| Tag | Content |
|---|
EnhancerAtlas ID | HS145-25052 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr8:38785960-38787110 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr8:38786795-38786813 | CCTTCCTTCCCCCTTTCT | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr8:38785985-38786000 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
| SE_03039 | chr8:38786099-38787139 | Bladder | | SE_10916 | chr8:38778152-38824593 | CD20 | | SE_26945 | chr8:38786000-38787720 | Esophagus | | SE_35181 | chr8:38785179-38787166 | HeLa | | SE_40765 | chr8:38785036-38787708 | Left_Ventricle | | SE_42292 | chr8:38785116-38787438 | Lung | | SE_48823 | chr8:38786098-38787274 | Right_Atrium | | SE_49720 | chr8:38786169-38786994 | Right_Ventricle | | SE_50238 | chr8:38785987-38787300 | Sigmoid_Colon | | SE_52798 | chr8:38785973-38787569 | Small_Intestine | | SE_53542 | chr8:38786263-38787065 | Spleen |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I038923 | chr8 | 38781014 | 38787655 |
|
Enhancer Sequence | TTCACCATGT TGGCCAGGTT GGTCTTGAAC TCCTGACCTC AAGTGATCCA CCCGCCTTGG 60
CCTCCCAAAG TGTTGAGATT ACAGGCATGA ATCACCGCGC CCGGCCCGAC CTGGTCTTTA 120
AGTCTCTGTC ACCAGAGTTG GAAGACGGAA ATAAAGGGAA TGGGGGTGTG GCTGAGAGAC 180
TTAACACACA ATGAAACTTA TCCTGTCTAA AGCTGATACT GGTGTCTGTC AACAAGAAAT 240
CGACATCCAA GTAATAGAAT AAAAACATTA AGCCCACGCA GCAGAGGATG ATATAGAATC 300
GACTTCTCCT GAAGGGAAAG ATTAAATACA CACTTTGAAC TGGAGAATGG GGAGAGTAGC 360
TATCAGCGTG TCGTGTGTCC CCGCGTTAGC ATCAGCAAGT GGACCTACAG GGCAGAGGGG 420
AGGAGAGGTG TTTGGCCCTA GAGCAGCAGG TAGAGCCACG GCCCAGGTCA CCTGGTGCCT 480
GGGATTCGCT TGGCTCCCCT GCTTTGGTTG CTCATGTCAG GGTGAGGGCT TTGGAATGTG 540
GGGCAGCGGC AGCTATGCTC CTCCTTCCCA GTCCTGTCAC ACCGTTCTCC TACATTCAAA 600
TGTCTACTCT GAGCTATACC CCCTCTGCAG GCACATTCTT TTCTGTGAGT CTACATGGCC 660
GTGGCTTTTG GTGGCTGAGC TATGGTTTTA GCTCACAGAC AGCAATGTCA GCTCATGCCC 720
TAGCTCTGGG ATTACCAGGG GCGTCCCCTC CCTCCGTCTC CTGCTAGCTG CTTTTTACTG 780
TCTGCTGGAC ACCCCAGGGG CCTGTAAGAG AAGGTCAGAT GGCACCAGCA TCTCTCCTTC 840
CTTCCCCCTT TCTGCTCTGA ATCTCTGGTC TATTGGAGTT TGGCACCCAA GAGCCAGTTG 900
GACAAGTTCC TGCCCTGCCC AGCTTGGGCA ATGACACTGG GCCTCTTTTG GTGTAACCCT 960
GCTGGTCCTG CTTTTGTATT TACCTTTCAT TGATAATCAG CTCTTAGATA ATGTCTCATG 1020
GGAGATGGCA GGGCCTAAAG GAAAGTGCAT GGGATTTGGG AATCAGGAAG GGTTGGGCTT 1080
GAATACTGGC TCCGCTGCTT GCTGCCTGTG TGACCCTGGG CAGGTTCCTT CACCTGCCCC 1140
ATCCTTAGTT 1150
|
