Variant report

Variant	esv3380438
Chromosome Location	chr7:100176116-100180514
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:67)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:67 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr7:100177074-100177274	K562	blood:	n/a	n/a
2	CHD2	chr7:100176622-100176822	HepG2	liver:	n/a	n/a
3	CTCF	chr7:100178392-100178492	GM19239	blood:	n/a	n/a
4	CUX1	chr7:100177898-100177910	K562	blood:	n/a	n/a
5	EP300	chr7:100179834-100180232	T-47D	breast:	n/a	n/a
6	GATA3	chr7:100179672-100180493	MCF-7	breast:	n/a	n/a
7	HDAC2	chr7:100179696-100180522	MCF-7	breast:	n/a	n/a
8	MAX	chr7:100179541-100180502	MCF-7	breast:	n/a	n/a
9	MAX	chr7:100179502-100180360	MCF-7	breast:	n/a	n/a
10	MAX	chr7:100178391-100178569	NB4	blood:	n/a	chr7:100178457-100178467
11	MYC	chr7:100179869-100179987	MCF-7	breast:	n/a	n/a
12	MYC	chr7:100178439-100178475	HUVEC	blood vessel:	n/a	chr7:100178457-100178467
13	MYC	chr7:100179869-100179971	MCF-7	breast:	n/a	n/a
14	MYC	chr7:100179774-100180083	MCF-7	breast:	n/a	n/a
15	NR2C2	chr7:100178204-100178637	GM12878	blood:	n/a	n/a
16	NR2F2	chr7:100179530-100180731	MCF-7	breast:	n/a	n/a
17	NR2F2	chr7:100179593-100180522	MCF-7	breast:	n/a	n/a
18	POLR2A	chr7:100176280-100176710	GM12891	blood:	n/a	n/a
19	POLR2A	chr7:100177892-100178817	HepG2	liver:	n/a	n/a
20	POLR2A	chr7:100177981-100178629	GM12878	blood:	n/a	n/a
21	POLR2A	chr7:100177958-100178772	K562	blood:	n/a	n/a
22	POLR2A	chr7:100176121-100176393	GM12878	blood:	n/a	n/a
23	POLR2A	chr7:100176361-100176934	GM12878	blood:	n/a	n/a
24	POLR2A	chr7:100178240-100178507	HepG2	liver:	n/a	n/a
25	POLR2A	chr7:100176060-100176875	GM12892	blood:	n/a	n/a
26	POLR2A	chr7:100175332-100177004	K562	blood:	n/a	n/a
27	POLR2A	chr7:100163833-100176987	HepG2	liver:	n/a	n/a
28	POLR2A	chr7:100177235-100180963	HepG2	liver:	n/a	n/a
29	POLR2A	chr7:100175049-100176951	GM12878	blood:	n/a	n/a
30	POLR2A	chr7:100176258-100177000	GM12891	blood:	n/a	n/a
31	POLR2A	chr7:100177185-100177965	K562	blood:	n/a	n/a
32	POLR2A	chr7:100177875-100177889	HepG2	liver:	n/a	n/a
33	POLR2A	chr7:100177958-100178693	PANC-1	pancreas:	n/a	n/a
34	POLR2A	chr7:100178357-100178727	GM12878	blood:	n/a	n/a
35	POLR2A	chr7:100179200-100179302	K562	blood:	n/a	n/a
36	POLR2A	chr7:100178130-100178643	GM12891	blood:	n/a	n/a
37	POLR2A	chr7:100176358-100176562	GM12878	blood:	n/a	n/a
38	POLR2A	chr7:100176370-100176709	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr7:100179784-100180383	K562	blood:	n/a	n/a
40	POLR2A	chr7:100176064-100176345	GM12878	blood:	n/a	n/a
41	POLR2A	chr7:100175062-100176864	HL-60	blood:	n/a	n/a
42	POLR2A	chr7:100176621-100176953	GM12878	blood:	n/a	n/a
43	POLR2A	chr7:100176198-100176788	K562	blood:	n/a	n/a
44	POLR2A	chr7:100178327-100178502	HUVEC	blood vessel:	n/a	n/a
45	POLR2A	chr7:100177335-100177910	K562	blood:	n/a	n/a
46	POLR2A	chr7:100178259-100178673	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr7:100178082-100178570	K562	blood:	n/a	n/a
48	POLR2A	chr7:100177201-100179008	GM12878	blood:	n/a	n/a
49	POLR2A	chr7:100179103-100179656	K562	blood:	n/a	n/a
50	POLR2A	chr7:100175978-100176883	GM12892	blood:	n/a	n/a

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:100180263..100184567-chr7:100269497..100273047,5	K562	blood:
2	chr7:100178369..100186125-chr7:100269651..100278553,26	MCF-7	breast:
3	chr7:100070743..100075629-chr7:100178965..100183270,7	K562	blood:
4	chr7:100180512..100183004-chr7:100452297..100454557,2	MCF-7	breast:
5	chr7:100076419..100078761-chr7:100175635..100177478,2	K562	blood:
6	chr7:100179244..100181643-chr7:100480633..100482895,2	MCF-7	breast:
7	chr7:100031924..100034212-chr7:100179842..100183716,3	MCF-7	breast:
8	chr7:100059236..100061028-chr7:100176403..100178856,2	K562	blood:
9	chr7:100179326..100185857-chr7:100269460..100275597,19	MCF-7	breast:
10	chr7:100176059..100178977-chr7:100238614..100240388,2	K562	blood:
11	chr7:100179385..100182357-chr7:100273234..100275046,2	K562	blood:

No data

Variant related genes	Relation type
LRCH4	TF binding region
FBXO24	TF binding region
SAP25	TF binding region
ENSG00000160813	chromatin interactions
ENSG00000240211	chromatin interactions
ENSG00000172354	chromatin interactions
ENSG00000087087	chromatin interactions
ENSG00000146828	chromatin interactions
ENSG00000241357	chromatin interactions
ENSG00000166925	chromatin interactions
ENSG00000106327	chromatin interactions
ENSG00000264758	chromatin interactions

Extended variants
information (count: 243 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:243 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199661269	chr7:100176136-100176137	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs370226693	chr7:100176142-100176143	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs546248076	chr7:100176154-100176155	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs201238982	chr7:100176172-100176173	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs115205235	chr7:100176185-100176186	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs377423695	chr7:100176248-100176249	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs371175219	chr7:100176266-100176267	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs375534637	chr7:100176298-100176299	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs368249205	chr7:100176302-100176303	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs372575327	chr7:100176334-100176335	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs52833865	chr7:100176362-100176363	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs373972496	chr7:100176363-100176364	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs539637465	chr7:100176385-100176386	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs551961361	chr7:100176386-100176387	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs368111306	chr7:100176394-100176395	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs183189535	chr7:100176395-100176396	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs146938731	chr7:100176398-100176399	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs535627175	chr7:100176401-100176402	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs371264894	chr7:100176411-100176412	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs534322621	chr7:100176462-100176463	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs555443752	chr7:100176511-100176512	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs188664354	chr7:100176569-100176570	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs538272964	chr7:100176602-100176603	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs145602923	chr7:100176630-100176631	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs575618217	chr7:100176631-100176632	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs545631080	chr7:100176658-100176659	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs564324518	chr7:100176660-100176661	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs548032509	chr7:100176665-100176666	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs193017515	chr7:100176676-100176677	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs540307690	chr7:100176725-100176726	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs561474156	chr7:100176819-100176820	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs574181583	chr7:100176829-100176830	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs543844463	chr7:100176831-100176832	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs562802515	chr7:100176838-100176839	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs138023624	chr7:100176875-100176876	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs551655963	chr7:100176918-100176919	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs567070506	chr7:100176943-100176944	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs527917438	chr7:100176944-100176945	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs549437959	chr7:100176948-100176949	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs567808867	chr7:100176949-100176950	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs113571843	chr7:100176985-100176986	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
42	rs185744207	chr7:100176987-100176988	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs540170164	chr7:100176991-100176992	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs187506095	chr7:100176992-100176993	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs113870818	chr7:100177044-100177045	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
46	rs557799357	chr7:100177081-100177082	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs544777793	chr7:100177092-100177093	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs191390486	chr7:100177136-100177137	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs540101709	chr7:100177137-100177138	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs555033930	chr7:100177169-100177170	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	21865298	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:351 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100168000-100179800	Weak transcription	Right Atrium	heart
2	chr7:100168200-100177600	Weak transcription	HMEC	breast
3	chr7:100168600-100179600	Strong transcription	NHLF	lung
4	chr7:100168800-100177400	Weak transcription	NHDF-Ad	bronchial
5	chr7:100169400-100178200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr7:100169400-100178400	Strong transcription	Primary neutrophils fromperipheralblood	blood
7	chr7:100169600-100176200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr7:100169600-100178600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr7:100169600-100179000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr7:100169600-100180000	Strong transcription	Fetal Intestine Small	intestine
11	chr7:100169600-100180200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr7:100169800-100176200	Weak transcription	A549	lung
13	chr7:100169800-100177200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:100169800-100178200	Weak transcription	Fetal Heart	heart
15	chr7:100169800-100179400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
16	chr7:100169800-100180000	Strong transcription	Thymus	Thymus
17	chr7:100170000-100177600	Weak transcription	Fetal Kidney	kidney
18	chr7:100170000-100178200	Strong transcription	Primary T helper cells fromperipheralblood	blood
19	chr7:100170000-100181200	Weak transcription	Hela-S3	cervix
20	chr7:100170200-100177400	Strong transcription	Primary T helper cells PMA-I stimulated	--
21	chr7:100170200-100178000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr7:100170200-100178600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr7:100170200-100180200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr7:100170200-100180200	Strong transcription	Sigmoid Colon	Sigmoid Colon
25	chr7:100170200-100180800	Strong transcription	Brain Germinal Matrix	brain
26	chr7:100170400-100177800	Weak transcription	NH-A	brain
27	chr7:100170400-100179400	Strong transcription	Esophagus	oesophagus
28	chr7:100170400-100179600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr7:100170400-100179800	Strong transcription	Primary monocytes fromperipheralblood	blood
30	chr7:100170400-100180200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr7:100170600-100177800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr7:100170600-100178800	Strong transcription	Colonic Mucosa	Colon
33	chr7:100170600-100179200	Strong transcription	Dnd41	blood
34	chr7:100170600-100179600	Strong transcription	Fetal Thymus	thymus
35	chr7:100170600-100180800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr7:100170800-100178400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr7:100170800-100178600	Strong transcription	Primary B cells from peripheral blood	blood
38	chr7:100170800-100179400	Strong transcription	Gastric	stomach
39	chr7:100170800-100179800	Strong transcription	Fetal Muscle Leg	muscle
40	chr7:100170800-100179800	Strong transcription	Monocytes-CD14+_RO01746	blood
41	chr7:100171000-100177400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr7:100171000-100178200	Strong transcription	Pancreas	Pancrea
43	chr7:100171000-100179600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr7:100171000-100179800	Strong transcription	Adipose Nuclei	Adipose
45	chr7:100171000-100180200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr7:100171000-100180600	Strong transcription	Muscle Satellite Cultured Cells	--
47	chr7:100171200-100177400	Weak transcription	HepG2	liver
48	chr7:100171200-100178200	Strong transcription	Primary T cells from cord blood	blood
49	chr7:100171200-100179800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr7:100171400-100176200	Strong transcription	Right Ventricle	heart

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