| Tag | Content |
|---|
EnhancerAtlas ID | HS101-25819 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr2:208665280-208667760 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr2:208665434-208665444 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr2:208665434-208665444 | GGCACGTGCC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr2:208667229-208667244 | CGAACTCTTGACCTC | - | 6.24 | | RREB1 | MA0073.1 | chr2:208665970-208665990 | CCCCACCCCGCCCCCCACCA | + | 6.57 | | SOX10 | MA0442.2 | chr2:208667460-208667471 | AAAACAAAGCA | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28346 | chr2:208665705-208666707 | Fetal_Intestine | | SE_28346 | chr2:208666989-208667805 | Fetal_Intestine |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH02I207800 | chr2 | 208665704 | 208666592 | | GH02I207802 | chr2 | 208666990 | 208667805 |
|
Enhancer Sequence | CAGCTACTAG GGAGGCTGAG GCAGGAGAAT CACTTGAACC CAGGAGGCAG AGGTTGCAGT 60
GAGCCGAGAT TGTGCCACTA CACTCCAGCC TGGTGACAGA GAGAGACCCT GTCTCAAAAA 120
AAAAAAAAAA AAAAAAAATA TTACCGGGCG TGGTGGCACG TGCCTGTAAA TCCCAGCTAC 180
TGGGGAGGCT GAGGCAGGAT AATCGCTTGA ACCTGGGAGG TAGAGGTTGC AGTGAGCCAA 240
GATCATGCCA TTGCACTCCA GCCTGGGTGA CGGAGCAAGA CTCTTATCTC AAAAAAAAAA 300
AAAAAAAAAA ATCTGAGATG GGGTCCAGCG ATCTGTGTTT CAACAAGCTC CCCCCAGCTG 360
ATTCTGATAC ACACTCAAGC TTGAGAAACA CTGGTTTAGA TGAAACAAGA TTCACCATGA 420
GTTGATAGTT GTTGAGGCTG GTGACAGGTA CATGGGGTGG GGAGTTCACA TGTGTTTTTG 480
AAATTTTCTA TAATAAAAAG TTAAAAGAAA TGATTAAGCA CATTGGAAGG GAGGAGTGTA 540
CATATAATGG GGGAAGGGTC ATTGCTGGAG GACCTCTGGA TATAGAGTGA GACAAAACAG 600
ATTCTTGTGC ATGCATCTGT GTTGCCTTTT GAATTAAACA TCCAGGATAA TGGTTGCATT 660
AGCTCCTGCC TTTAACAGGA AGCTCTGCTC CCCCACCCCG CCCCCCACCA ACCCCAGTTC 720
CTCAGGTTTC TCTTCATTTG GAGCCTAAGT TTTAACAGGA TTAGATCCTG GAGCCTCAAA 780
TCTCTTAGAG AAGCAGCGAT TTGAATTTTC AGCTTCCACC TGAAACTGTG TCACTGTAAA 840
ATATGCCACC CACTAGACCT GCTTTATCAG CTGCAGACAT GATGCAATTA ACTAATTTTC 900
TGCAACCTCT CACCACACAA GCCGTGGAAC TTCTAGTCCA TTGTGTGGCT CGTTTACTTA 960
GCAGATAGGG TCTAAGAGCC TGTAACTATT TACCTCCCTC TAGAGGGGCT GTCCCAGACA 1020
GGTGAATTCA TTAGTTGGTG TTTGTAAAGC AGCAGGAAAA CCAAAAAAGC ATTAGGCAAG 1080
TTTTTATTTT TATTTCTTTA TTTGGCCTGA ACGCCACTCA AGCGATGTCC TGTCCTGTCC 1140
TGCGTTGTCA GTTTGCCTCC CTTCATATCC ACCCCCTCTT CTCTCTAGCC CATTTTTCTC 1200
TTATTCAGAA ATGAGAGATG CCCACAACTG GAAAACTCTT CCCATTTTGT CCCAGAGGAT 1260
GCAAAGTTCT GCCTGCCCAT CACATGGGAT CAGCGATCTT TAGGTTTTTT CATTTAAATG 1320
CCAAGGCATC TCTGCTTCCT GTTTCAGGTG TCCTTCTGCC CCATCTTTGA GCAGTGGTCT 1380
TTTCTTTCTT TTCTTCTTTC CCCACTTCCA TTTTCTCTCC TCTCTCTTTT TTTTTTGAGA 1440
CAAAGTCTCG CTCTGTTGCC CAGGATGGAG TGCAATGGCA CCATCTCGGC TCATTGCAAC 1500
CTCCACCTCC TGGGTTCAAG TGATTCTCCT GCCTCAGCCT CCTGAGTAAC TGGGGTTACA 1560
GGCAGGCACC AAAACGCTAG GCTAATTTTT GTATTTTTAG TAGAGACAGG GCTTCACCAT 1620
GTTGGCCAGG CTGGTCTCGA GCCCCCCGAC CTCAGATGAT CCACCTGCCT CAGCCTCCCA 1680
AAGTGTTGGG ATTACAGGTG TGAGTCACCA CGCCCGGCCT CACTTGGTTG TTTTTTTTTT 1740
TTTTTTTGAG ACGGAGCTTC ACTCTTGTTG CCCAGGCTGG AGTTCAATGG CGCAATCTCG 1800
TCTCACTGCA ACCTCCACCT TCCAGGTTCA AGCAATTCTC CTGCCTCAGC CTCCCAAGTA 1860
GCTGGGATTA CAGGCATGTA CCACACCCCT GGCTAATTTT TTGTATTTTT AGTAGAGACA 1920
GTGTTTCACC ATTTTGGCCA GGCTGGTTTC GAACTCTTGA CCTCAGGTGA CCCACCCGCC 1980
TCAGCCTCCC AAAGTGCTGA GATTACAGGC ATGAGCCACT GAGCCCCAGC TCCCTTGTAT 2040
TTTTCATAGA AAAGGCACAA GGAAGAAGTT CAATGATGAG AAGGAAGAAA GAATATTCCT 2100
CAAGTGTAAT TAAAGGTAGG AAAAATGACA GTTCTTTTGG AATCCAAGTT TGAAAATATT 2160
TCTTTTTAAT GTGGTAGGAT AAAACAAAGC ATAACAGTAA ATTGACCGTT TAACCATTGT 2220
TAGGTGATAG TTCAGTGGCT AAGTACATTC ACACTGCTGT GCAACCGTCG TCATCAGCAC 2280
TTCCAGAACG TTTTCGTCAT CCCATACTGA ACTCTGTACT CATTAAACGT GGAATCCCCA 2340
TTTCCCCTCC CCACCCCTGG CAATCACCAC TCACTTTCTA TTACATCTCT GTGAATTTGA 2400
CTACTCTAGG TACCTCATAT AACTGGAAAC CTACAGTATT TGTTTTTTTG TGTCTAGCTT 2460
AGTTTAGCAT AATGTCTTCA 2480
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