| Tag | Content |
|---|
EnhancerAtlas ID | HS078-00553 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr1:26083780-26085080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx3-2 | MA0122.3 | chr1:26084147-26084160 | ATTAAGTGGTTTG | - | 6.1 | | ZNF740 | MA0753.2 | chr1:26083993-26084006 | GGGGGGGGGGCAG | - | 6.33 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_33518 | chr1:26082402-26088335 | H2171 | | SE_65420 | chr1:26084850-26085520 | Pancreatic_islets |
|
| | 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 |
| GH01I025755 | chr1 | 26082403 | 26088335 |
|
Enhancer Sequence | GCAAGGAAGC AGAGTGCCCC TGGCAGAGCC AGTCGCTCAA CCTGCTCCAC ACTAACTACA 60
CCTCAGAGCG TCTACAAATG GGAGGAGGTC ACACCACCCT GCTCTGCCCC ACCTCTGTCC 120
ACCACAGCCT TCCTGCAGAC CCTGTGCCCT TGGTTGTCCT AAATATCCCA CAGGAAAGAT 180
AATCATGATA CATATGAGGA AACTGAGGCA CGGGGGGGGG GGGCAGCTTG CCCAGAACCA 240
CCCCCATTCT GCACCTTCTT TTCCTCTTTA TTCCCACAAA AGCCCAGGAA GGAGGAGGCA 300
TGAACCTAGG AGATGGAGGC TTCGCCTTCA CTGTGTCTTA CGGATGCAGG CACGGAGGCA 360
TGCGAGGATT AAGTGGTTTG CCCGAGGGCT CCAGCTGAGC GACACTTGAA CCTGCACCTT 420
CTGGCTCCAG ATCTCAGGGA GACTTTCAGT GAATGCTCCC GGAAAGGCAG TGTCCTTGTT 480
CCCTATCCTA TGATCAAAAG AGAAGCAAAC TGCACAGCAG TTAGCACAGG CTCTGGCATC 540
AGAGCCAGCT CTGGGTCCCA GCTCTTCAAA TTACTGTGTG ATCTCAGGCA GGGGACATCA 600
CTGTCCTGTG CCTTGTTTAC CGCGTTTGCA AAAGGGGCAG CTGTGAGGAT TAACCAGGAT 660
CCTGCCTCTG CATTCTTTGT CTTTGAAAGC ACACAGCTCC AGATGTGTGG TCACACCAGA 720
GCTCCCTGCC TGTCCTATGT AGGTTCCATG AAATTCCAGG CCGGGGCCAT TTCATGTCCT 780
TGGGCAGCAC TGACAGTGTG CTGGGAGAGG GAAAGAGCTA GGCGGGGACT CTGCTTTTCA 840
TTGGTCCCAT TTGCACCCGA ATCACAGCAC TGTTTATCCT CCACATGCAG AACCACCAAT 900
GGTTGTGAGC CATCCGGTGC CTTCAGCCAG AGGACAGCAA CCGGGTGTTC TGTGGGGTCT 960
TTGTGGCCCC TGATAGCATT ATCCACATCA TCTGTAAATT CAGCATAACT CTTGTACCAG 1020
GTCTCGAGCT CCCAAGTCTT ACAGGGGTTG CTTGATGATG GAGACAAAGA ATATTCCAAG 1080
TCAGACAGGC CTGGGTTCAA ATGAACTTCA GTGAGTCACT TTATCTCAGT GTCCTCATCA 1140
GGACATGGGG CCAGGGAGGA TTCACTGAAA TTGTACGGCG AAAGCTCCTG GTTCCATGCC 1200
TGTCACATAG TAGGTGCCCC CACCGAGCAG CTGCTGTTAC TGTCAGCAGA GGAGCCAGCC 1260
TGGCCAAAGG GGGGATGACG GGGGCTGCTT CTGTCTTTTC 1300
|
