| Tag | Content |
|---|
EnhancerAtlas ID | HS129-19364 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr2:37750860-37751780 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EN2 | MA0642.1 | chr2:37751062-37751072 | GCTAATTGGG | - | 6.02 | | MAX | MA0058.3 | chr2:37751423-37751433 | AGCACGTGGT | - | 6.02 | | Nkx2-5(var.2) | MA0503.1 | chr2:37751561-37751572 | AAGCACTCAAG | + | 6.02 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I037523 | chr2 | 37750153 | 37753678 |
|
Enhancer Sequence | CAAATCCTCA GTCCTCTCTG CAACTGGAGT TTTCTTTAAG ATTGTCAAAT AAATATGTTT 60
GGGGAAGATG GTAATTAAGT GTGAACAGAT GGTTGTTTTT AGCTGAGATA TTAAGTCTCA 120
GTGTTTAATA GAATGATTTG CCCTGTTGGA ATCAGTGGGT GTGATGTAGT TTACTGGCTG 180
GCAAGACATC AAGTTTGTCA AAGCTAATTG GGAACCATGA TAGAGATTCA AATTCCTTAT 240
ATGGTTTTTA GGACTGGGGA AGTGTTAGAG GAAGATTACG ACACTGCTAC TCCATGCCAA 300
AACGTTACAC TACGGCTCTG CAGACTGAAG ATTGCCTCAC AAGCAGAAAT ATACTCTTTC 360
CAACAAACAC TGGTGGAATG AAAAGGACAT TGGATTCCTG CTTCCAGTTA CTGCTTGCCC 420
TTCCCTGACT TTGTGACCTG AGGCAAGTCC CCAAATCCCT CTGGGCCCCA GTATCCTCAT 480
TTTTCAAATG GAGGAGGGTT AGAATTAAGA TGCAATCATG CATCCAGTTG TTTTCCAAAG 540
CATTGTCCAG CTAGGGAAGT GGTAGCACGT GGTGACTGAG AGCTTCCCCG ATCCTTTTAG 600
ATCAAAGAAC ACTTCTATGC CTTTGTGCAA CTGGTGTGCT GTGGGTACAG GTACTTTTAC 660
ATCCTCTAGT TAGTGAGTGC AAAGTACTCT TGGAAGCTCC CAAGCACTCA AGGTTTCAAT 720
CTGCATTCTT CTCCTCTATA TGCACTTTAT ATTTCAGGTT TTATAGTTTG AGGATTTGAA 780
AGGTAAGAAA AGTGTGAGCT ACAGATTTTG GAAGAATCCA GGAGCTGAGC TCATAGCTAA 840
GAACATGTCA GGGGTGTTAA GCAGCTCTGA AGTATGTAAC AAAGGCCATT TAGGTCTCAG 900
GAGGCTGCCA CCAGAACACT 920
|
