Tag | Content |
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EnhancerAtlas ID | HS108-39669 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr8:101475340-101476590 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYC | MA0147.3 | chr8:101476096-101476108 | GCCCACGTGCCC | + | 6.44 | ZNF263 | MA0528.1 | chr8:101476487-101476508 | CACTCTTCTTTCTCCTCCTTT | - | 6.01 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_18537 | chr8:101474767-101476978 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19357 | chr8:101474800-101476994 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_22743 | chr8:101474949-101476249 | CD8_primiary | SE_27991 | chr8:101475318-101476841 | Fetal_Intestine | SE_28830 | chr8:101475112-101476756 | Fetal_Intestine_Large | SE_32305 | chr8:101475087-101476367 | Gastric | SE_32533 | chr8:101474347-101477244 | GM12878 | SE_34085 | chr8:101475071-101477112 | HCC1954 | SE_47999 | chr8:101475715-101476254 | Pancreas | SE_62291 | chr8:101421434-101542088 | Tonsil | SE_65844 | chr8:101476363-101477325 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I100462 | chr8 | 101475138 | 101477142 |
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Enhancer Sequence | GGGTCAGATT CAGTGACATT GGACTCCATG CTGGGGCAGA CCCAATCGGT GTGCCTAGGC 60 CAAGATTCAG CAGGCCACAG ATGCCTGGGG AATGAGCTTG ACCTCCTGGA GTCACTCCTT 120 AAGAGAAGCA CCCAGCCTAT ATCCCTGGGT TGTCCCACTT CCAACACAGC CCATATAATG 180 CTGAAATTCA TATGCCATTT ACTAACCTGT GCCAGATCAT CATATCACCC TCCCCTCTTT 240 CTCTCAAGTG TGGTAGAAAT GGCTAGTTGA CCCCTGAAAA GTCATGATCT CCTTGACTCC 300 TTGATCTGTA TAGTATGAAC TTGCTGTTGA GAAGCAGGTG ACTAACCAGG GACTCCATTT 360 CCCAGCCTCT CAACCCACCC CATGTCCTTC ACTCTGGCCA GTGAAATAAG AGCCTGAGAG 420 ATGTGTCACT TTCTGGCTGA GGTGGTTAAG TATCCAGTGT GGCTTTCCTC ACTCTCTTCC 480 CCAGCTTGTA TCACTAAAGG ACAGAGGCCT GGATCCCTGA GTAGCTGGGT GGAGGAAGAG 540 CCCAGGACTG CTGCCTGACC AGGAATGTCT GATTAGAGTT TGTGTGAGCC CGAAATACAC 600 TTTTGTGTTC AGCTGTTAAT ACTGTGGGTT TTTCATTGCA GCGGTTCGCT GTGTTGACTA 660 AGATAATGCC CATGCAGCAT TTCCTAAGCA GCGCATCCTG TGATAGTGGG ATTTTCCCCT 720 GCTCCTATCT TTCTTTGTGC AGAGAACACC AGTGCTGCCC ACGTGCCCTG TGGTCTTGTT 780 TGAGTCTCTG TATACCTCTC TCTCCACCCT CCCGAATGGA ACCTCGCTTT GTGAGGAGGC 840 AGTAGAGCAT GGGCAGAAGT TACAAGCGTA GTTTCTGATC AGATTGCTTA GGTTCAAATC 900 CTGACCCCAC CACTTACAAA CATGTGAGGC CTTGAGCAAA TGGCTTAACT TCTCTGAGCT 960 TTAAATTCTC TCTCTAACAG AGGGAGAGTA CCTTGCAGAG TTGTCATGCT GAATAAACAG 1020 AACAGTGTAA AGTACCTGGC ACATAATCAA CATAGTAAAT ATTAGTATTG TTAGATGGCT 1080 GTTACCTACT GAGCCAGCTT CAGCATAATA GATATGCAGA TTGACTGCAA CCAATCAGCA 1140 TCATTGCCAC TCTTCTTTCT CCTCCTTTCT TCTATTCATG TCAGTAATTC CCACCAGTAA 1200 TGCACAACAG TTTTCTTTCA TGGGTACTGG TGTTTCTTCT AGCTCTGTAC 1250
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