| Tag | Content |
|---|
EnhancerAtlas ID | HS050-04698 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr1:168662330-168663540 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat4 | MA0518.1 | chr1:168663327-168663341 | TCCTTTCCTGGAAG | - | 6.84 |
| | | 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 |
| GH01I168693 | chr1 | 168662351 | 168663491 |
| Enhancer Sequence | AGAAACCAAT CTCTCTTTAG AGCAATATGA CTGTATGTTG GACCTCCCAG GCCCCCTTGG 60
TAAGGCCAGT ATTTCCTGGA GAACCTTTCT CAAATGCATA CCTTATTTTT TGCCTTCCAT 120
AATATCATTT CCATTGCCTT AAATTCTACC ATCCCCTTTC CTATCCTGAC CTCTCACCGC 180
CTTCTATTGA AATGCCGCCT GCCCTTGACT TATCAAACTG TACTGTCACG GTTTGTTTGC 240
TTGACTAACT CCTTTAGTTT ATAATTCTCC AGAATGCAGG AACTGTGCCT AGTAAAATGG 300
TTGGTATATA ATAAACACTT GATAATTTAT TGATTCAGTT ACTGAGCAAA TGTAAGTGGG 360
ACTTAAGTTT GCTTGATAAA TGTTTCCTAT TATTGACGTT TACTAAAATC CGGCTTACCT 420
AAGGAATTTT ATTTCCAATA TATACTGACA CTGTTTTCCT TCTCTGACTA CATTTATTGG 480
GTACTTATTA TATGCAAGAC ACTATGTGAT CTCATTTAAT TCTTACAGTA ACCCTGTGTT 540
GTAAGTACTA TATTTCTACA GGTAAGGAAA TAGAGTCTCA GGAAAGGTAG GTGACGTGGC 600
CAAGGTCATA AAGCTGGGAA GTGACAGGAC CATGATTTGT GTCCAGGAAG TCTGACGCCA 660
GAGCTTACAG TCTTTTCTAC TCACCTCAGA AGTCCTACTT GTCCTTCAGG GCCAAGCATA 720
GACTCGGCTT CCTCAGGAAA CTTTCTTGCA GTTATTGTCA TCATCTATCT TCTCATCTCA 780
CCATTAGGCT GAAGGCCTTG TGAGGCAGGA ATCATGTATC TCCTCTTTCT ATTATCTCAT 840
TGTATGTGGC CAGCATCTTG TAAAGTTGTT TAGAAAGGAA TTCCTACCTG TACTGGGCAG 900
ATGAGGGGAA GGGGGCTTGG GGATTTCTCT AATCTTACAC AGCCACCCTC TGTCAGAGCC 960
AGCGGTAGGC CCTAGGTTAT CATCTTTAGT TCCAGGCTCC TTTCCTGGAA GAAAATGCCT 1020
TAGAAAATCC CTTTATAAAC AATTCAGGAG GTGATAGAGT TCAGAGATTC TTAGAATTGC 1080
GAGAAACCAC AATGGTTACC TAGATAAATG TCCTCATTTT AAACAGTAGG CCTAGAAAGG 1140
AGAGGTGACT TATCCAAGAC TGTGGAGCAA GTTAGTAGAA AGTTTGGAGT AATGAAAAAA 1200
CAGAGAACAA 1210
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