| Tag | Content |
|---|
EnhancerAtlas ID | HS040-18333 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr19:33867010-33868360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU2F2 | MA0507.1 | chr19:33868159-33868172 | CTCATTTGCATGT | + | 6.54 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_24617 | chr19:33867463-33868359 | Colon_Crypt_2 | | SE_25205 | chr19:33867347-33869467 | Colon_Crypt_3 | | SE_27838 | chr19:33863654-33869944 | Fetal_Intestine | | SE_28702 | chr19:33863718-33870174 | Fetal_Intestine_Large | | SE_36697 | chr19:33863666-33869285 | HMEC | | SE_52890 | chr19:33863704-33869433 | Small_Intestine | | SE_64786 | chr19:33863644-33868991 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TAAACAGAGT TAGGACCAAG GAGAAACATC TGTGACTATT TTGAAATGTT GACCTTCATT 60
GAGGAAATCG AGTGAAAAAT TTATTTTGGT GGGCAAGGGG AGGAATATTG GGTTCTAGGT 120
CTGTGGAGAA AAGGGACAAA AGGGTTAGGA AAATTCTTGA TAGGTTTATT TTCCCAGGTG 180
AAACTTGAGA AAAATTTGAT TTTGTTTTAC TCATTCTAAC ATTCTGCGCT TTCAGTGTGA 240
CTGACGTGAA TGAACATTAC TTGAATTAAG TTTGAATTAA AACAAAGCCT ATTACCCACT 300
TAGTCCACCA TTCTCAATAT TCATTGGGAA TCAGCAGCAG AGGCCCTCAG ACTTCAGTGT 360
ATTCAGAGTT ACTTGGAGGT CTCCTTATGA AAAGATTACT CAGCTCTGTT CTTAGAACTC 420
CTGATTCTAA GTCTGGGGCA GCCTGAGAAG TTACATTTCT AAAGAGTTCC TGGATGATGA 480
TGATGCTGGT CCAGGGACCA CACTTTGAGA ACCACTGCTC TTCAGCTTTC CTGCTGTTTC 540
CTCCTTGAGT GATTCACATG GAAGGAAGCC AGGCGCCGCC CTGCATCCTG TAGCCTGAAC 600
TTTGGAATAG TGTTTGTCCA CAGAGGAGCC AGACTTGAAT TTAGGACTGA GTGTCCAGCT 660
TTCAAATAAA CACTTTTTGC CTGTTGTAGG TGTTCAGTAA ATGTGTGTGG AGGAACAAAG 720
CGTAAATGAG AGTGGCCTTT TCAGTGTAAA ATCACTTAGC TCTTTGATCC CCTTTTACTT 780
GGTTAATCTT CACTTTAAGA GCTATTTATA TGGTTAAAGA ACTTACTAAA CAAAACATTC 840
TTGGAGTTAT TTTGATTATC TCCAAGTTTC TCTTTCTTAC ATTTTCACCA GTTTGTAGGT 900
TCAGTGAATA CTCTTTTCAG GCCAAAGGGC TTACCTTTAA AACCTCACCT ACCACACACG 960
TTCAGCCTAG TACCTTGCAA GATGAGTCAG GCAGAGGTGA AAAAGCCCTT CCCTGTTCCT 1020
GTATCTTTGG ATACGGAAAC AGGCGTGAAC GTTGCTGAAC GTGGACCCTG TAGTGAGTAA 1080
GAGCTGTTTG TTAGTGACTG AAGGTCGTGG TGTGTTGTCT GTAGGAAAGT GTCTTACTAT 1140
TCCACATCCC TCATTTGCAT GTGGGGAACA GACAGCCATG GAAGAAAAGA GATTTGCCCA 1200
AACTAAAATA GGGGGAGCCA CAGCCAAGAC AAGAACTGGC CTGGTCACTG GTCTCTACCG 1260
CTTTGGATCA TTGCTATCTC TGAGCATGGA CAAGTTGACT GTAGAGAGCT TTAAAGGCTA 1320
AAAATATAAT TGGTATATTA AAAAAAAAGT 1350
|
