| Tag | Content |
|---|
EnhancerAtlas ID | HS048-27756 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr4:57597680-57598950 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr4:57598865-57598882 | CGGCTCACTGTGACCTC | - | 6.01 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCAGCACATT TTGGTTCTCA GAGCCCTTCA TTTGGTAGCT TTCCTCTACG AATGTTCCCT 60
GAAACCCAGC CCAGATTATT TTTTATTTTC TTTTTTCCAT ACTTCTCTCT TAGCTCCTTA 120
TGATATAAAT TGACTTTGTC TTCTGGCTTC ATTCTTTAGT ATCCTGTTCA TGTAGCCCCT 180
TTTTATACAC AAAAGGGTGA TCCTAGAATT GACCCAAGCC ACCAGGAATT TTACCCCTTG 240
TCCTCCTAAC TCTCAAGTCT GCCTTCTCTA TGTCTATTTC TGTATCATAA GAAAAACAGA 300
GAACCAGCAA AGACAGAATT CTCTTTGGAG AGTAGGGAAG AGGGAGAAGC TGAGCAAATT 360
AGGAGAACTT CTCTTTAGCT GCTGGGGATG GAGGAGAGAA AAGACGGTCG AATGGGAACA 420
CATAGCTAAT TATCCTTGTC TTTGTCACAT TCCCAGAGAT GCATGACTGA GGTGCTATGT 480
CCTTATCATT GCAGACAGGG GGCCAGGCAG AGTGGGGCTG ACCCAACAGC ACAGAGGGCC 540
TTGGGCGTGG CAGGGAAGCT TACTTCTGCA ATCCAGCTCA GCCTGGTGTT TCCTCTGAAG 600
CAGCGAACGG GGGGGGGGAA AGCTCATGGA GGGCCGGGGA GGGTGGCAGA TGCCTCCAGC 660
TCTCCAAGCC CTGCTGCCAG CCTCAGACCC AGGATCCACG CTTTGCTTCC AAGCCCGGAG 720
TCTGTTCACA GAAAGGCTGT GAGAGCCACT CCAGGAAAGA TTAGAGCCAC ACTTCACTTT 780
CTCTCAAGGT AAAACAAGGG AACAGACTTT TAAATCCTGG ATGTGATGGC CACCTCAGCA 840
AAGCATCTCC ATAGGCCCTC TATCCATTCC TGCTGCCCAC AGTCATTCAT AATTTCTGCC 900
CAGACTCACT TCAACTGTCC ATGAAGTCAC CCCCAACTTT CCACCTCTCT CCAGTCTCGG 960
TCCAGGTCAC ATGCCACTGT CAGTCTAATC TTCCCAAATA CCAGTCTGAT CACACCATTT 1020
CCCCACTCAA AATTCCTCAG TTACTCCCCT TTCCCTGTAA GTTCCTTGCC TAGACCTCAA 1080
AAGCCTCGAA GCTCCCTTTC TACACATGTT TTTCTTTTCT TCTTCTTCTT TTTTTTTTTT 1140
TGAGACAGTC TCCGTCACCC AGGCTGGAGT GCAATGGCCT GATCTCGGCT CACTGTGACC 1200
TCTGCCTCCT AGGTTCAAGC AATTCTCCTG CCTCCGCCTT CTGAGGAGCT GGTACTACAG 1260
GCATATGCAG 1270
|
| |
|
|
|
