| Tag | Content |
|---|
EnhancerAtlas ID | HS108-16900 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:40593340-40594580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata4 | MA0482.1 | chr17:40594301-40594312 | TCTTATCTCTT | + | 6.02 | | MEF2A | MA0052.3 | chr17:40594172-40594184 | GCTATTTTTAGT | - | 6.18 | | MEF2B | MA0660.1 | chr17:40594172-40594184 | GCTATTTTTAGT | - | 6.62 | | MEF2C | MA0497.1 | chr17:40594171-40594186 | AGCTATTTTTAGTAG | - | 6.15 | | Nr2f6(var.2) | MA0728.1 | chr17:40594220-40594235 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_29743 | chr17:40593015-40594194 | Fetal_Muscle | | SE_53648 | chr17:40593725-40594956 | Spleen |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr17 | 40593688 | 40594014 | | chr17 | 40594296 | 40594487 | | chr17 | 40593785 | 40594533 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I042441 | chr17 | 40593308 | 40594550 |
|
Enhancer Sequence | TATACATTTG TAGAGATAGA GCTAGAGGTT TGGCCTCTGT GTGTTGAAGG CTTAGAAGCA 60
ATAACACAAT GTAACAATGA GCAGGCTTGG TACCAAGATC TTGGTTTCTA AATATTATTC 120
CTCACAACAA AGAAACAGCT TCTTAGAGAA ATGGATGACT TCAGGGCTGG AACAAGGAAA 180
GTATAAGCTA AGCTTAAAAT ATCCTATTGT GATAGAAATT AAGGAAGTCC CCTGCCACCC 240
CCAACACCCC AGCAAAATGA TGGGAATATG TCAAAAAACA CAGGAGGAAG TTCCAATTAT 300
GGCTGAGTAA TTCCCATCAC ACCAAGTCTT CTGTAAATAA GAATGATATA CTCAGAGCAA 360
AATATTAAAG AACAAACAAA AACTACCTGA AGGCATTAGC AAACAACAGG AGGAATATAC 420
TGCACAGAGG TGGATACCTG GAAGAGAAGA GGACTGAATG GGTTTCCTGT GTTTTTACAG 480
CTTTTAGTCT AAGGGAAGTC CAAAGTCTGC AAAGTGAGTG GTTAAAACAA AGCTGGGGGT 540
AGTGGTGTGC GCCTGTAGTC TCACCTACTC AGAAGGCTGA CGTGTGAGGA AACCGTGAGC 600
ACAGGAGTTC AAGGCTGTAG AGCACTAAGA TTGTGCCTGT GAATACCCAC TGTATTCCAA 660
CCTAGGCAAC ACAGTAAGAC CTCATCTCTT TTTTTTTTTT TTTTTTTTGA GACAGAGTTT 720
CACTCTGTTG CTCAGGCTGG AGTACAGTGG CGTGATCTCA GCTCACAGCA ACCTCTGCCT 780
TCCGGGTTCA AGTGATTCTC CTGCCTCGGT CTCTTGAGTA GCTGGGACTA CAGCTATTTT 840
TAGTAGAGAC AGGGTTTCAC CATGTTGCCC GGGCTGGTCT TGAACTCCTG ACCTCAGGTG 900
ATCAGCCCAT TTCAGCCTTC CAAAGTGCTG GGATTACAGG CATGAACCAC TGTGCTCGAG 960
ATCTTATCTC TTAAAACGAC GACAACAACA ACAAAAACAA AACAACAAAA ACCCAAACCC 1020
TGCAGTCTTA CTAGCTTGAA TTGTTCAGGG CAACCCCAGC AGGTGGAAAT AATGGGAGGA 1080
AATCCTATCA AAATAAGAGC CACAGAGAGG GAGGCTCAAA TTCTGTGCAT AAACTATAGT 1140
CCCAGCTACT CGGGAGTCCC AGTACCTGTA GTCCCAGCTA CTTGGGAGGT TGAGGTGGGA 1200
GGCTCGCTTA AGCCCAGAAA GTCAAGGCTG TAGTGAGCTG 1240
|
