| Tag | Content |
|---|
EnhancerAtlas ID | HS048-19598 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr2:2616880-2618210 | | | 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 |
| GH02I002613 | chr2 | 2616835 | 2618158 |
| Enhancer Sequence | TCTAAATATC TTTATTTTAG GTTCAGAAAT AGTTTTCAGA GGCCTGGTGT TCCTCTGGGT 60
CTTCTACCTG ATGGGCTCTT TTCCTTGTTC AGCAACGTCC TTTAGGTCCC ATGCTAGTTC 120
TTTTTATTCG TGTTGTTTTC CTTTTTGTGA GTTTTTATTT TGCTTTAACT CTTCTTCAGG 180
GAGAACTCAG TTGTCTAGGA CTAGTGCCTG CCAACTGCCG CGTGGTTACA TGAAGGAGCC 240
TTGGATAGAC TTGCTTCCCA GTCCTTAGCT AGAGTACAGC GTGATATGGA AGCGCCGGGC 300
TCAGCCTCTG ATTTAAGCCG CTCTGCGCAC TGAGGACACC GCCCCAAACC CCATGACTCT 360
ACCCAGAATG CAAGCAAGAT GGTGCCAGGG CGCACTAAAT CCCCAGCATG CACTGCGACC 420
GCCCTTAGTA GCAAGCGTAA ACTACAATCC CCAGGATGCA CTGCACCAGG GCTGCGCCTG 480
CCTGGCGTCA CGGGCGTGAA TTACAATCCC CAGCATGCAC CGGAGTAGCG GGCGTCATCA 540
ACAACCCCCT ACGTGCCGCG CGCGGCCTCT AGCCCTCACC TGTGCTCTGC TTGTTCTGTG 600
CATAAACAAG GGTCTATGAG GGTGCAGAGG GTGCTCTGAG GGGCGGGGGT GGGAGGGGCG 660
GTGGGAGAAG ACTATTCTGG CCACCAAAAC GGCAGCACCG CTGCAACAGA AAAGATGCCT 720
GCTTCTCTGG AGGGTAATGA CGATGCTCTG AAGCTGACTG TGCTGCTGCA GGCATGCAAA 780
TCCTCTGACA GTTTTAAAGA GAGCACAGCA CGCATTTTAA GACATGGCTC CACCAGCCTT 840
ATGGCAAGCG GAATTCTTAT ATAATGTGGC AATGTATGGA CAGTCAGTTT TTGTTTTAGG 900
GGGCGTCACA GATTGTGTTC ACTTTGCATC TAGAACAGCT AGCCAGTGTC ATTTCAATCT 960
CTGGACGCCT TTAATTTGGG ATGTGCGCAT ATGCATCTGT ACTCTTGTGC ATGTAAATCC 1020
AAGTGTGTGA GTGAGCACTT GCATTAAAAA AATAATAATA AAATAAATAA AGAGGGATTT 1080
CAAGATGGTG ACAGCAGAGA CTGAAGCCAA GCATAGGACC CTCCTGGCTG GGGCCCAGGT 1140
CAGTGACCAG GAGGTGGCTG TGGTGCACGA CAAGGGCTAC AAGTCCTTGT AAATGCAAGT 1200
GTGTGAGTAC CAGTGCTCAA ACATGTGCAT GTATGCATAT CCCCTTCTCC GGGAGAGAAT 1260
CTCCTCCCGG TGGTGACATT GTTTACAGAG AAGGTTTTTA CACTAGCTAG CTGAGAGGCT 1320
GTGACTACAT 1330
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