blood
43	chr7:99614200-99614800	Flanking Active TSS	NHEK	skin
44	chr7:99614200-99615000	Flanking Active TSS	Fetal Brain Female	brain
45	chr7:99614200-99615200	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr7:99614200-99615200	Enhancers	Primary T cells fromperipheralblood	blood
47	chr7:99614200-99615200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr7:99614200-99615400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr7:99614200-99615400	Flanking Active TSS	Brain Anterior Caudate	brain
50	chr7:99614200-99615600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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