| Tag | Content |
|---|
EnhancerAtlas ID | HS108-04079 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:211821560-211822710 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr1:211822406-211822421 | AATTAATAATTAATC | + | 6.08 | | JUN(var.2) | MA0489.1 | chr1:211821818-211821832 | AAGAAATGACTCAT | + | 7.82 | | NKX2-5 | MA0063.2 | chr1:211822174-211822184 | ACCACTTGAG | + | 6.02 | | Sox6 | MA0515.1 | chr1:211821580-211821590 | AAAACAATGG | - | 6.02 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_28267 | chr1:211819385-211824621 | Fetal_Intestine | | SE_29189 | chr1:211819363-211824564 | Fetal_Intestine_Large | | SE_34866 | chr1:211820487-211823612 | HeLa | | SE_54270 | chr1:211820880-211822806 | Spleen |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I211646 | chr1 | 211819618 | 211824332 |
|
Enhancer Sequence | TAAATTAATA TTCCTGTGTT AAAACAATGG CCCAGACAGG GATTCCTCCA GGTGGGAGGT 60
GCCCAGGGAT GGGGTCACGT TCAGAGGACA GAAGTCCTTG TGTCTGTGTG ACTTTGGATG 120
GGTCACTTCC CTCTCTGAAT CGTTATTTTC TCCATGAGAA CAATATCTAC CCAGTCTAGT 180
TATGGTGTTG TTTGGGAATC GTCTGGTATC CTGTCTTGTG ACAGTGCTTT GAAAACTGCA 240
GTTAAGTAAC ACAAAGGTAA GAAATGACTC ATGCCAGGAA AGGGAATAGC ATGAGGCCCA 300
GCTCTGATAT GCAAAGGCCT CTCAGATTCT TAGAGAATAT TATTGGCTCT CACACCACCA 360
GCTGCTCCCA GTGAACTTGG CCTTCGCCCC CAGGAATGGC TGATAAAGGC CTTCACTGCT 420
TTCCACTTCT GAGCTGATGG GACTGTTTTA GCTGACCCAG CTAAAACCAT GATTAAGTGG 480
CTGGATTTGG AAAAGAAGTG TTGGGGCTCA TGGTTCACAG ATACGTTTCT GGGTTGTTAT 540
AAAAATTAAT AATTAGGCTG GGTGCGGTGG CTCACTCCTG TAATCCCAGC ACTTTGGGAG 600
GCCGAAGCAG GAGGACCACT TGAGGTCAGG AGCTCAAGAC TAGCCTGGCC AACATGGCGA 660
AACCCTGCCT CTACTAATAA TACAAAAATT AGCCGGATGT GGTGGCTCAT GCCTGTAATC 720
TCAGCTACTC AGGAGGCTGA GACAGGAGAA TCGCTTGAAC CTGGGAGGTG GAGGTTGCAG 780
TGAGCTGAGA TTGTGCCACT GCACTCCAGT CTGGGTGACA GAGTGAAAAT ATGTCTCAAA 840
AAACAAAATT AATAATTAAT CCTCTCCTGC ATGCTGGAGG GGAACTGCCA GCAGCCTCCG 900
AGTTATGGAG AGCACTCCTG GCCACCAGGC TCCCCGTGAG TCCTGGCTCC GTGTGAGCCC 960
AGGCCAGCCC TCCTCTCTAC TGCCCTCCAC TGGGTCCCCA TGGTAAAATA AGGGGCTGCA 1020
CTTGATGAAA GTGAATTTGC AACTGAAAAA ATATGTAATA ATAAAGCCAG ATCCCTTCTA 1080
AGAGACTTTA AAGGTCTTCC AACTTGTCTT CTTCCTGCTC CCAGTAGATT ATGTCCCCTG 1140
TCCTCATGCC 1150
|
