| Tag | Content |
|---|
EnhancerAtlas ID | HS048-03170 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr1:204770420-204773060 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr1:204772927-204772948 | CCTAGCACCCTGGTCAGCTCC | + | 6.58 |
| | | 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 |
| GH01I204801 | chr1 | 204770824 | 204772846 |
| Enhancer Sequence | CAGAGTTCTC TATAGAAGGT ACTTAAGGAC GATCCTTGGA GGGGGCTAGG GATCTTTTCT 60
TAAAGCTTTA TTGCATAGCA AGCACTTTGT TCTCATATAC AGTGGTGTGC TGGTAAATGT 120
TGAGCAACCT GCTGGGGGAT GGGGAGAATG ATTTGTAGTG TGTGCCAGTT TCCTTAGTGT 180
GGAGGCTCCC TTCATGGCCA ATTTCATGCT ACCAATGTGA AATCTGAAAG CAGCATTGAG 240
AACAGATGCA CACAATCAGC TCTGGCACAC CACTGAATTA TGCTTATTGG GGTGGGGGGC 300
TTTGAAGGGA TTGATGGAGA TTATGGGGCT CTAAAGCACC CCCAAGCTTC TCCTTAGTGC 360
TGCCTCTGGG CTATCCTACT CTGGAGACAC AGAGAGGATT GAGCCTGGCC TCCTCCCTGG 420
GCCATGTTTG GGGACTGTGC TCTAGGTCAC CTGCTGACCC CTGCAGATGA GCACGGAGTC 480
CCAGCCTTGG TACTCTCCAG AACCCGTGCT CCCAATCAGG GTGTCAGATC TGGTGAGGTT 540
CCTTCCAGGC CCCCGTACTG TCCACACACG GCACAGTGCC TCTCATGCAT CTTCAAAACA 600
CTCTGCAGCA GGTGGCCAGG GTGAGCGAGA TGTCCCTGCA GACAGCATTT GTGACATTGA 660
CAATGTTTGT GGTATGTGGG TTGATTGGAC AGGCAGTTGC CTCATAAAGA AAAGAGAGTT 720
GGTCTTGGAG CCAAGAACTT GAATTTGAAT CCCAGTTCTG CTGCTTATGG CTCTGGAACT 780
ACAGATAAGG CAGGTCACTA TTCTAAGCCT CATTCTCCTC CTGTGGGAGT TGAGGAAATG 840
GGTGGTATTA ACCCCTGGAC ATTGTGGAGG GCAGAATGAG ATGGCATCTA TGAAAGCATC 900
TGCTTGGTGC TGGGTACGTA GAGCTTGAGT TCTGGGTCTT CATGTTTAGT TAACTATAAT 960
CCATGGTGAC ATTTACATCC CACCGAGTCA CAGAGTCACA GAATCTGGGC ATTGGGGTGG 1020
GCTGAAGGGG TTGTAGATTT CTTCTTCCCA CCCTATTAAG AACTCCTTTT ACAGTATCCC 1080
TGATGGTGGC CACCTTGTCT GTGCTTGATT AAGTCTAGAG GTTGAAGTTG GCTACATCTT 1140
GGAGACCCAG ACAGCACTCA GGGTTAGAAA GTTCTTCCTT TCTCTGTGTC CATCAGCAGG 1200
CCTTCCCCTG CATACTCACA TATACTCTGA CACACGTCAG TAGGAGCATA AATATTTATG 1260
ACATGTAGCT AATGCAGTCG GCTTATAGGA TTCCCAGAGC TTCAGATGGG AGATTTTTGC 1320
ACGAGAAGCC CTTTATCTGG GGAGGGGTTC TGGATGGGGT AGCGGCAGAT GCAGGCTCAG 1380
AGATGCTCCT CTTGGCTTCT CTGAGTGTTC TGGAAGCCTG CCCTTCACTG CGGCAGCCCA 1440
AGTGTCTGAA TTTGCAAGGA AGGTTAGCTG GCAGCTGCCA CTGTGGGCTC TGAGCACTGA 1500
GAATCAGCCA GCCTTCGGAA GCTTTCACTC AAGAAGCCCC TCCTGGGCTC TGCAGGACCA 1560
GGCCTCAGGA GGATGGATCC CCGGTCAGAG GGTCTAAAGT GCTTCTCACC CTGGCCTCCT 1620
TGAGGCGGAG CCCTTTGAGA GGGTAGAGCA AAGGGCACTT ACACTCACCC TCACTGGCTT 1680
CTAGATTTCC TCCAGAGCTG ATTGCCGGAA GGAAGTCTTA GATGACTGCC TCTAACCCTC 1740
AAAAGGGCCC CTGGTAAAGT CACCCCAGCA CATAGCCCAC ACACCAGGAA CTGCAAATAT 1800
TACAAAGACT TCAAATAGTG TAGCTCAGGG TTCATCCACA CATAGGGTCA GTTCCTCCCA 1860
TGGCTGGCTG GTCAGTGCCC ACCATGTGGC TGTATCATCC TCTAGACTTG GGGGTGGGGC 1920
TGGGGGTGAG GAGTGGTGGG CAAAGGAGTG AGAGAGCTGG ACTCCCTGGA GAGCAATCAG 1980
GCTTGGGCAT GAGGGTGCTC CTGCCCAGTG GGATCTTTTC TGGGGAGCAT CAGCAGGGTA 2040
GAGCTCGGGC TAGCCTGGCC ATTGGAGCCT GTGCCCAGCC TGATCTGGAG AGGGAACTGG 2100
AGAGGAGAGT GCTCCCTGGA AGGGAGGAGA ATGGCTTCCA GCTGGACTCT TGATGAGGCA 2160
GGATTTAGTC ACCCCAGAGC CCCACTTCCA ATCCTCTCCA AACCTGCACG CTGAACTGCT 2220
ACCTCTCCCT TCAGGGTCTT ACACTCTGCA CATCTATTTT ACCAGGATCT AAACTCATTC 2280
CTTTTGCACC TTTGATGAAA CCGGTCTCCT TTCTCCGACC TTGGACAGCT AGGCTGAGAA 2340
AAGGGAGAGA GCAGAGTATC CAGGCTGAAA AAGACTAGCT GTGTGAGCTG GACTGGGAGC 2400
CCCAGGCTCT CATTCACCTT TAAACCTGAG CCAGAGAACC ATCTCCTCCA GAAAGTCCCT 2460
CATCCCCCCA CCCACAAAAC CAGTGCAATT CCCCCACCCT CTGTTCTCCT AGCACCCTGG 2520
TCAGCTCCCG ATCGATCACT GCTAACAACA TTGCATTAAT TTTGTTCATG TGACTGTTTT 2580
CTCCAAAAGA CTGTAAGCTC TTTAAGAGCA GCATCTGCAC ACTGTTTGTC TATCTTTGAA 2640
|
| |
|
|
|
