| Tag | Content |
|---|
EnhancerAtlas ID | HS129-03765 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:228995960-228997500 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:228996186-228996201 | TGAACTCCTGACCTC | - | 6.22 | | RREB1 | MA0073.1 | chr1:228995967-228995987 | GGGGGTGGGGTGGGGTGTGG | - | 7.06 | | RREB1 | MA0073.1 | chr1:228995962-228995982 | TTTTGGGGGGTGGGGTGGGG | - | 7.13 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_23450 | chr1:228996189-228997694 | Colon_Crypt_1 | | SE_27943 | chr1:228995103-228998116 | Fetal_Intestine | | SE_28861 | chr1:228994670-228998359 | Fetal_Intestine_Large | | SE_52925 | chr1:228994663-228998395 | Small_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I228859 | chr1 | 228994940 | 228998147 |
|
Enhancer Sequence | TTTTTTGGGG GGTGGGGTGG GGTGTGGGAC AGAGTCTCAT TATGTCCCCT GGGCTAGAGT 60
GCAATGGTAC GATGTCAGCT CACTGCAACC TCTGCCTCCC AGGTTCAAGC GATTCTCCTG 120
CCTCAGCCTC CTGAGTAGCT GAGATTATAG GCACATGCCA CTACACCTGG CTGATTTTTG 180
TATTTTTAGT AGAGATGAGG TTTCACCATG TTGGCCAATC TGGTCTTGAA CTCCTGACCT 240
CGTGATCCAC CCACCTCAGC CTCCCAAAGT GCTGGGATTA CAGGTGTGAG CCACCACGCC 300
CGACCTTTTC TTCTGTTTAT GCAGTGGCAT GGAGCAGTCC CTCTAAGAGG GCTGACCCAG 360
GTATGAGTCA TTCAGTCAGC CTGAGGGTCC AAGGGCTGCT CCATGGTGAG GCAGACATCC 420
AGAAGGGTCC AGAGGGAGAA TCTATGGCAA GAGACAGCAG TCTAGAGGGA TGGAAGTGGT 480
GGCAGAAAAG CTGGCTTTTA AAAGGCAAGT TTTTATTCTA GGCTGACTTT CTCTTATGTA 540
AAATGTAGAT TTGCTGAGTG CCAGTGAATT TATAATTTTA GAAACCCATC AGGGAGTTTC 600
TAGATGAGTT TCTAAGAAGT CTAAGAAATG TCCAGGAAGG CCCTTAGCCA CCTCGTGGAA 660
ATTGGGAGAG AAGAAATGTG TGCAGAGAAA AGAGGGATTT TTGATGCAGA GAAAAAGAAC 720
AGGTGTGTCC CGGCTGCTGG CTCTGAGTAA CCCGTCTAAT CTCACTGTAC AGAACGTACC 780
TGCACTTTAT ACTAACAATG AGTGCCATTC AGCGTGCCAT TTATGATGTT CACAGTGGCC 840
TTCCTTGGTG TGGTCCCTGA AGCCCTGCAA AGCAGGGACT GTGCGGTCTG AACCAAACAG 900
GGGCCCCTGG GAATAGGGTA GCGTGTTCTG ATACCTGAGC TGGTAGTAGA GTCAGAGCAA 960
GAACAAAAGC CCCAGCGAGC AATCTGGGTT CAACCCCTGT CACCTTAGCT CACGTGCCTG 1020
CATTGTGAAG TTCACGGTAA TAGCTTGACT GCATTCTCGC CATGGTTCTG GGTCAATAAA 1080
TCAGTCAGTA AGCACTGGGT GAGTAAGTAG TGCAGAGCAA AGTCTGAGCT TGGTGCCACA 1140
AGTGGATAAA AAAGAAATAG ATGACTCAAC CTCTGCTTAT AGGGAGGCTC TGATCTAGCT 1200
GAGATAGCAC AGAAATATTT GGAGAATGAC TCTAGTGCAG AACTGAAGGT GCAGAATGAC 1260
TCTGAAACGT TGCTGCACAG CAGGGTCCAA GAAAGGAGAG GGCAGTGCCA GCTGGGTATG 1320
CCAGGAAGGC TTTTGGGAGA AAAATACTGG CCAGGGTCTG GGAGAATCAG CAAACATGCC 1380
TGAGGGTAGA AAACCAGTGT CCCAGGACAG GGACCCTGTG CAGCCCTGGG GTGGGCTGGG 1440
TGGGACCGAG CCGGCAGTGC CTGCAGGGAT GATGGGCACC AGAGCACAGC TCTCAGCCTA 1500
TGTGTCCCGG AGCTCTGGGC GCTCCCAGGT GTCCTCACTG 1540
|
