| Tag | Content |
|---|
EnhancerAtlas ID | HS180-44119 | Organism | Homo sapiens | Tissue/cell | Small_intestine | Coordinate | chr7:7453950-7455290 | | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 7454152 | 7454202 | | chr7 | 7454264 | 7455086 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH07I007414 | chr7 | 7453790 | 7457050 |
| Enhancer Sequence | GGCCTGTGAC ATGAACCTGA AAGTCCAAGG CCATTTTAGG ATCAAACAGC CACAGTCCCA 60
TATTCATTGA TCCAAACAAC AGACATCTGT GGTTGGGAAA AAGCCCAAGG CCCTGAAGGA 120
GCTGGAGTTC CACTTCAGGG CAGAGCCAGT TGGGCCAGCA GAGGAATGGC AGGAGGCTGC 180
CATGGTACTA AATAAAGAGG GGCGAGCCCA TCGTGCTCTC AGGGTTTTCC AGGACCAGAG 240
CTACCACAGC AGCAGCCCTG GGTGGTCCCA GAGCCCCAGG AAAGGCCGGG GAAAGAAGTT 300
CCCAGAAGAT CATACTCTTC CACATAGAGA ATCAAGAGAA TAGGAAGGGG CATGGAAAGA 360
GAAGCCCTTC TACTCCCACA TTCCTTCCAG TCATGTCCAT TCATTCTACA AATGGTAGCC 420
AGAGTGAGTC TCTTCCAAAC TGATCAGATC ATTCTTCTCT GACTTCCAGT TGCTCCTAGG 480
ATTAAGGCCA AACTCATTAC TTGGCCTATA GGACCTCACA AGGGCCCTGC CTACTGCTGT 540
AATCTAAATT CACTCCATTG TGCCATCCTC TATACTCTCC AGAACTCAAA GTTTAATTAT 600
TTTATAGCCT GTAAATTCCA TGAGGACTAA GTTCACATAT TTTTACTCAC TACTTTATAC 660
TAGCACTTGG CTTATTTGCC TGACATAGGT GATGCTCAAT CCGTATTGGT TGGTCAGCTG 720
AATGAATGAA TGACTGGCTG AAGAGCCAAT ATTCTAGCAA CTAAGTTAGG TTGAAGCAAA 780
TCACTTGTGA TTGCAGCTAC AACCCTTATT TCTCCCATAA GTGGAAGGGG ATAGAGAGAC 840
AGAGTACAGT TCAGGCTTCT GTGTTAAAGG TTAACAGCAA CAAAGCTTTC CGTCAAAGGC 900
TACTAAGCAC ACACACCTGC AAGCAGATTT CACTGATTCA AATGCTCTTT GGAAAGGGGT 960
AGGAAATAAG TCAACAAATG AATGTAAGAA ATGAAATTTT ACTGTTCCTA TATCCTTGAA 1020
ATGACTCAGA AGAATGCCAC CAATTTGGTT TTTCAGTTCC CTCCCTTTTG CAGTGATGGT 1080
ATTTCGTCGG TGCAAAAGTA ATTGCGGTTT TTGCCACAGT CAGGAAAATG AGATGGAAGT 1140
CCTGAGGGAC GAACCTCTGC CCTGCTACCA ACTGGATGCC AGGCAATCCA ATATGTCTAA 1200
AGAGGTTTTT CTGGTTGTTT TGTTTGTTTT TTGAGACAGA GTCTAACTCT GTTGCCCAGG 1260
CAGGAGTGCA GTGGTGCGAT CTTGGCTCAC TGCAACCTCC GCCTCCAGGA TTCAAGCGAT 1320
TCTCCTGCCT CAGCCTCCTG 1340
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