Tag | Content |
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EnhancerAtlas ID | HS098-40217 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:139166200-139167570 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TCF3 | MA0522.2 | chr3:139166588-139166598 | AGCAGGTGTT | - | 6.02 | ZNF263 | MA0528.1 | chr3:139166937-139166958 | TCTTCTTCCTCATTCTCCCCT | - | 6.04 | ZNF263 | MA0528.1 | chr3:139166924-139166945 | CCTTCCTCCTTTCTCTTCTTC | - | 6.06 | ZNF263 | MA0528.1 | chr3:139166748-139166769 | TCCTCTCTCTTTCTCTCCTCT | - | 6.19 | ZNF263 | MA0528.1 | chr3:139166764-139166785 | CCTCTCCCTTCCTCTTCCCTC | - | 6.1 | ZNF263 | MA0528.1 | chr3:139166908-139166929 | CATTCTCTCCTCTCCTCCTTC | - | 6.23 | ZNF263 | MA0528.1 | chr3:139166664-139166685 | CTCTCCTCTTCTTTCTTCTTC | - | 6.25 | ZNF263 | MA0528.1 | chr3:139166661-139166682 | TCCCTCTCCTCTTCTTTCTTC | - | 6.35 | ZNF263 | MA0528.1 | chr3:139166646-139166667 | CTTTCTCCCTCCTCTTCCCTC | - | 6.37 | ZNF263 | MA0528.1 | chr3:139166928-139166949 | CCTCCTTTCTCTTCTTCCTCA | - | 6.45 | ZNF263 | MA0528.1 | chr3:139166934-139166955 | TTCTCTTCTTCCTCATTCTCC | - | 6.46 | ZNF263 | MA0528.1 | chr3:139166655-139166676 | TCCTCTTCCCTCTCCTCTTCT | - | 6.51 | ZNF263 | MA0528.1 | chr3:139166761-139166782 | TCTCCTCTCCCTTCCTCTTCC | - | 6.58 | ZNF263 | MA0528.1 | chr3:139166931-139166952 | CCTTTCTCTTCTTCCTCATTC | - | 6.7 | ZNF263 | MA0528.1 | chr3:139166810-139166831 | TCCTACCCTTTCCCCTCCTTT | - | 6 | ZNF263 | MA0528.1 | chr3:139166842-139166863 | TCCTCCTCTACCCCCTCATCC | - | 7.35 | ZNF263 | MA0528.1 | chr3:139166915-139166936 | TCCTCTCCTCCTTCCTCCTTT | - | 7.66 | ZNF263 | MA0528.1 | chr3:139166652-139166673 | CCCTCCTCTTCCCTCTCCTCT | - | 7.68 | ZNF263 | MA0528.1 | chr3:139166912-139166933 | CTCTCCTCTCCTCCTTCCTCC | - | 7.92 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_28469 | chr3:139167035-139171033 | Fetal_Intestine |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I139447 | chr3 | 139166613 | 139167725 |
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Enhancer Sequence | GTTCAAATTC TGCCTCTGCT ACTTACCAAA TATGGGACTT TGAGTATTTC ACCTGGTCTG 60 AATGGGCACC TACATCCTAG TCCTGGAAAC AGCTCAAATA GGGACAGAGG AGGTGCTTAA 120 CAAAGGATTA AGCCTACAAC CTGGATCTAT TCCTTGCCTT GAAGACCAGT TGAGGGCCCA 180 GGATGAGCCT CCTGTGGGTG CACTAGCTCT GCTTTAATTG CCTAGTTCTA AAATGAATCT 240 TCCTTTGCAT TGGAGAAAAA AACAACAGAG GCTACAGAAA GCCCCTGGGG TCTGTCTCAG 300 CTGCTATTGC TCTGACTGTG GTCTGTGAAC CCTGGGTAGG CAAGACATAG CTCCCACCTG 360 TTCCTCTTTT CATCTCTTGC TGGTGAGGAG CAGGTGTTCT TTCCAAGCTT CTCCTATCTC 420 TCTCCCCTCT TCTTACTTGT TCCAGTCTTT CTCCCTCCTC TTCCCTCTCC TCTTCTTTCT 480 TCTTCCTTTG CCTTATCCTC TTCCCTGCTT TCCTCTCTCC CATTCTTTCC CCCTCCTCTG 540 CTCTTTTCTC CTCTCTCTTT CTCTCCTCTC CCTTCCTCTT CCCTCTGCCT TCCTCTTCAC 600 TTCCCTTTCC TCCTACCCTT TCCCCTCCTT TCCCATCTTC TCTCCTCCTC TACCCCCTCA 660 TCCCTTCCTC TTCACCTCTC CCCTCTGTTT CCCTTCCTCT CCCTGCAACA TTCTCTCCTC 720 TCCTCCTTCC TCCTTTCTCT TCTTCCTCAT TCTCCCCTCC TGTCCCTTCT GTAGCTCCCC 780 TTATCCCTTG TGGCATCAGC ATCTCCCAGC CTCAAAACTG GCAGTCACTG TTTCATCAGC 840 TCTGGCCCCA GCCAAAACCT CCCTCCCTTC TCAGCCAGCA GCAGCTGCTG GACTCTTGAA 900 GGGGGTAACA ATTAGTCATT GGAGGGTGGC AGTGGTTGAG GGAGACAGAG CGTGCCAGCC 960 TTTGCAGTCA TTGCTCTGTC ACCTCATGTA CAACAGGCTT AACTCAACAC GTGATCTTCC 1020 CTTTGGCACC CCCCTCTCCC TCTGCCACTG CTGAGCTGTG TTGTGTGTAT TTGTCCTCCC 1080 TCGTCCCCAC ACCCACAACC ATCTTTATGC CCTCACCTCC TCTGTGAGCT TTATGCAGCC 1140 CTGCCTAGTG TGGCAGCTCC TTAAAGCACC TCTCTTGTTC TTCCCTTCCT TCCTGTGACC 1200 ACTCCCTATC CCTAATATGG GTCCCTCACT GCTTCTCCCC TGAAATACTT GATCCTGGGT 1260 TCCTCTCCCC ACCTTCATCT GTCCTGTCAA CAATGACTGG AGTGCATTCC TGGTTCATGT 1320 CCTCCTAGGG ATGAAAAAGA GTGACATCTT TCCTCCCCAC CACACTCCTA 1370
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