| Tag | Content |
|---|
EnhancerAtlas ID | HS113-38096 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr9:100904070-100906020 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr9:100905624-100905637 | AGCAGCTGTTCCT | + | 7.22 | | TFAP2C | MA0524.2 | chr9:100905474-100905486 | TGCCCTGGGGCA | + | 6.44 | | TFAP2C | MA0524.2 | chr9:100905474-100905486 | TGCCCTGGGGCA | - | 7.22 | | ZNF263 | MA0528.1 | chr9:100905096-100905117 | CCTCCCCTCCGCCCCACCTCC | - | 6.07 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_09950 | chr9:100904103-100905141 | CD14 | | SE_24386 | chr9:100904263-100906392 | Colon_Crypt_2 | | SE_26852 | chr9:100904207-100909935 | Esophagus | | SE_27659 | chr9:100903802-100910551 | Fetal_Intestine | | SE_28584 | chr9:100903818-100910565 | Fetal_Intestine_Large | | SE_42027 | chr9:100904412-100905212 | LNCaP | | SE_53152 | chr9:100904184-100910435 | Small_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I098141 | chr9 | 100904020 | 100910418 |
|
Enhancer Sequence | AATGAATAAT CATTTCTTCC TTGCAGGATT GTTGAGAGTT AAATGAGATA CTATGCATGA 60
AGAGCCCAAC AGTCAGGTGT TACTGTAAGT GCTCAGTAAC AGAAGCTACT ATTATATGTA 120
TATGTATGTA TATTTGTATG TCAAAACTGA GAAAAAAAAA CTAAAAGGAA TGAGCCAAAA 180
TGTTAATCAT GGTTATATCT AGATGGTGGA ATAAATGGCT GGCTTTAATA TCTTTGTCTT 240
ATTTTTAGCT ATGTAAGTTT TGCAATTAAA AAAGGTGTTT AAAAACAAAA ATACAGATTT 300
TCTGAAAAAA TGGGTCCATC CAGGATTAGC CAAAAACTTC TGTTATAAAA CTGTAGCTCT 360
TGAAGGGCTC TAGAGACCAG GAATGGAGCC CACAGCTGCA CTGTCTTATC CTGCACCTGT 420
GGCAGGCATT GCGAATGGAT CCCAGCACCC TCTCTCGGAC CTCAGACTTG GGGAAATCCA 480
GCATGGAGTA GGGACTTGCC CAGGGTCACT GCAAAGGTGA GGGGCAGAGC TGGGCTTGAG 540
CCCAGGCCTC TGGTTCCCCA AGTGTGAGCC TGGTGCTGTA CTTCCTGTGC TCTGAGGGAG 600
CACCAGTGAG TGCTCTGTGA GTCCCTGCCC TGGCCTCCTT CCTGCACACA GCCTTTCCTT 660
TCTCTGGGAT CATTTCCTGG GTCAAAGGCC ATGAGCAGTA CTGTGTCTTT GGCTGTGGGG 720
CACTGATTGC TCTCCGGGCC TTTAGACTCT GGCCCAGGGC CATGCCCCAA TTTCCGCAGT 780
GCGGTTTCCC AAGAAAAGCC AGATGAGCCA ATAGTCAGGC TGCCCTCGGG CTGACGGGAG 840
GCAAAGTGCC CAGGAGCCCC ATTCAGACAC ACACCTCCCA CCTCCCACAG ACTCAGGGAA 900
GGCGCCTTAG GGTTGGGCGT GGCTCAGAAG GGCCTAGCCC TAGACAGCTT CTCTTCCTTC 960
TCAGCCTTCT CTTCCTTCTC AGCTGATGAG GGAAGGCTGC CCACTCACAC CCCAGCCCAC 1020
CCCAGCCCTC CCCTCCGCCC CACCTCCCCT GCCCTGCCCT GCCCTGCGCT GCCCTGCGCT 1080
GCCCTGCGCT GCCCTGCCCT GGGCTGGCAG ATTGCTCTGC TTCTAAAAGG TTTTACGCTG 1140
AGGACCACAG GCAGGAGCGG ACATTAGCCA GCCTGGTGGG CTATTGACTG AGCTGCTAAA 1200
AGCCTGTCAG GGACATTTAT CATCAGGAGG CCATTTCCAC CTTCTGCCCA TTAGGCCAGC 1260
ACTCAGCCAG AAACAGGCTT CTGATGGATG TGGTGTACAA GCTCTAAATC AGGGGAGACA 1320
CGCCTGCTCC CCTCGCAGAC CCCACAGAAC CCTGGCTTGG GCCGCCCTGC CTGGAGAGGC 1380
ATCACCTCCA AGTCTCCAAG GGGCTGCCCT GGGGCAGAGG GGGAAGACAG GACAGAAGGA 1440
CCCAGGAGGA GTCAGGCGGG TGGGGGACCA GACTGGGGAC TCTCTACGGC TGACCTCCAT 1500
TGCCAGAAAG GGAGAGGTTG TGAGGCCACT GTCACGACCC TCAGCAGTCA AGGGAGCAGC 1560
TGTTCCTACA ACAGCATCAT AGTCATGGCC TCAAATGAGC ATCCCAACAG CTCAGGGTGG 1620
AGACTGGGAG GCAGGGGTGG CAGGACGGGC AGAGGGAGGA CACACAGTGT AGCAGAGGTG 1680
AAGTGGGCAG GCAGACTCTG GCTTCCAGGG GTGGAATCCC TGCCACATCC CTTACCATGG 1740
TGCAGCCTTG GGCAAGTGAC CTCAGTTCTC TATGCCTCAG TTTCCTTATC TACGAAATGA 1800
CAACAGTAGT AGCACCTCAT TCACAGTAAA GCACTGAAGA CGGTGCCCAG TACTTGCTAA 1860
GTACTCAGTA CATTAGCCAG GAGAAGCTCA TCACAGCTCA TTACCATTAC CCAGTTTTAT 1920
TGTTGCTCAG TATGTTTCAG GGGCCAGGGG 1950
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