| Tag | Content |
|---|
EnhancerAtlas ID | HS176-03881 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr1:228996010-228997840 |
SNPs | | Number: 2 | 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 |
|
| | Number of super-enhancer constituents: 5 | 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_49948 | chr1:228997517-229000847 | RPMI-8402 | | SE_52925 | chr1:228994663-228998395 | Small_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I228859 | chr1 | 228994940 | 228998147 |
|
Enhancer Sequence | GGGCTAGAGT GCAATGGTAC GATGTCAGCT CACTGCAACC TCTGCCTCCC AGGTTCAAGC 60
GATTCTCCTG CCTCAGCCTC CTGAGTAGCT GAGATTATAG GCACATGCCA CTACACCTGG 120
CTGATTTTTG TATTTTTAGT AGAGATGAGG TTTCACCATG TTGGCCAATC TGGTCTTGAA 180
CTCCTGACCT CGTGATCCAC CCACCTCAGC CTCCCAAAGT GCTGGGATTA CAGGTGTGAG 240
CCACCACGCC CGACCTTTTC TTCTGTTTAT GCAGTGGCAT GGAGCAGTCC CTCTAAGAGG 300
GCTGACCCAG GTATGAGTCA TTCAGTCAGC CTGAGGGTCC AAGGGCTGCT CCATGGTGAG 360
GCAGACATCC AGAAGGGTCC AGAGGGAGAA TCTATGGCAA GAGACAGCAG TCTAGAGGGA 420
TGGAAGTGGT GGCAGAAAAG CTGGCTTTTA AAAGGCAAGT TTTTATTCTA GGCTGACTTT 480
CTCTTATGTA AAATGTAGAT TTGCTGAGTG CCAGTGAATT TATAATTTTA GAAACCCATC 540
AGGGAGTTTC TAGATGAGTT TCTAAGAAGT CTAAGAAATG TCCAGGAAGG CCCTTAGCCA 600
CCTCGTGGAA ATTGGGAGAG AAGAAATGTG TGCAGAGAAA AGAGGGATTT TTGATGCAGA 660
GAAAAAGAAC AGGTGTGTCC CGGCTGCTGG CTCTGAGTAA CCCGTCTAAT CTCACTGTAC 720
AGAACGTACC TGCACTTTAT ACTAACAATG AGTGCCATTC AGCGTGCCAT TTATGATGTT 780
CACAGTGGCC TTCCTTGGTG TGGTCCCTGA AGCCCTGCAA AGCAGGGACT GTGCGGTCTG 840
AACCAAACAG GGGCCCCTGG GAATAGGGTA GCGTGTTCTG ATACCTGAGC TGGTAGTAGA 900
GTCAGAGCAA GAACAAAAGC CCCAGCGAGC AATCTGGGTT CAACCCCTGT CACCTTAGCT 960
CACGTGCCTG CATTGTGAAG TTCACGGTAA TAGCTTGACT GCATTCTCGC CATGGTTCTG 1020
GGTCAATAAA TCAGTCAGTA AGCACTGGGT GAGTAAGTAG TGCAGAGCAA AGTCTGAGCT 1080
TGGTGCCACA AGTGGATAAA AAAGAAATAG ATGACTCAAC CTCTGCTTAT AGGGAGGCTC 1140
TGATCTAGCT GAGATAGCAC AGAAATATTT GGAGAATGAC TCTAGTGCAG AACTGAAGGT 1200
GCAGAATGAC TCTGAAACGT TGCTGCACAG CAGGGTCCAA GAAAGGAGAG GGCAGTGCCA 1260
GCTGGGTATG CCAGGAAGGC TTTTGGGAGA AAAATACTGG CCAGGGTCTG GGAGAATCAG 1320
CAAACATGCC TGAGGGTAGA AAACCAGTGT CCCAGGACAG GGACCCTGTG CAGCCCTGGG 1380
GTGGGCTGGG TGGGACCGAG CCGGCAGTGC CTGCAGGGAT GATGGGCACC AGAGCACAGC 1440
TCTCAGCCTA TGTGTCCCGG AGCTCTGGGC GCTCCCAGGT GTCCTCACTG CACCGTGGTA 1500
GCTCCTGTCT CATGGAGCCA CCTGTCCTAG CACAACAGCT CCAATCACTG CTATTAGAAC 1560
AGATCCAAGG GGCAGGCTGG GAGGGTGTTA GGTTCAAAAA GGAGCACTAT GTAGAAGCAA 1620
GAAAAGAGAT GAAAGTTTTG CTCCTATCTG CATCTGGCCA GAGAGCAGAC TTTGATTTGC 1680
AACACCGTGT GGTCTCTGCA GGATTACGAA AGGGAAGAGG GGGTGGGCGG AAGGCTCTCC 1740
TCCCCAGTGC ATCATTTTCA GTTTTGTCTT TTACTTTCAA AGAAAGCTGT CTTTCTGACA 1800
CTGCATTCTG CCCTTTCTGA CCCATGTCCC 1830
|
