| Tag | Content |
|---|
EnhancerAtlas ID | HS105-40522 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr19:45226940-45228410 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr19:45228160-45228171 | TTCTTATCTTC | + | 6.02 |
|
| | Number of super-enhancer constituents: 16 | ID | Coordinate | Tissue/cell |
| SE_09606 | chr19:45225026-45227473 | CD14 | | SE_23197 | chr19:45226609-45227960 | Colon_Crypt_1 | | SE_23197 | chr19:45227985-45229989 | Colon_Crypt_1 | | SE_23877 | chr19:45226698-45227829 | Colon_Crypt_2 | | SE_23877 | chr19:45228030-45229465 | Colon_Crypt_2 | | SE_26699 | chr19:45226534-45229277 | Esophagus | | SE_31568 | chr19:45227174-45229356 | Gastric | | SE_34750 | chr19:45226424-45229782 | HeLa | | SE_47531 | chr19:45227242-45227666 | Pancreas | | SE_47531 | chr19:45228001-45229336 | Pancreas | | SE_53360 | chr19:45226521-45227795 | Spleen | | SE_53360 | chr19:45227895-45229537 | Spleen | | SE_56197 | chr19:45227061-45227913 | u87 | | SE_56197 | chr19:45227922-45228447 | u87 | | SE_62704 | chr19:45221152-45271677 | Tonsil | | SE_65330 | chr19:45226619-45230111 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I044721 | chr19 | 45225041 | 45229949 |
|
Enhancer Sequence | AACAGCCTGT GCGAAGGCCT GAAGGTAAGT TTTGCATATG ACACCTTTGA GAAACTACTT 60
ATTGTTCAAC TGAAGCATAG GGTTGTTCAG AAGAAGCCAG CCTTGTGGCC GGGTGTGGAC 120
TTCCTCCCAG GGCACCAGGG AGCCACTGCA GAGTTGTGAG CAAGGGACAG ACAGAGGTAG 180
GCTTGTACTT CCAAGAGACT CCCCCAGCTG CCACATGCAG GGTGAATGGA ATGATGCACA 240
GAATCCAGTT TCAGGGGTAG TTTGGTACTT GGACCCAGGT CCCAGGGAGA GAGTCCAAGG 300
AGCCCTTCTC TGGTCTTCCA AGGAGCTGCT CTCCCCAAGC TCCGGATGGA AGGCGTGCCC 360
ATGGCAACCG CTAGGTGGTG CCCGTACACC ACCAGCCAGG TCTTTTTTTG CCAAAAGTAG 420
ATCAGGCCCA GAGCTGGGCA GAACTGCCCC TGGGTCAGGA GAGCAAATCG TCTCTGTCTT 480
TTGGTCCTGG CTCCCTGGCC AGGCATCCTG GGGCCATTTG ACTCCCAGGC TCAGGAAGGA 540
GCTGGCTGAG CTGCAGTGAG TATGTTCTTC GTCTCTTTCC TCACCTTGGA ATCTCAGACG 600
GGAGCACCCT GGCTCCCACT TCAGACAGGA AGATTCTTAC CTCCCTCATC AGACTAGCAG 660
GCTCTTTGTC TCCCCACCAG TTTGAGGGGC TCCCCATTTC TATCATTCAT TTGGAAGCTC 720
ATCAGCTCTC CCAGAAGGCA TGGGAGCCCT TCAACACCCC CATCAGACTA GGACTACCCA 780
TCTCCCCCAT CAAATTAGAA CTGCATTGTC TCACACATCA AAGTATCACT CCTGGCCAGG 840
TGCAGTGGCT CCCGCCTGTA ATCCAAGCAC TTTGGGAGGC CGAGGCAGGA GGATCACCTG 900
AGGTCAGAAA TTCAAGACAA ACCTGGCCAA CACGGTGAAA CCCGGTCTCT ACTAAAAATA 960
ACAAATTAGC CAGGCGTGGT GGTGTGCGTC TGTAATCCCA GCTACTCAGG AGGCTGAGGC 1020
AGGAGAATCG CTTGAACCCA GGAGGCACAG GTTGCAGTGA GCCAAGATCA CACCACTGCA 1080
CTCCAGCCTG GGCGACAGAG CGAGACTCTG ACTCACAAAA ATAAATACAT TGTCTTACAC 1140
ATCAGAATGT TGCTCCTTAC CTCCCCTGGC AGACTGGAAA TATAGACTGG ACACTCGTTC 1200
TTGCTGCACA GGACTGGAGC TTCTTATCTT CTTCATTGGA TTTGGACAGT CCTGTCTCCC 1260
TCATGGGATT TGGTGAGAGC TCCTTAGTTT CCTTATTTTT CCCACTGTGT TGGGCCACCT 1320
TGTCCCCACC ATCAGATTGG GGAACACCTT GTCTCCCAGT CAGACCAGAG GGGCGGACTC 1380
CTCTGCCCTT GCAAAGGTTC CTAGGTCCTT CTTACATCCA TAGGAGGAAC CATGCCTATT 1440
TTACCAAGAG GGAAACTGAG GCACAGAGAA 1470
|
