Tag | Content |
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EnhancerAtlas ID | HS158-55818 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr8:101475260-101476570 |
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 | AGACAGAACT GATTCTAGCT CAGCCCACAG GAAGGGTAGC CTTGCTCTCA GAAACCAAAT 60 CTCTGGCAAG GCTGCCTTTA GGGTCAGATT CAGTGACATT GGACTCCATG CTGGGGCAGA 120 CCCAATCGGT GTGCCTAGGC CAAGATTCAG CAGGCCACAG ATGCCTGGGG AATGAGCTTG 180 ACCTCCTGGA GTCACTCCTT AAGAGAAGCA CCCAGCCTAT ATCCCTGGGT TGTCCCACTT 240 CCAACACAGC CCATATAATG CTGAAATTCA TATGCCATTT ACTAACCTGT GCCAGATCAT 300 CATATCACCC TCCCCTCTTT CTCTCAAGTG TGGTAGAAAT GGCTAGTTGA CCCCTGAAAA 360 GTCATGATCT CCTTGACTCC TTGATCTGTA TAGTATGAAC TTGCTGTTGA GAAGCAGGTG 420 ACTAACCAGG GACTCCATTT CCCAGCCTCT CAACCCACCC CATGTCCTTC ACTCTGGCCA 480 GTGAAATAAG AGCCTGAGAG ATGTGTCACT TTCTGGCTGA GGTGGTTAAG TATCCAGTGT 540 GGCTTTCCTC ACTCTCTTCC CCAGCTTGTA TCACTAAAGG ACAGAGGCCT GGATCCCTGA 600 GTAGCTGGGT GGAGGAAGAG CCCAGGACTG CTGCCTGACC AGGAATGTCT GATTAGAGTT 660 TGTGTGAGCC CGAAATACAC TTTTGTGTTC AGCTGTTAAT ACTGTGGGTT TTTCATTGCA 720 GCGGTTCGCT GTGTTGACTA AGATAATGCC CATGCAGCAT TTCCTAAGCA GCGCATCCTG 780 TGATAGTGGG ATTTTCCCCT GCTCCTATCT TTCTTTGTGC AGAGAACACC AGTGCTGCCC 840 ACGTGCCCTG TGGTCTTGTT TGAGTCTCTG TATACCTCTC TCTCCACCCT CCCGAATGGA 900 ACCTCGCTTT GTGAGGAGGC AGTAGAGCAT GGGCAGAAGT TACAAGCGTA GTTTCTGATC 960 AGATTGCTTA GGTTCAAATC CTGACCCCAC CACTTACAAA CATGTGAGGC CTTGAGCAAA 1020 TGGCTTAACT TCTCTGAGCT TTAAATTCTC TCTCTAACAG AGGGAGAGTA CCTTGCAGAG 1080 TTGTCATGCT GAATAAACAG AACAGTGTAA AGTACCTGGC ACATAATCAA CATAGTAAAT 1140 ATTAGTATTG TTAGATGGCT GTTACCTACT GAGCCAGCTT CAGCATAATA GATATGCAGA 1200 TTGACTGCAA CCAATCAGCA TCATTGCCAC TCTTCTTTCT CCTCCTTTCT TCTATTCATG 1260 TCAGTAATTC CCACCAGTAA TGCACAACAG TTTTCTTTCA TGGGTACTGG 1310
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