| Tag | Content |
|---|
EnhancerAtlas ID | HS187-20092 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr5:139629010-139630490 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr5:139629920-139629935 | TGGCCTTTGCCCTTC | - | 6.35 | | INSM1 | MA0155.1 | chr5:139629551-139629563 | TGCCAGGGGGCA | + | 6.62 | | NR2C2 | MA0504.1 | chr5:139630394-139630409 | TGCCCTCTCACCCCC | - | 6.27 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_31400 | chr5:139628953-139630350 | Gastric | | SE_38338 | chr5:139629328-139634238 | HUVEC |
|
| | 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 |
| GH05I140250 | chr5 | 139629793 | 139634422 |
|
Enhancer Sequence | TGATCCTAGC TTATAAAGTT TTAAGGGCAG TTACCCAGGC CTCTGCAATT CAGTATGGTC 60
AGAGGCGTGG CAGGATTGGT CCTGTGAGTG CAGAAGAACC TTGGGAGGCC TCTGTCTCCA 120
CGGGTGTCTT AGTCTGTTTG TGTTGCTCTA AAGGAATACC TGAGGCTGGG TAATTTATGA 180
AGAAAAGAGG TTTGTTTGGC CCACAGGTCT GCAGGCTATA CAAGCATGGT GCAGCATCTG 240
CTTCTGGAGA GGGTTTCTGG CTGCTTGCAT TCGTGGTGGA AGGCGAAGGG GAGCCACCTG 300
TACAGAAATC ATGTGGCCAG AGAGGAAATG AGAGAGGAGG TGCCAGGCTC TTTTCAACAG 360
CCAGTCAGTG AAGAAACAAA GCATGAGAAC TCACTCCCAT GAGAATGGTA CCAAGCCATA 420
CACAAGAAAC CCGCCCCCAT AATCCAAACA TCTCCCACCA GGCCCCACCT TCAACACTGG 480
GGATCAAATT TTTTTGCGGG GGTTGGGGGG GTCTGGGGGT ACCAAATTTC AACATGAGAC 540
CTGCCAGGGG GCAAAGAAAC CCTATGCACA CCACAGCAGG GGCATCCTTC ATTTCCAGTG 600
CGGTGCTGTG CTCTTGGGTA AGGGCACTAA CCCCATTTAA AGGGCTCTGC CCTCATGACC 660
TACTCATCTC CCAAATGGCC ACACCTCCTA ACACCATCAT CTCAGGAGTT AGGATTTCAA 720
CAAAGACTTT AGGGAGAAAC AACTATTCAC ACCACAGTAC TTTTCAACTT CCAAGAAGCC 780
ATGCATGCAT GGTCTTGGTT TCAGCTAAAT CTCCGACCTC ACCTCCAACA ACTCTTCCCC 840
GTCACTCCTT CAGCTCCAGT CACACAGGCC TCCCATGCTG CTCCTCCAAT CCACCAGGTA 900
TGTTCCTGCC TGGCCTTTGC CCTTCGCTGT GCTCTCCATG TAGAAGTTCT CTTCCCCAGA 960
TATTCACATT ACTCATCCCC TCACTTCCTT CAGGGCTTTC TCAAATGTTA CCTTATCTGC 1020
GAGGCCTTCT TGAGTACATG CTGCCCAATA CTCCCTATTC TCCTCACCTT GACTCTTCTC 1080
CAGAGCTCTT TCCACCACAG GAAGGAGAAA CTGTCTGGCT TCCCTTATGA GACGGAAAGG 1140
TCCACAAGGG CAGGACTTTG TTCTGTCACC TGATACGGTC CTACCGTCTA GAAGAATGGC 1200
TGGCACATAA TAGGAATTTA ATGTTTGTTG AATAAAGTGC TTTAGTGTGG GAAATGACGC 1260
CTTACTGATG TACACACACT TTTTAGTTTT CCCTCCCAAC TTGAATAATC AAGGAACGCC 1320
CAACAGAAGA AGCAAAGGCA GAAAATGACC ATTTTCCTTC AAGGTGGTTT TCAGCTTTCG 1380
GCATTGCCCT CTCACCCCCT GCCCCTGGAT ATACACAGAT TTAAAACTCC AACCTATCAC 1440
TACAAACAAT GTCAAGTATT TGAGGTAATG AATATGTTAA 1480
|
