| Tag | Content |
|---|
EnhancerAtlas ID | HS144-00227 |
Organism | Homo sapiens |
Tissue/cell | NH-A |
Coordinate | chr1:29472040-29473420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELK4 | MA0076.2 | chr1:29473398-29473409 | GCCGGAAGTGG | - | 6.62 | | ZBTB7A | MA0750.2 | chr1:29473397-29473410 | AGCCGGAAGTGGT | + | 6.01 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_00764 | chr1:29472186-29473874 | Adipose_Nuclei | | SE_28354 | chr1:29471733-29473943 | Fetal_Intestine | | SE_29089 | chr1:29471622-29474018 | Fetal_Intestine_Large |
|
| | 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 |
| GH01I029144 | chr1 | 29471501 | 29474791 |
|
Enhancer Sequence | TGAGATCGTG CCACTGCACT CCAGCCTGGT GACAGTGCCA GACTCCATCT CAAAACAAAA 60
CAAACAAAAA AAACCTGAAA GAAACAAAAT GCCGCAACAA ACATCCCTAT CCTTATAGGG 120
ATAAAATCGG AATAATAAAT TATCGTCATC ACTGGAGACC AGCATGAGAT CCTCTGAGGC 180
AGTGGGAATT TTACTGGTTA GGTTCATCAC CTTGTCATGA TGACACGAGA ATGGGCCCAG 240
AAAAAGGTTT GGGAAACTCT CCAGAAACTG AGTGAGGTTC CTTGGTTTGG CTGCCTCGTC 300
TGTTTCTGAA ATTACACGTT TTCAAAACTC AACTAATTTC CCCTGTCATC TTCCCCATTC 360
CTCAGATGAT GCCTCATCAT TCTGTGACTG CTTCCGATAG CTCCTTTGCC AGGACATTTG 420
CCAAGTCTTG CTAATCTTGC CTCTTCTGCT CCCTCCTATC ATGGCTTTGA TCAAGCAGGC 480
CCCGTATCAT CTGGGGTTGC ATGCCCTGAA CTATTGGGTT CCCTGCATCC AATCCTTCAC 540
AATGCTGTCA GGTCTAGAAG CATAACCCTA CTCCCCGCAC CCTCCTATTC AAATACCTTC 600
AATGTTACCC AGTGCTTACA GGATAAAGGT CAAATTCCTC TTCCTGGTAT CCATGGCCCT 660
CTATGACACA ATCCATTTTG TTAAACTCTA ACTCTCCAGT ATCAAACTCC ACGTTTCCTG 720
GGCACAGTAC CCTGTGCTTT CCCAACTCCA TGAAAGCCAT GCTCACAGGC TTTCAATAGG 780
AATGCGTCCC ACCCTACATC CCCAAAAGGT TCAGCTTAAG TGCTACCTCT GATCCCAGAT 840
GAAGTTCTGA CTCTGTTCTC TGAATATCCA CTTTGCCTTC ATCACTAGCA ACTAGATCAC 900
AAACTCCAGG AGGGCAAGAG ACACTCTACT TTCGTATTTC CAATGCATTC GAAGATTTTG 960
GTCTATAGGA AGCAACAGGA CAGTTGTTTT AAGCCTAGGG ACAGCCCCCA ACAAATTCAC 1020
AGGCAGCAGT CAAGTGAATC TCCTTTCCCA AGATTTTGCT GCAGCATGTA ATGAAAGCCC 1080
TCAAGCATCC TCCCTGCTGT GATGCCCCTC AACAGTCCCT CAAGGGCTGA GACCAGATTG 1140
GAACCACTGT ACTTCTGGTA CCTCCTAGAG AGCTAGGCCA AACAAGCAGT GGAAGAATAA 1200
TTAGGACAAA AGTTATCCAG TAGGCCAGGC GCGGTGGCTC ATGTCCGTAA TCCCAACACT 1260
TTGGGAGGCT GAGGTGGGCA GATCACCTCA GGTCAGGAGT TCGAGACCAG CCTGACCAAT 1320
ATGATGAAAC CCCGTCTCTA CTAAAAATAC AAAAATTAGC CGGAAGTGGT GGCATGTACC 1380
|
