| Tag | Content |
|---|
EnhancerAtlas ID | HS048-19858 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr2:21293320-21294040 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| | | 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 |
| GH02I021069 | chr2 | 21292447 | 21294637 |
| Enhancer Sequence | ACTGGTTACT TTGCTACTCA AAGTACACAT TTCCTATGGT GGAAACTCCC TTGTTTACTT 60
ATTCTTCCTG ACCCAGGTTT AAAAGGCCTG CCTAACCATC TCAGTAGGCT TTTCCTAGCT 120
GATATCCTTC TGAGCTGTGG TAGAGAAAGG GGAAGCAGTG CCCTCATGGC TCCTGGATTT 180
ACAGTTCCTG AGGAAGAACT GACAAATAGA GGAAGACTTC CCTAATATCA AATGAAGCAG 240
AACCTTCTGG GCAGAAGGAA AACAGGTGAT GTTGCAATGA CAGGGCTCAC CTTTCCACCT 300
CGTGTTTGAT GAGGGTTTGA GAAAAGAGCC ACATTCTTTC CAAAAGTCAG GTCAGAAGCC 360
TTTCCACACT TTGGTTTCCC AATTCAGCAC CCGTAATGTC AAATAAAACG AAGGCCCTTG 420
CCCCAAGTGA AGTCATCAGC AAATATCTCT TTGCTTTCCG GGGGACTGTG TTCTCTCACA 480
ACATCTTTTG GAATTATCAC TTCATACTGA AACAAGGGTT TGATCTTTTC ATGAGATGTA 540
TGGTGATGAA ATTAAGGCCA GGGGCTCTGG GGACAGAAGA GAAGGCTGGC GCCACTCGTA 600
TGCCCTGGAG AAACAGTGAG ATGAAGAGCA CAGCCTCTAG AGCCAGAGTG TCTGGATCTA 660
AAATTGGCTC TGCCAACAAG CATGTAAGTC ACATAGCTTT TATATGTTTC ATATGAAAAT 720
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