| Tag | Content |
|---|
EnhancerAtlas ID | HS180-11351 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr12:51922320-51923900 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6 | MA0677.1 | chr12:51923542-51923556 | TGACCTTTGAGCCC | - | 6.41 | | Rxra | MA0512.2 | chr12:51923542-51923556 | TGACCTTTGAGCCC | - | 6.43 |
|
| | 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 |
| GH12I051528 | chr12 | 51921842 | 51924303 |
|
Enhancer Sequence | TGAGCAGAGC TGTTGCTGAG CTGAGATACA GAAATGATGC AGAGGAACAT AATCTGAGGT 60
GCTGGCTCTG CTGAGGGAGT CTCAGGGACT CTGGGACCTC TTGATCTGCC CTTGGGTGTT 120
TTCCTCTTGA ATTCCTGTTT CTGTCCTTAC TACTGCCCTT GCCTGCTTTT CAGACTTCAG 180
ACTGATCTGT CACTGGCTCA TCGAGTACCT GAGCTGAGCA TCAGTATATC CTGGGGAAAG 240
TCAGGCTTCA GTGAAAGCAA AGCTCCAGAA GTGTTAGCAG GAAAGCTCAA GAACATAGGG 300
GAGTGTGCTC ACAAAAGACA GGGCATTCCT GAGGACACAA GGCAAAGGAG GGCATGAGCC 360
TGGGATGGGA TGGGCATATG AGAGTAAGAA AGCACGAGAA CCAGGAGAGG TTCTGAGGGC 420
ATGGTGACAT CTGCTGCTCT CCCCAGGACA CACAGCCCGC AGAGCATCAG GAATGTGCCA 480
GGAGCTACAG GCAGGGGTTT GGCATGGTGG TGAGCTAATA TCTGCAGAAT GCTGGGAATG 540
GCATCCGGCA CATAGTAGGT GCCATGTAAG TATTTGATAC ATAAATATGG ATAGAGCATT 600
AAGGTTTTTC CTGGCTGCCC TTTATCTTGG AAGGCAGCCT TGCTCCAAGC AAATCTCCAG 660
TGCCTCAGAC AAGCCACAGG AATCTCCCAG GATCTGCTTG CTGAAGGTTC AAAGGGCAGA 720
GCTAATGACA GGGAAGAGGC TTTCTCTCCC GCACCTTCAT CATCTTCACT CCACAGTCAT 780
CTCTTCTTCC TGCTTGCCCT CAGAGTGGGT TGTTATCTCC AAGGAATCCT TCATATGCCA 840
AAGTCCAAGA ACTGACCTGT AACTAGACTA GACTAAACTT CCTGAGACAC GGACCATGTC 900
TGCCATGTCC ATTTTTGCAT TCCCCATAAA GCACCATATC TAGCACACAG TACGTGCTCA 960
TTAACCCTGT GAAATGAATA TATGACCCAA CCCTGAGGTA AGTTAGCCTG CAAGTATAAC 1020
TTAATTAGGC ACAATAATAT CTGGGGAGAA GTCAGACCAA TACCAACCAC ATAGATTAAT 1080
TACAGAACAG TCTCAGTTGG GGCCATGTTG AGAATCTGCT TACTGGTGTC TGCGCAGGAA 1140
AGGGTTAACG CAGCAGGTAT GGGTTGCTCA AACCTTGCAC ATTCCAAAGA AAGGACTGGG 1200
CCCTTGACTG GCTCCTGGGA GGTGACCTTT GAGCCCTTGG AAGATCCTGC CTGGTTGACT 1260
TTTTTTCTAT GCCCCAGGCC TTAGGCCACA CTATCAGTCT GACCAGTTTG TGCTAATAAA 1320
GTGATTTATG GTGAATGTCT GGTTTTGTAT GCCTAAGGCC CTGCCTGGGC TGTGCACCAA 1380
CAGTTTGACC TCTCAGTAGC GTGGGGAACT AGAGACTGAG TGGCTAAAAT AAGTCATGTG 1440
GGTACTGCCA CCACATAAAA CCCCTGGACA ACAAGGCTCA TCCCTGGTTG GTAATATTTT 1500
GCACGTGTTG TCATGCATAG TTTTTGGGGG AATTAACTGC ATTCCCGTCA GGCCCACTGG 1560
GAGAGGACAC CTAGAAGGTT 1580
|
