Variant report

Variant	esv1801863
Chromosome Location	chr7:104699637-104713419
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:115)
CpG islands
(count:0)
Chromatin interactive
region (count:37)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:115 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:104701861-104701905	K562	blood:	n/a	n/a
2	BRCA1	chr7:104699797-104699927	GM12878	blood:	n/a	n/a
3	CCNT2	chr7:104704291-104704348	K562	blood:	n/a	n/a
4	CEBPB	chr7:104709975-104710268	A549	lung:	n/a	chr7:104710093-104710104 chr7:104710154-104710165
5	CEBPB	chr7:104713326-104713386	K562	blood:	n/a	n/a
6	CEBPB	chr7:104709931-104710272	K562	blood:	n/a	chr7:104710093-104710104 chr7:104710154-104710165
7	CEBPB	chr7:104709981-104710271	HepG2	liver:	n/a	chr7:104710093-104710104 chr7:104710154-104710165
8	CTCF	chr7:104708303-104708350	Fibrobl	skin:	n/a	n/a
9	CTCF	chr7:104708978-104709019	A549	lung:	n/a	n/a
10	CTCF	chr7:104709320-104709470	MCF-7	breast:	n/a	n/a
11	CTCF	chr7:104711913-104711929	MCF-7	breast:	n/a	n/a
12	CTCF	chr7:104709380-104709530	BE2_C	brain:	n/a	n/a
13	CUX1	chr7:104704837-104704966	K562	blood:	n/a	n/a
14	GATA1	chr7:104708973-104709816	PBDE	blood:	n/a	n/a
15	IRF1	chr7:104702054-104702252	K562	blood:	n/a	chr7:104702118-104702125
16	IRF1	chr7:104705571-104705642	K562	blood:	n/a	n/a
17	JUN	chr7:104699688-104699935	K562	blood:	n/a	n/a
18	JUND	chr7:104710263-104710481	HepG2	liver:	n/a	n/a
19	MAFK	chr7:104701423-104701684	IMR90	lung:	n/a	n/a
20	MAZ	chr7:104701775-104701890	HepG2	liver:	n/a	n/a
21	MYC	chr7:104711926-104711928	MCF-7	breast:	n/a	n/a
22	MYC	chr7:104708958-104709054	MCF-7	breast:	n/a	n/a
23	MYC	chr7:104711871-104711959	MCF-7	breast:	n/a	n/a
24	MYC	chr7:104711905-104711951	MCF10A-Er-Src	breast:	n/a	n/a
25	MYC	chr7:104711888-104711994	MCF-7	breast:	n/a	n/a
26	NFYB	chr7:104700727-104700780	Hela-S3	cervix:	n/a	n/a
27	NRF1	chr7:104699841-104699922	GM12878	blood:	n/a	n/a
28	PBX3	chr7:104708944-104709114	GM12878	blood:	n/a	n/a
29	POLR2A	chr7:104700968-104701082	HepG2	liver:	n/a	n/a
30	POLR2A	chr7:104708098-104708538	GM12878	blood:	n/a	n/a
31	POLR2A	chr7:104708965-104709276	GM12878	blood:	n/a	n/a
32	POLR2A	chr7:104708228-104708338	ProgFib	skin:	n/a	n/a
33	POLR2A	chr7:104707613-104708887	K562	blood:	n/a	n/a
34	POLR2A	chr7:104701315-104701327	MCF-7	breast:	n/a	n/a
35	POLR2A	chr7:104701188-104701313	MCF-7	breast:	n/a	n/a
36	POLR2A	chr7:104711841-104712068	MCF-7	breast:	n/a	n/a
37	POLR2A	chr7:104711892-104712002	K562	blood:	n/a	n/a
38	POLR2A	chr7:104708244-104708422	MCF-7	breast:	n/a	n/a
39	POLR2A	chr7:104705547-104705575	GM12878	blood:	n/a	n/a
40	POLR2A	chr7:104712170-104712374	MCF-7	breast:	n/a	n/a
41	POLR2A	chr7:104700480-104700570	MCF-7	breast:	n/a	n/a
42	POLR2A	chr7:104709046-104709245	GM12878	blood:	n/a	n/a
43	POLR2A	chr7:104708185-104708419	MCF-7	breast:	n/a	n/a
44	POLR2A	chr7:104713011-104713170	HepG2	liver:	n/a	n/a
45	POLR2A	chr7:104704177-104704285	MCF-7	breast:	n/a	n/a
46	POLR2A	chr7:104700712-104700800	MCF-7	breast:	n/a	n/a
47	POLR2A	chr7:104708210-104708345	HepG2	liver:	n/a	n/a
48	POLR2A	chr7:104712089-104712097	MCF-7	breast:	n/a	n/a
49	POLR2A	chr7:104704921-104704993	HUVEC	blood vessel:	n/a	n/a
50	POLR2A	chr7:104710139-104710270	HepG2	liver:	n/a	n/a

No data

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:104702912..104705436-chr7:104706409..104709574,3	K562	blood:
2	chr7:104651595..104655365-chr7:104705718..104710034,4	MCF-7	breast:
3	chr7:104692480..104694895-chr7:104700465..104702158,2	MCF-7	breast:
4	chr7:104707915..104710491-chr7:104712651..104715318,2	MCF-7	breast:
5	chr7:104709756..104711654-chr7:104713737..104716023,2	MCF-7	breast:
6	chr7:104625024..104626547-chr7:104710166..104712101,2	MCF-7	breast:
7	chr7:104707915..104710491-chr7:104712651..104715318,2	MCF-7	breast:
8	chr12:90515370..90515898-chr7:104705136..104706082,2	MCF-7	breast:
9	chr7:104652104..104656031-chr7:104693551..104701213,11	MCF-7	breast:
10	chr7:104702912..104705436-chr7:104706409..104709574,3	K562	blood:
11	chr7:104689941..104692493-chr7:104702992..104705464,2	MCF-7	breast:
12	chr7:104666087..104669170-chr7:104700270..104702225,3	K562	blood:
13	chr7:104699830..104702178-chr7:104704805..104707713,3	K562	blood:
14	chr7:104706055..104708042-chr7:104708063..104710703,2	K562	blood:
15	chr7:104650546..104656206-chr7:104695535..104706992,23	K562	blood:
16	chr7:104650794..104654055-chr7:104707795..104709851,3	K562	blood:
17	chr7:104649023..104655837-chr7:104707951..104714558,12	K562	blood:
18	chr7:104623725..104625660-chr7:104712906..104715698,2	K562	blood:
19	chr7:104652687..104654984-chr7:104712550..104718501,6	MCF-7	breast:
20	chr7:104707718..104709440-chr7:104709810..104711789,2	MCF-7	breast:
21	chr7:104699830..104702178-chr7:104704805..104707713,3	K562	blood:
22	chr7:104649592..104657753-chr7:104694428..104703365,16	MCF-7	breast:
23	chr7:104619886..104621956-chr7:104705400..104707760,2	K562	blood:
24	chr7:104651636..104654670-chr7:104701757..104705518,5	MCF-7	breast:
25	chr7:104706055..104708042-chr7:104708063..104710703,2	K562	blood:
26	chr7:104658414..104660571-chr7:104698662..104700475,2	K562	blood:
27	chr7:104647386..104649426-chr7:104699731..104702282,2	K562	blood:
28	chr7:104647926..104656528-chr7:104691112..104706949,31	K562	blood:
29	chr7:104707718..104709440-chr7:104709810..104711789,2	MCF-7	breast:
30	chr7:104705262..104706850-chr7:104711768..104713879,2	K562	blood:
31	chr7:104712455..104714746-chr7:104716904..104718437,2	K562	blood:
32	chr7:104652258..104656223-chr7:104710394..104715807,8	K562	blood:
33	chr7:104693711..104695531-chr7:104698360..104700318,2	MCF-7	breast:
34	chr7:104705262..104706850-chr7:104711768..104713879,2	K562	blood:
35	chr7:104621807..104625592-chr7:104704805..104708118,3	K562	blood:
36	chr7:104705262..104710596-chr7:104710916..104715928,6	K562	blood:
37	chr7:104705262..104710596-chr7:104710916..104715928,6	K562	blood:

No data

Variant related genes	Relation type
KMT2E	TF binding region
ENSG00000239569	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000005483	chromatin interactions

Extended variants
information (count: 539 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:539 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552192570	chr7:104699683-104699684	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs28430714	chr7:104699897-104699898	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs199696420	chr7:104699903-104699904	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs528142850	chr7:104699911-104699912	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs562445449	chr7:104699917-104699918	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs547992215	chr7:104699979-104699980	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs566976322	chr7:104700025-104700026	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs567882577	chr7:104700036-104700037	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs75349403	chr7:104700046-104700047	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs180739729	chr7:104700160-104700161	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs186045547	chr7:104700168-104700169	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs60808750	chr7:104700183-104700184	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs539439555	chr7:104700189-104700190	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs553376125	chr7:104700198-104700199	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs149131866	chr7:104700221-104700222	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs11981399	chr7:104700223-104700224	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs116854893	chr7:104700237-104700238	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs575878427	chr7:104700289-104700290	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs190853365	chr7:104700307-104700308	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs7785197	chr7:104700321-104700322	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs557186885	chr7:104700344-104700345	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs564762525	chr7:104700345-104700346	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs578229916	chr7:104700396-104700397	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs540573606	chr7:104700421-104700422	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs111564725	chr7:104700428-104700429	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs112755822	chr7:104700431-104700432	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs67291226	chr7:104700446-104700447	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs13239176	chr7:104700466-104700467	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs13238981	chr7:104700470-104700471	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs527446778	chr7:104700481-104700482	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs559262257	chr7:104700493-104700494	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs568966904	chr7:104700504-104700505	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs528092915	chr7:104700531-104700532	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs548240845	chr7:104700568-104700569	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs369758790	chr7:104700593-104700594	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs561476163	chr7:104700600-104700601	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs536404537	chr7:104700612-104700613	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs59494471	chr7:104700634-104700635	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs181955251	chr7:104700673-104700674	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs555946927	chr7:104700684-104700685	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs139009194	chr7:104700687-104700688	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs539670698	chr7:104700746-104700747	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs186065606	chr7:104700759-104700760	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs6952534	chr7:104700760-104700761	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs535503761	chr7:104700772-104700773	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs555875491	chr7:104700779-104700780	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs368989131	chr7:104700830-104700831	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs114718463	chr7:104700832-104700833	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs373141082	chr7:104700896-104700897	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs538438609	chr7:104700917-104700918	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
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
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
Breast cancer	21858162	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16573809	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:620 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104658600-104703800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:104677800-104758200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:104678000-104812200	Strong transcription	Dnd41	blood
4	chr7:104680600-104727000	Strong transcription	Fetal Thymus	thymus
5	chr7:104681200-104758400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr7:104681200-104760400	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr7:104681400-104727000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr7:104682800-104700800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr7:104685400-104708000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr7:104685600-104703800	Weak transcription	Fetal Brain Male	brain
11	chr7:104685600-104704400	Weak transcription	Aorta	Aorta
12	chr7:104685600-104708200	Weak transcription	Esophagus	oesophagus
13	chr7:104685600-104709000	Weak transcription	Lung	lung
14	chr7:104685600-104720400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr7:104685600-104759000	Strong transcription	Primary B cells from peripheral blood	blood
16	chr7:104687600-104700400	Weak transcription	NHEK	skin
17	chr7:104687800-104721200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr7:104688000-104703600	Weak transcription	A549	lung
19	chr7:104688200-104707600	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr7:104688800-104701200	Weak transcription	Ovary	ovary
21	chr7:104688800-104701200	Weak transcription	Rectal Smooth Muscle	rectum
22	chr7:104688800-104707400	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr7:104689400-104708200	Weak transcription	NHLF	lung
24	chr7:104689600-104700600	Weak transcription	HMEC	breast
25	chr7:104689600-104705200	Weak transcription	Brain Germinal Matrix	brain
26	chr7:104689800-104700800	Weak transcription	Primary hematopoietic stem cells	blood
27	chr7:104689800-104701200	Weak transcription	HSMMtube	muscle
28	chr7:104689800-104703600	Weak transcription	Colonic Mucosa	Colon
29	chr7:104689800-104708200	Weak transcription	Pancreas	Pancrea
30	chr7:104690000-104703800	Weak transcription	Duodenum Mucosa	Duodenum
31	chr7:104691000-104703600	Weak transcription	Hela-S3	cervix
32	chr7:104691400-104703800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr7:104691400-104703800	Weak transcription	Fetal Muscle Leg	muscle
34	chr7:104692200-104703800	Weak transcription	Stomach Smooth Muscle	stomach
35	chr7:104692600-104700000	Genic enhancers	Primary T helper cells PMA-I stimulated	--
36	chr7:104692800-104702400	Weak transcription	NH-A	brain
37	chr7:104692800-104703800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr7:104694000-104699800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr7:104694000-104700000	Genic enhancers	Primary T helper cells fromperipheralblood	blood
40	chr7:104694000-104711200	Strong transcription	Primary B cells from cord blood	blood
41	chr7:104694400-104708200	Weak transcription	Gastric	stomach
42	chr7:104694600-104702400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr7:104694600-104703600	Weak transcription	Psoas Muscle	Psoas
44	chr7:104694600-104704400	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr7:104694600-104704400	Weak transcription	Small Intestine	intestine
46	chr7:104694600-104708200	Weak transcription	Right Atrium	heart
47	chr7:104694600-104708200	Weak transcription	Spleen	Spleen
48	chr7:104694800-104700600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr7:104695200-104708800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr7:104695400-104699800	Enhancers	Brain Angular Gyrus	brain

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