| Tag | Content |
|---|
EnhancerAtlas ID | HS040-06274 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr11:34213840-34215540 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| INSM1 | MA0155.1 | chr11:34214613-34214625 | TGCCCCCAGGCA | - | 6.04 | | ZNF263 | MA0528.1 | chr11:34215434-34215455 | GCTTCTGCCCCTCCCTCCTCC | - | 6.83 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I034191 | chr11 | 34213531 | 34215570 |
|
Enhancer Sequence | AAGAAAACCC CCCAAATATG TTAACTCATT GGGTCCGCAT ACCTTACAGA TGATTAAGAG 60
CCTTGAAGAG GTTAAATGAC TGGTTGAAGG TTATAAAAAG TGGCAAGGTA GATCTCAAAT 120
GCACGCCTTT GAATAGCAGG GCCCTCCTCA GATGGGGCTA TTCTGGCTGG CTACGAAGTC 180
ATGACACCAG AGGTTTCTAG GCCCGACCCC CAATCAGAAC TCTGGGAAGG GTTCCACACT 240
CCTCCTGTTT TCATGTCCTG GATACCAGCA GGCTCCAAGC CTTCTGAGTG TGCCACCCTC 300
CACAGAGGCG GAGACGTGCT GTGCAGGGCT GGGGAGAACG AGGCAAGAGG CCAGGATCTG 360
AGGCTTAGCA AGCGGACCGC TCTGTGGACC AGTGGCCCTC TGCCATTCCC ACTCTCTCTG 420
CCTGGCCACT CCTCAAGGGT CTGGCTTCTT TGCTGCTGCT CACAGTAGAT GCAGTCTGGA 480
AGGGTGCCTG GGGGACCCCA AACCCTCCAG CAGCCCAGGT TCTGATGTGG AGAAATGGTC 540
ACCTCCTGTC GACCTCAGGC CCTCTGCACC TCTGACTGCA TGTCTCCCTC TGTCTCCTCT 600
ACTTGATGAC GCTGCCTTCC AGCAATTTGC TGGCAAGCGG GCGGCCCTCT TGCCTTCCTA 660
CGTGTCTGCG TAGTCTTTAT CCTTACTGCC CCAGACCTCT CATTCCCCAG AAGGGTGATG 720
GCTGAGGAGG TATATCCTCT GCCAAAGATT CTGTTCCAGC TAGCCCATCC CTCTGCCCCC 780
AGGCACAACC AGCAAGGGCC ACATCTAACC AGATGGTTGT CCTTTCTCCT CCAGACCTCA 840
GAGGAAGGAG GCTCCCGATC TCCCTGGGCA ACCTGGATCC CTGACAAGAG GCTCTTTCAC 900
TTTCTAAGCT TGATCTCCGG TGATGACACA CCCTGCAGGG CAGCAGCTGT GACTAATTCT 960
GTGTTTTAGA CTCTGCCTTG TGCCTGGCTG GTGCCTGGGA TGCAAAGCTG CCAGTGAGAA 1020
AGGCACCCTG GAAGGGTGCA GGGAGGCTCC AGCTGCAGAG CTTTCCCAGG ATAGTGAGGG 1080
GGTGGGGCTG GAATGGCCCC AGAGAAGGTG GCCCCAAAGG CCAGGGCCCA CCCAGCATGC 1140
CTCAGTGCTG TAGGATCAGG TCTCAGCAGC CAGCTGGGAA AGCCACAGCC TGGCACAGGG 1200
AAAGGCAAAG GCCTTGAGGT GAGAGAGACC TCAGGTTTGA ATCCTGGCCT CGCCACTTAT 1260
CAGCCAGGTA CCCCGCGGCC TCCTGTACTC ACTTGTGAAA CGGAGGTAAT GATAGCACCA 1320
AACTTGCTGA AGTTCTTTGG GCCTAGAAGT AGGTAGAAAT GGGCTTTAAA AGAAGGGCGT 1380
ATGTTATCTG ACTTTGTCCT ACCGGATAGA ATTACTTAGC CCCATTTTAC AGGTGAGGAG 1440
CCTAAGGCAT GGAAGGGCCC TCTGAGCCCA GGCCTCTGCC CCAAAGCCTG TACTGTTTCT 1500
TGATGCACCA GGCTCACTGC AGGAGTAGAT GAAAGGAGGT TAGAGGCTTC TCATTCCCTG 1560
CAAGGCTGCC CGCTCACCAC TCTGAGTTCC TGCTGCTTCT GCCCCTCCCT CCTCCCACTG 1620
TCTCTTCTCC CAAACCAGAG CAGAGAGCTC TGGGGAGAAG GCCCCTTACG GAAAGATGTG 1680
AAGTCCCCAC CAAACACTGC 1700
|
