| Tag | Content |
|---|
EnhancerAtlas ID | HS129-30921 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr6:3013520-3014620 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFF | MA0495.3 | chr6:3013914-3013929 | GTGCTGACTCATCAG | - | 6.22 | | MAFF | MA0495.3 | chr6:3013914-3013929 | GTGCTGACTCATCAG | + | 6.3 | | NFE2L1 | MA0089.2 | chr6:3013913-3013928 | AGTGCTGACTCATCA | - | 6 | | NFYA | MA0060.3 | chr6:3014231-3014242 | TCTGATTGGTT | - | 6.62 | | NFYB | MA0502.1 | chr6:3014232-3014247 | CTGATTGGTTCAGAT | - | 6.81 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_10010 | chr6:3012114-3014720 | CD14 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I003013 | chr6 | 3013881 | 3014030 |
|
Enhancer Sequence | TGGGTAAAGA TATCCACGTA GCCAATATCA CTCACTCCAA ATCCCGACTG CCATGTAAAT 60
AGGAATGAAG GATATTTCCA TTATTCCAGT GGTCCAAGAA TCATCTGAAA CCTGCCAGTC 120
TTGTTGCTTC CCTTCTCTTC CCGTTCCTGC CCTGAGACAT TCTGGGGCTG CTTGAGAACC 180
ACATTTATCT GCACAAATGT TTATCAGGGT AAATCAGGCC AAATGCATCT CCTTAAATAT 240
CCTGCCTTAA ATATCCTGAT CATTAAGAGG AAAATCTCTG GTTTCTACCC TCTCAGTGGT 300
TGCTTCACCC CCAGCCCAGC CACCTTCCTG TATTTGTTCA CAAGGAGGTG ATGCCACTGC 360
AGAGTGAACT GGCCCAGCAA AATGCCCTCC AGGAGTGCTG ACTCATCAGG CCACTTCCCG 420
CCACTGCAAG GAAGATGTGC AGGCATGGCT GTGGCTGTGT AAACCTGGCA GCAGAGTACG 480
CACATGAGCT TTGAGGGAAT TGTTGGGTGA CAGAAATTCC TGTCCAACTA GAAGGAAAGG 540
GGAATCTATT ATAAGGGCTC TGGTCACTTG GGCCTCCTGG ATCCCAAGGA CAGAGCTGTA 600
GCTGCTCTCG TCCACAGATT CCCATCTGCT CCTTTCTGCC TCTTGGCTCT GTTCTCTCTC 660
ACTGCTTGCC AGGGACTGGA TCCCCTAGAT CCAGAATTTC CAACCAAGGG ATCTGATTGG 720
TTCAGATCAT TTCTGTTTTC CAACCCTGCT TGAGGATGCG GAGTGGGCAG GAGAACGAGA 780
GCACTGTTCG CATGAGTCCG CCATGTGAGG GCAAGGCAGG GGGTGAGCGG CATGTGACCA 840
CTTTCCAGAC AAAACCACCT TTCCAGAATG ATGAGGTTCC CAAGCCTTCA TAAAAGCAAC 900
CTGCATGTGC GGGAAGAGGG CTGCCTCATC CCTGCCCAGG CTTGCCTCTG CACACCCCTT 960
CCCGACACCA GCCCTTTCTT TACTCAGTGA CCTTGAGCTG CTAATCTGAC CAAAGTGCAG 1020
GACGTCCTTT GTCCTAATTA CAGGTGGGTG GACTCATAGT CCTCAGGCCT AGGTGACCAT 1080
GTGGTTTACC ATCTCCGTCT 1100
|
