| Tag | Content |
|---|
EnhancerAtlas ID | HS103-17276 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr4:10032950-10034070 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr4:10033477-10033491 | TGTCCCCTGGGAAT | - | 6.04 | | LHX2 | MA0700.1 | chr4:10033766-10033776 | ACTAATTAAC | + | 6.02 | | NFKB1 | MA0105.4 | chr4:10033219-10033232 | AGGGGATCCCCCA | + | 6.04 | | RARA(var.2) | MA0730.1 | chr4:10033504-10033521 | GGGTCACCAAGAGGTCA | + | 7.33 | | RREB1 | MA0073.1 | chr4:10033910-10033930 | GGGTTGTGGGTTGGGTGGGG | - | 6.23 | | RREB1 | MA0073.1 | chr4:10033906-10033926 | TGTGGGGTTGTGGGTTGGGT | - | 6.74 | | RREB1 | MA0073.1 | chr4:10033911-10033931 | GGTTGTGGGTTGGGTGGGGG | - | 7.49 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_10112 | chr4:10033319-10035658 | CD14 | | SE_36611 | chr4:10033654-10035411 | HMEC | | SE_53020 | chr4:10032399-10036919 | Small_Intestine |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH04I010030 | chr4 | 10032374 | 10033550 | | GH04I010032 | chr4 | 10033826 | 10035805 |
|
Enhancer Sequence | CAGGCTGGCC CATGACCTTT CATTCCCAGC AAAGCCTAAT TGCATGAAAG TGCCACACAG 60
TTTGAAAACA GGCTGCATTA TTTACGGATC CAATCGAATT AGCTTGCAAT TCCCAGACCA 120
GCTTTAGATC AATGAGATGC ATTGTGTGTT CTCCCACGTG GGTAAGGAGG CCTCTCTGCT 180
CCTGGGCAGC CCAAGACAGC TCTGTAGTCA GAAGATGAGT CTTTGACGGC TTCCAAAGCA 240
TCGTCTTAAT GGGCACAGTA GGATGCTAGA GGGGATCCCC CAAATCTATT TCATTTTTAA 300
ACAAAAAAGA GTGAATGTTT CTGCTTATGA AATTCTGGAA AGTTAGTCCT AGCCAGGAAG 360
GGGCCGGAGG ACTCCGTTGC AGAACTCCTG CCTTGTGGAA ATCAGGAAAC CGAGACTGAG 420
TGAAGCAGCC AGTTAGCGGA GCTGGAGAAG GATGTCCCAT GTCCTGAGAC TGACCCCATT 480
CTTGATCCCA AGCACTGTAA ATACTGTGCT GATTAAGATT TAGCCACTGT CCCCTGGGAA 540
TGCACTGGGA ATGAGGGTCA CCAAGAGGTC ACAGGCATAA AAAGAACCTT CCTGCATATT 600
GTTATCTGTG CTCTGACAGA GGCAAAACAG GGCGCTGGAA AGGAGGCAGC GTGTTTGTTT 660
TAGCTTCACT CATTCATGCG TTCACTTATT CATCCGATGG TGTATATTGA GCACCTACCT 720
TGTGTCAGGC CCACCCTATT CTAGGCATTA TGGACCCAGA GCCAACAAGG TGGGAAAAGT 780
CCCATCTCCA GCTCCTCACA CCAAGTGGGG CATCAGACTA ATTAACCAAC ACACTTAAAT 840
TGACGTTCAG GTACCATTAT AGCAAACTCT AGAAAGCAGT GTAAGGTGAT GAGAGAGGCA 900
ATATCAGGAA ATTCTGATGT GATGGGAGGA GTGGGAATTA ACTGAACATC TGTAGATGTG 960
GGGTTGTGGG TTGGGTGGGG GTCCAGGCAG AAGGAGCAGC AAGGGCCAGG GCTGGAAAGA 1020
GCTTGTGTGT GAGGGTTTCA GGGACTGGTG TGGTGGGGTT GTCAAGGCCT GTCTTGTGAC 1080
GTGGTTAGGG ATGTGGGACT GCAGCCTAAG AGCCATGGGA 1120
|
