| Tag | Content |
|---|
EnhancerAtlas ID | HS052-12145 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr14:100882800-100884360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr14:100882890-100882908 | CTTTCCTTCCTTCTTTTC | - | 7.57 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_23539 | chr14:100881896-100884362 | Colon_Crypt_1 | | SE_24202 | chr14:100882703-100883278 | Colon_Crypt_2 | | SE_24202 | chr14:100883297-100883955 | Colon_Crypt_2 | | SE_24202 | chr14:100883966-100884294 | Colon_Crypt_2 | | SE_33398 | chr14:100880989-100894517 | H2171 | | SE_34657 | chr14:100880856-100885474 | HeLa | | SE_50425 | chr14:100881913-100884404 | Sigmoid_Colon | | SE_65652 | chr14:100882531-100884455 | Pancreatic_islets | | SE_66879 | chr14:100880989-100894517 | H2171 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 100883887 | 100884104 | | chr14 | 100883227 | 100884269 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I100416 | chr14 | 100882682 | 100884847 |
|
Enhancer Sequence | ATTTCTGTTC CTATCACAAA CTGCCTGCTG TGTGCCTTGA ATTCTTTCCA GCTCTTTCCC 60
AAACATGACA CACCCTTTTA GGCCTTTTCC CTTTCCTTCC TTCTTTTCAG GCAAAGTCTT 120
CCTTATCCCC CTGGACTTGG CTCAAGGGTC CCCTTCTCTC TGTACCCATT CCTTGAGGTT 180
GCCTTTCTCC CTTGTCTCCA GACTGCATAA ATGGCAGTGT GGCCTGTGTT GCTGTAGCAC 240
CATGTGCACC TGGGCTGTGC CCCGGCAGTG TTCTGTCTTT GGGCTCACTG GGGAGGGAGC 300
ACTGGACCAT CGTCCCCAGA TGCCCAGGGA GAAGCTTGGT GCTCGTTACT GACTGTAGGG 360
TACTTTTCTG TAGCAGGCAC TTGGGGCTCA CTTATGGGAC CCAGTAACTT CACAGTCATG 420
AGGTACTTGA TTTGAACTGA GGAGAAAATG TGTCAATACC TTTCCCAGGG AGAGTCACCC 480
TCACAAACCT TGGTCTGGAA GGCCCATCTT AGCCCAGGGG TGAGATCTTG CGTGGATGAT 540
TCAGAAGTCA CAGTATTCCT GAAAACTAGT GACTCAACAG AATTATATGG CTTTGGGAGA 600
AAGAGTCCCT CCAGGGGCAA TCCAACTACC ACAGGCCAGG GGCCAAGCTT TGGTGAGCCG 660
AGCCTGGGCC CTGCCCCTCC CTTCTCTATG GGCCTAGGGT TGCTGTGCTG TGTGTGGCAT 720
GGCCAGAGTC CTCCGCTCAT CTCCTCACCA TCTGTTACTT GTGCGTGTCT CCTGTGCCAG 780
GCCTGGTGCT GACACTAGCT CAGGGAGAGA GGCAGCCGTA CCTGGAGGAG CTGCTTAGTA 840
GGACACTTGG CACATGCCAC ATGCTTTGCA GACTTCTCAG TCTCCCAGCC ACTCAGGGAT 900
TTGTGGGACT GAGTATCTCA GATCCAAGGT GGTCAGGCGA GGGTGCAGGG AGATGGAGCC 960
ATGTGTGGGG CCAGGCTCTT TCCCATGACC TAGGTGCCCC TTCCAACCCC CACCATCCTG 1020
TTAAGACCCT GAGCAGCCAG GCTGGTTGCT CCAGCCACTC TTCCCTGGTG GCTCCCCTTT 1080
CCAGTTCTGA GGCTACTGCG AGTCACCTTC CTCCTCCAGG GAGGGAGAGA GCTGCCTGAG 1140
CATTACCTCT GCTTGCGGAT GGGGGTGCTA GAGACCGAGC CTTTTCCTTG TTGTCTCTGC 1200
CAGTGAGGCT CTGGAGAGTG AGTCAGGAAT ACAGCTGCAC AAATCGCCCT TACTTTGATA 1260
CTGTGTGATT GGTCTGCAAG ACAGACACAG GGCTGACATC GCATTTTCTG CCTGACTTCT 1320
TCCTGGCTGC AGTGACCCTG AGCTGTTCCT AGCCTTCCAT CGTTTCTGTT GTGGACAGGC 1380
GTGTCATGCT GCCCCTGTTC CTCCTGCCCT GGCCTGGCTA CTTAGGCTCT TGTGCATGTG 1440
CTCATAGGTT CTCATGAAGG TTGTTCTTAG TTTGCTTATG TCTTTTTTTT TTTTTTGAGA 1500
CGGAGGCTCG CTCTGTCGCC CAGGCTGGAG TGCAGTGGCA CCATCTCAGC TCACTGTAAC 1560
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