| Tag | Content |
|---|
EnhancerAtlas ID | HS040-03232 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:209830820-209832140 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NEUROG2 | MA0669.1 | chr1:209831768-209831778 | GACATATGTT | - | 6.02 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_27998 | chr1:209830223-209832731 | Fetal_Intestine | | SE_28741 | chr1:209814195-209833833 | Fetal_Intestine_Large | | SE_34999 | chr1:209830313-209831651 | HeLa | | SE_35828 | chr1:209818955-209834822 | HMEC | | SE_64514 | chr1:209821496-209832464 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CAGCCCAGTA CAGCCTACAG CCTGGTGGAG CCATATGCTG GCCCATGGCT GGCTGGCTCC 60
CAGAGAAGAC AGAAGAATCT TTTCATTCTT ACCACCTCCA TCCCCTCCCA TATTTCCTGA 120
CATTCCTCTG GCAGACAGGC TGGCCCATCG CCACACCCCC TCCTCTAACC CCAGTCACCT 180
CTGTCTCTAT TCTGTGATTC TATTTGGTCA TTGACCTCTG GGGATTAGGT TATTGGGATC 240
TAAGTCCGAC CTTTATGACC TTTGGATAAC ATTTGCCATG TGTAGTTGGC CATGTGGCCA 300
TGGTCCAGCC TCCATGAGAG GAGAGAGACA TACAGCTGTC TGAAGGGGCA CATAGCCACG 360
TGGCATGGTG GGTCTGACAG GTCGGGAGCT TCTGGGGAAG AAGAAGGGAA AGCAATGGCT 420
GAGAGCGAGC TGGGGCTTTT GTGTCCTGAA ATCTGCTCTT GAAGCTCTCA CAGGGCTGCC 480
CCACAGGACT TTCAAATTCT AAATATGATC CCTGAAAGGG CTACTAGACA GACAAACTAA 540
GTGTCCTAAC ACGTAGTTTA AATTGGCATT AGTTTAAATT GGCATTTGAT GGCTGAGTAT 600
GGAGAAATAA GCACCTTGTG GTTTGATGGG GAAGAGAGAA TGGGTGCGTC TGGCTTCTTG 660
TCTGGAATCA ACACCACCTA AGGGCTTTTA ATCAGCACCT GCCCACAGCG CCTGTGGCTA 720
CACCGGGGTA TGTGTATGGA CTTGACCGTA GCTCTGCTCT GCTACTCAAT AGAATTGTAA 780
ACTTGGGCAA AATCCTCTCT GAACCTCTGT TTCATTATTT ATAATTAAAG GTATTAGATT 840
CTAATGGTTC TTACTCAGGC TGCCCCTCAG AATTACTTGG AGAACATAAT ATATCACATA 900
CCAAGACCAG GCCTCACCCA GAGAATTATT CACTGGCAGA CGGGCAGAGA CATATGTTTT 960
TCAAGCTCCC TAGATGATTC TAATGTGCAG CCAGGGTTGG GAAACACTGA AGCCCCCTCC 1020
AGCTATAAGA TGCTGTGCCC TCAGGGTGGG GTGGTGCAGG ACAGTTGTTA AAAGCCTAGA 1080
CTTGAGAGAT GAAGGCTCAA GTCCTGGTTC TGCACTCACT ATCTGTGTGA CTTTGGACAG 1140
CTCGTTTAAT CTCCGATAGT CCCATTCCTG CAATGGGAAT AATGACAAAT CTACCTCATG 1200
GATACTGTGA AGATTAAAAG AAACATGCAT AATTGTCAGC AAAGTGCCTG GCTAGGGCCA 1260
TGCTCTACAA AGGGTGTCTG ACCCCATGTG TGCTTCACAC ACAGGTATTG GGGGCTATGA 1320
|
