| Tag | Content |
|---|
EnhancerAtlas ID | HS048-22222 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr2:228270330-228272000 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr2:228270609-228270624 | AAAGTCAATAGGTCA | + | 6.67 |
| | | 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 |
| GH02I227404 | chr2 | 228269316 | 228273140 |
| Enhancer Sequence | ACTTGGGTCA GTGACTGTGG GAGCTTCAGA TTCAGGAGTT TGGTGGACTG TGCCAGAAAC 60
ACGCCTTGCA CCTGCTTACA GGGATGGAGG AGCGAGGACT GAGGGGGGCC AGAGATCCAA 120
AGTTCTTGTA TCTCCATAAG AAGGTGTAGG AGCAAGCCGA GCAGTCTGAA ATTGTCATTA 180
AGAACAGAAA ACCTGCAGAT GGGCATATTT ACACACATGG CTTATGTGGG TGTGGGTGTG 240
TGGATGGGCA ACATCAAAGA GGATATGAAT GGTGATTCAA AAGTCAATAG GTCAAATATG 300
AAAATGCTAG GAGGACATCT TCATGTATCT ACTGTATAGT CCAACTTTCG GTTTATGGAA 360
AATGTCCAGC TCTTTTAGAA GGTAAACATT TTCTGACTGT GAGCTCTTGA ATATGAATTT 420
TATGGTACCT TATACATTTT TTAACTTTCA AAGCTCTGGG TTGGGTAGTT ACCAGTACCA 480
TCTTCACAAA TTCTGGATTC TTCTGGATGT TCTTGACTAT TCTGGGAAAA TTGGTGCGTT 540
TGTTCTCCCT CCGCCTTGTA CCGAGGTCTG CAGGCTTAAG GGATGTTAAC AAGGCTTCAA 600
TTTGCTGTGT GCATTAGCAG GTGCTGGAAA CTACGTTGCC AAATGTGTCG TAGACACAAG 660
AGGGCGATGT GTGCTCAAAT GTCAACCTCA CCGAGGAAAA GGAATTCATC CTTCAGGAAT 720
TTTTGGCTGA ATTCCCAGAC CTAAAAAAGA TTAACAAAGT GTGTTTGGGA GGGGCAAAAT 780
TCACTGTGAA ACCTAATCAA AGAGGCAGGA TGTGATGTCA GAGTGTGGAG ACAGCCTGGC 840
AGGAGCTTGG AGGGGATTCT TATCCTTGAG TTCAGAACTG GGCAGTACTC TAGGCTAATG 900
ATCGTTATAA TCAAGACTTG TCCTCTGTCT GGATATTCAG AAAAGACAGA CTTCAAGGCT 960
GCAGAGAATC AGTGGCTGTC TTGGTCTCTG ATTACAAAAA CTTTATTCTG AGAAAGCCCC 1020
TCATTCATTG GAGGAAAACT GGCTGTGCAC TTGTTACATG CCAGGCATGA GTCTTGTAGG 1080
GGCTAAGAAT TCAGCCTTGA GTAAGACAGC CGAGGCCACT GCCCTCTGGA AGCATCAGTG 1140
ACCCTTGGCA CGTACTCCCA TCTATTTGTT TCTTTTCTCT CTGAGCCAGT CCAAACCAGC 1200
AGTATCTACA TCATCTTTTC TTGTTCTGAA AGAGAATGCA AGTCACACAT TTATGGCTGT 1260
GGGCCACATT TTTTTAGAGA TGCCATCTGG TTCCAGTTTT TCTGACTGTT TGTGGAGAGT 1320
GGTGATTCCA ACAATCTTCT ACCAAATGTA AGGGGGTGAT AAAAGTGTTC AGTGTTTGCC 1380
ACAGAGATAT CTCTAGCTTG GCCTGATCTC AGTGCACTGC TTTTTGGGTT TACTCAACAA 1440
ATTGAACAAT GCTCAGCCCC TCTTCCATGG AACCTTCCCA ATCTCTTTAA CCAGGGTTAC 1500
ACTGCGACTC CTCTAAGTCT CTGTACATCA TAGCACTTTT GTGGGAGACC ACTGCTACTT 1560
CAAATCTCTG CCAATAGCAC CATGTTTCCT TTCGTTGCTA GCTTTTTAGA ATTCTAAAGC 1620
CTACTTGGCC ATTAGATTTT TTTTATTTTT TTTTTTTTGA GACAGGGTCT 1670
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