| Tag | Content |
|---|
EnhancerAtlas ID | HS108-08628 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr11:117777000-117778500 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EGR1 | MA0162.3 | chr11:117778070-117778084 | GCTGCGTGGGCGTG | - | 6.15 | | EGR2 | MA0472.2 | chr11:117778072-117778083 | TGCGTGGGCGT | - | 6.62 | | EGR3 | MA0732.1 | chr11:117778070-117778085 | GCTGCGTGGGCGTGG | - | 6.32 | | SP8 | MA0747.1 | chr11:117778022-117778034 | GGTGGGCGTGTC | - | 6.02 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_25531 | chr11:117777916-117780553 | DND41 | | SE_53890 | chr11:117777987-117778840 | Spleen | | SE_59013 | chr11:117768550-117824927 | Ly3 | | SE_61192 | chr11:117757750-117831515 | HBL1 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I117906 | chr11 | 117777561 | 117781639 |
|
Enhancer Sequence | CACAGACCAC AGAATTCCTG CTAACTTGAT CCCACATTCA GAAATATTAT ATTTAGAAGT 60
CACTGTTATA TATCACTTCA TAAGCTCTGA GGACTGGTGT CCCTAGGGGG ACCAGGGCAT 120
TGACCAACAC ATCTGAGTTT GCAGGAGGAA AATATTAGTT AATAGAATGT TTGCAGTATT 180
CTCAACCCTT TGTTATATTC ACTGCAGTAT TCTGCACCTA AGATAATGCC TGTCACATAT 240
TAAGTGCTCA ATAAATGTTT AAAAAGATAG AGACAAGGCA GGAAGCGTAG ATGGGAAGGA 300
TGATTTTAAA TTCTTCTCCC ATAAATTGGA ATTAGGCTTT AAACATTGGT GTCTACCTCA 360
CTTTTGTCTG CTAGAGAGTA AACAAAAAAT AGATGAAGGA ATAGCATGCA TTATTAACAA 420
AAATGCAGCA TAGGATTTTT TTTCTATGCC CCTTTTTGAG ATGTAAAGTT TTAAAAACAT 480
GTAACACTGT TACATGATCC ATCGTTAGAT ATTTCACTGT TTTTTATGGG GGAATTAAAT 540
TTACCAGTGA ACTTTCACAA GCAAAAGTAC TGTGACTTCT AGTGCTCCAC CTGCCAAATG 600
AGTTTAAGAA AATCAGTCCT GATTTCTAAA CCAAAAATCA GGGCACATGT TCTGGCCACA 660
GGACTACATA CATCTGAGCT GTGATTCTCA GACTAAGGGT CTGCTTCCTG CCCAAAAGCC 720
TATTGGAGCC TGGAGGGAGA CTATTACGTT TGAAAAGCAT ACGCAATGTG AGAATAGCTT 780
TCATTCGCTT TTAGAAATTA TTTAGTTTTG GAATTCCAAA TAATATTAAG GGGTGGAGGG 840
TGGGTGGGAG GTAAGATTTG GATGTTTAGC CAAATACAGC CTGGGTTTGA CAAGGTGAGA 900
AGGCCTGCTC TGGTCCTGCA GTCTGTGCCC TTCTTGTGTG CTGAGCGGCA GGGCAGGAGG 960
TAGCGGGCAT CCCTCACCTC AGCCCTGGAC TCCACAGACA AGGATGGAGT TTCAGAAAGG 1020
CTGGTGGGCG TGTCGTGTCG TGTCGGGGCG TGGCTACGAG TGGGTGTGAC GCTGCGTGGG 1080
CGTGGTTCTG GGCTAGCGCT GCCCAACCGA GCTCTACCCA GGGATCCTCC TCCTCACCCC 1140
ACTCTGATGA TCTAACTGCT CTGACTCATG ATAGACACCG CCTCCATAAT TAATGTGCGA 1200
GGAAACACCA GCTCACAGGC TCAGAGCACG AGAATGGCTG GACTAACCAG AGAGTCCTCC 1260
GAGGCTTCCA GAAATCCCGG TACTCCTCCT CCCTCTCCCA CCTTTACAGA TGCTTATGCC 1320
AGAGGGCTCT GGCTCCATTC TTCAGGGTCC TCCCTGAGCC CCCATTACCT GTCTTCTCCA 1380
ATCTTTTCGG GACCCACCTT GGCTATCCTT CCTCTGCTGA GCTTCCCCTA GCCTGCCAGG 1440
ATGATTAGTT GCTCCCGCCT ATGCCACCAT AGCTCCCTGC TCCCCGAAAA CATCGTATAA 1500
|
