| Tag | Content |
|---|
EnhancerAtlas ID | HS048-31373 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr6:27145050-27146540 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr6:27145944-27145964 | CCCCCCACCACACACATACA | + | 6.19 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 27145585 | 27145720 | | chr6 | 27145729 | 27146130 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH06I027176 | chr6 | 27143805 | 27146978 |
| Enhancer Sequence | AACTGAGCTA ACCGGCCTCC TTGGTGGGAG GGTCTTTTCT TATGTTTATT TAAATCATAC 60
CTGATCCATG CCCGCTGAAT TTTTTTTTTT TTGTAATAGA AGCGTTACTT TCCCTTTTAT 120
TAATAAAATA TATTTTTTTT TAAGAAAAGG AGAATTCCTC ACTGTAGGCA CAGGAAAACC 180
ATGCTGTTTC AGGGAAAACA ATCTCAAACC ACTGATTCTG ACTGGAGAAA ACTCAGATTC 240
AACGACCCCA AGCAGGGCTT CCTTCCCCTC ACCAGGTGAA GGACTCAGAA CAAACCAAAA 300
AGCAGCTCCA AGCTTGCGAT CGCGGCCAGT TCCTCACGGA ACCAACCGCA GAGCCGCCGC 360
AGGTTCGCAG GATCGGAGGG TTCGGAGGAC TCGGAGGGTG CGGATTCCTC TCTGCTCCTT 420
GAGACCATTC CAGCCAGGTG GGCTCTTAGG CCTGGGAACC TGGGAAAGTG CACTGTCTCG 480
CCTCCTGGCC TCGCGGTGGT TCCGCAGTCA CCAGGACCCG AAATTCACAG CTGTGCGTCC 540
TAAGCTTGCA GCTCCACAAA CGATAAAATC AGACTTGGCC CTGCAGTGCC GGGCACCGGG 600
CCCTTGGTGA TGCTCGAGTG CCGGGCTGGC ATCGGCGTAA ATGAAAGGAC CAGCGGGACG 660
GCTCCTTTCA AGAGTCTCTG ACTCCTTCCG TCCCGGGAAG ACCAAGACAC CCACATCTAA 720
GACAAGGGAA GTCACCATTA TCTACACCAA TGATAAACGC CGGTATCTGG GAGGAACTGA 780
GCCCAGGACC GGGTCAGGCA ACTCAGAGTG TTGGGACAAC TAAGTCCCTC TTCAAAGACT 840
CAACTTTCTT GTCATAAGTT GCAAAAGTTG TACGTCAATC CTGCCTGCCC CCCGCCCCCC 900
ACCACACACA TACACTCCTT TTTTTCGCAA ATCCAGGGTT TACCCTATTT GCCAAAGTTT 960
AAGTCTTAGC CAATCGGGAT CAGCTTAGAT TGTGCGGTCC AACCCCAGCC AATAGGGGAA 1020
GGACACAGAA ACAGGAACTG CGTTAGGATT AAAAACTCCT TACCTCCTTT GTTTGGTGTG 1080
CTCTTGCAAT TGTAACAGGC AAGGAGCACC CTTCTGCAGA AGTAAAGATG CCTTGCTGAG 1140
GAATTTTCTA AGTGAGGGTT TCTTTTGGCT ACACCAAGCA CTTGTTTCCA GTAAATCTTA 1200
GGGACTCGTC CGGGATCCCA TTCTCCTTCG GGAGGGGCTA GCGATTATCT TTCATGGGGA 1260
GACGCGTCCC ATTGCCTCGT GGTGGCCCCA GGAGCGGAGG ATCGAGTCCC GCCCGAAGTG 1320
ACGAATAAAT CCGGACTCTC AGCAACGCGG ACAGTAGGGA GGATCCTTAA GAATTCTGTG 1380
AGACCAGCTT GGTCAATACG GTGAAACTCC GTTTCTACTA AAAATACAAA AATTAACCGG 1440
GCGTGGTGGT GCGCGCCCTT AGTCCCAGCT ACTTGGGAGG CTGAGGCAGG 1490
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