| Tag | Content |
|---|
EnhancerAtlas ID | HS048-00827 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:29197140-29199410 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:29197995-29198010 | GAGGTCAGGAGTTCA | + | 6.22 | | TFAP2C | MA0524.2 | chr1:29198826-29198838 | TGCCTCAGGGCA | + | 6.18 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 29197193 | 29197303 | | chr1 | 29197696 | 29197746 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I028871 | chr1 | 29197683 | 29199480 |
|
Enhancer Sequence | ACATGTGCTG GAAAGCAGTT CTTAAGAGGA CATCTTTTCC CAAGCTCCTT AGCCTTAGCT 60
GTCCTCTCCT GCCCTCACCA GGACTGCCCT CTCAGGGACC CAAGAGGAAG GGACAGCCTG 120
GAAAGGAAGA AGGTCCCGGG CCATCTGCGT CATGGGGATG GAGTCCCTTG GCGTGTGCCG 180
GTGCAAATAC ACTCCTGTAA CGGGGCTCAT CTAGAATCTC CTCTCGGAAT GAGGAGACCG 240
CAAATGTGGT TTTGAATCTT CATTGTCCAC TTCATTGCTG TGGTGTTGGG CAGGTCTCTG 300
TCCCTCTCTG GGCCTCTGCA CGATGGAGGG GTAGGAGTTG ATGGTTCTGA AGGCTCTGCC 360
ATCCTGGAAA AGAACTGAGA CACTTCCCTC ATGTTCCTGG GTCCCAGAAA CAGACATCTG 420
TTGGTAAAAT CTACTGGGCA TTTGCCCAGA GACAGGGAAA AGAATGCCTG GGGGTCTGTA 480
ATAGGAGCTG CCCCAATTAG GGGCAGGGAG GCGGGCATGT AAAAAAGGAA GCTTAAAGCT 540
TTGTTTTCAG GCTTTTTGCC TACCCCAGGC TCCATCTTGG TACCAAGTAC TCAACCTTCT 600
GTTTTCTCAA TAAAGTGAGC CCTCTTCTCG GTGTCTGCAT CTCTGGCTGT TTTGTTTGCT 660
TACCTCTGCC AGGTTCCCTT GTAAGGGGCC CCCAGTCTGG GGGATCACAT AAGCCTATGG 720
GGAAGTCTGG CTCTGCCCTG AGGATGTGTC TCAGAGGGAG AGGCAATGTT GTCCTTAAGA 780
ACCCTAGTTT GGACCAGGTG TGGTGGCTCA CGCCTGTAAT CCCAGCACTT TGGGAGGCTG 840
AGGCGGGTGG ATCACGAGGT CAGGAGTTCA AGACCAGCCT GGCCAAGATG GTGAAACCCC 900
GTCTCTACTA AAAATACAAA AATTAGCCGG GCATGGTGGT GGGTGCTTGT AATCCCGCCT 960
ACTCAGGAGG CTAAGGCAGA GAATAGCTTG AACCCGGGAG GCGGAGGTTG CAGTGAACCG 1020
AGATTGCGCC ATTGCACTCC AGCCTGGGCG ACAAAATGAG ACTGTCTAAA AAAAAAAAAA 1080
AAAAGGCTCT AGTTTAATGG GAGAGACAGA CACACAGGCA GGCATTTCCT AGAGCGAGCT 1140
CTGAACCAAA CCAGGCCTCG GTGCTCCATT CCCCTTCCAC CCTCTGAACT GGCGCCTCCC 1200
CTTCCCTGCA GCCCTCCCCC CCGCCACTCC CCTAATCTAA GTCCCTTGTT CTCCAGAGCC 1260
CTCCCCACCC CACATGCCTC TTGGGGCTCC ACTAAATCTC TCTCCCATCT CTCTGCCCCT 1320
CAGTGACCCT TCCTTCAGGC CATAGAAGCA CCAGACCTCC TTGTGTGCAT TCAAGTTGGC 1380
CCTGGGGTGG GAGTTAGAAC CCCGTTCCCC AGGAGACTTC TGCCTCCTCA GTGTTCTCAA 1440
ATAGTCGCTG GCCCCTGTGG TTAATAAGTA ACTCCCTGGA AGGCAATTCT TTCCTGACCC 1500
AGATCTGTTT CCCATCACAT GTGACCCATC CTTAGGAGGC CACCAGAGCC TGGAGCCTCC 1560
CCCAGCCCTG GGGCAACTTC CCTTCAAAGT CCTCAACCCA GGGCCACTCA CCTTCGGGCC 1620
TGTTCATGTC AAGGTGATGA GCACCAAGGC AGATGGGCAG CCCTGATGCA GACTGGGATC 1680
TCAGCATGCC TCAGGGCAGG CTGTGTGGGC AGGGCCAGGG CGACCAGGCT GCCCGGGGGT 1740
AGGAGTTGGG GTGGCTTCTT GGCCCCACTC TGCTCATAGA GAGAGACTCA GTCAGGAAGA 1800
CTTCACAGAG GCCTGACAGA TCTAGTCAGA GCCAACTCCC ACCAAAGCTG GGAAGGACAG 1860
CTGTGAAGGT GAGAGAGAGA GAGAGTGTGT GTGTATGTGT GTGTGTATGT GTGTGTGAGC 1920
ACACAGCATG AGTGAGAGCA TCTCGGTGTT GATGTGAATG TATACAGAGA TTTTTTTTTT 1980
TTTGAGAGGG AGTCTTGCTC TGTCGTCCAG GCTGGAGTGC AGTGGCGCCA TCTCATCTCA 2040
CCACAACCTC CAACTGTTGG GTTCAAGAGA TTCTCCTGCT CCACCTCCCT AGTAGCTGGG 2100
ATTACAGGCA CTCGCCACCA TGCCCGGCTA GTTTTTGTAT TTTTAGTAGA GACTGGGGTC 2160
TCACCATGTT GGCCAGGCTG GTCTCGAACT CCTGACCTCA AGTGATCCAC CTGCCTTGGC 2220
CTCCCAAAGT GCTGGGTTAC AGGTGAGAGC CACTGCGCCC CGCCTATCCA 2270
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