| Tag | Content |
|---|
EnhancerAtlas ID | HS048-38820 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chrX:68782610-68784340 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF7L2 | MA0523.1 | chrX:68783896-68783910 | GAAGATCAAAGGCT | + | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATCCGAAGAC CCAAAGTTCT GCTGCTTACC AACTCTGTGA CATATTGAGC AGTTTATTAA 60
CCTCTCTGAG CCTCAGTGTG ATGATCTGTA AAATGGAGAT AGTGATTGTT TCCTCACAGG 120
ATGGTTGTGA GGATTAAGTG GCAGATAATG CATTTAAAAG CCATTTGTAA ATGATGATGC 180
CTGTAAAGCT ATAAAGAGTT ATTAGTATCA TTATCATCTT CATTATAGTT ACTATTATGC 240
CACCCAACTT GGCTTGAAAT TCCACCCATA AGAGATTTAT TTCAACAACA AGCAAACACC 300
TCTGGAAGAA TTCAAAGGAG GAGCTATCAG TCATTCAAGA GTTGGTACAG CCTAGTCTAG 360
GGCTTCTCAA CTCTGGCTGC TGTTAGAATC ACCTGTGAGA TTAAAAAAAA AAATGATGAC 420
CAGTTCCTGC CCCTAACAAA TTAAGTCAGA ATATCTAGAG GTGGAGGCCA GGCAGGGCTA 480
TTTTTTAAAG CTCCCAATTT GCAGCTGCAG TTGAAATTTA CTGGCAAAAT GGGTCCTGAA 540
GCCAGCCAGA CAGCCCTGGC ATTGAATTTC AGATTGAATT TTATCTTCTT CACTTACTAA 600
GTGTGTGACC TTGGAGCAAT TACACAATCT CTGCAAGCTT CACTTCCCTT ATCTTTGACA 660
TGGAAAGAAC AGTGGTACCT ATCATATGGC TGTGGTGAGG ATTAAATGTG TTAATACGTG 720
TAAACCACTC TAGCACAATG CCTGGCACAC AGTAAGTGCA TGAATTGTTA GTTGTTTTTG 780
TTATTTGTAG GCCCTGCACC AAGCCCACCC TCAGAAACAC CTCCTGATCT TAGCGGGAGG 840
GGAGAGAAGG TGCAGCATGG AGTCTGCCTT ATCACTGCTC TTGCTTGGAC TCTAATGCCA 900
GGCTCCCAGT GGTTGTCCTC TTTGCCCAGA TGTTCTAACA CCTTGGGCTT CGGTTGATGA 960
CATGTGACTT TCACAGCAGG CTCTCCTTAA TGAAAATTGG CTTCTCCTTG AGATCTCATA 1020
TATCTAAATC CACATCCAGG CCTACTGTGT GCTGTGTACT GCTCTGGATT GATGCTTGAA 1080
CCTTGGCTCT CAGGTCTTGG CAATTGGCCC AGATCCAATC TGCCCACTTT CACTTCAGCC 1140
TTGCCCTCTT GAGTCCCACC CAACCCAAGT CTTGCTTTTG AAGCATTTCT GACAAGAAAA 1200
ACTGCCAGAT TTGTACACTC TGCCTTTCTG AAAAAGGGAC AGAGATAAGA CAAATGACTC 1260
CAGATTTTTA CCTAATGGGG AAATAAGAAG ATCAAAGGCT TCTGTGTTCA CTCTGTATAA 1320
CCTACATTGG CAACAGAGAG TCAGCCAAAA CCCAAAATGC CTTAACAGGT TTTGTACTCT 1380
GTATTAGTTT CCTATGGCTA CTGTAACGAA TTACCACAAA CTTGGTGGCT TAAAGCAACA 1440
TACATTTATT TTCTCACAGT TAGGAATGCC TGAAGTCCAC AATCAGTTCC ACTAGGCCAA 1500
AATCAAGGTG TTGTCAGAGC CCTGCTCCCT CTGGAGGCTC TAGGAGAGAA TCTATTCCTT 1560
GCCTCTTCCA GCTTTGGGTG GCTGCCGGCA TTCCTTGGCT TGGGGCTGCA TCACTCTAAT 1620
CCGCATGGTT ACATTGCCTG CTCCTATTTT CTGTGTGTCA AAGTTCCCTG TGCCTTTCTT 1680
ATAAGGAAAC ATGTGATTGC ATATAGAACC TACCCAGAAA ATTCAGGATA 1730
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