| Tag | Content |
|---|
EnhancerAtlas ID | HS091-49547 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chrX:57181290-57184080 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chrX:57182946-57182959 | GAATCTTCTGGAA | - | 6.06 | | PRDM1 | MA0508.2 | chrX:57182425-57182435 | TCACTTTCAC | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGTGGTATTC CTTTTATGTA GTACTCTCCT CTTTTTCCTG GGGATGTGGC TTCCTGAGAG 60
CTGAACTGTA GTGATCGTTA TTTCTCTTCT GGGTCTAGCC ACCCAGCAGA GCTACCAGGC 120
TCCAGGTTGG TACTGGGGGT TGTCTTCCCA GAGTCCTGTG ATGTATACTA TCTTTACTAT 180
CTTCAGGTCT CTCATCCAGG GATACCAGCA CCTGCTGCTG TGGGGATGGC AGGAGAGTTA 240
AATGGACTCT GTGAGGGTCT TTAATTGTGG TTGTTTGATG CACTGGTTTT GTGCTGGTTG 300
GCCTCCTGCC ACGAGGTGAC ACTTTAAAGA GATATGGAGG ATCAGGTGGT AGGTGGGGCC 360
CTAGTGCTCC CAAGAGAATA TGCCCTTTGT CTTCAGCTAC CAAGGTGGGT AGGGAAGGAC 420
CATCTAGTGG GGCAGGGTTA GGTGTGTCTG AGGTGAGACT CTCCTTGGGT GGAGCTTGCT 480
GTGGCTGCTA TGGCAGATGG GGGTGTGATT CCCAGTCAAT GAGTTATTTT CCCAGGAGGA 540
TTATGGCTGC CTCTGCTTTG TCATGCAGGT TATCAAGGAA GTTGGGGAAG CTGGCAGTTA 600
GAGGCCTCAC CCAGCTCCCA CGCAACCAAA AAGGCTAGTC TCACTCCCAC CATGCCCCAA 660
TAGCACTGAG TTTGTTTCCA GGCAGTGGGG CGTGCTGGGC TGAGAACTTG CTCCAGGCTA 720
CTACTAGCCT TCAGGCTGAG AAAAAAGCAG GGCTCCCTGC CTTTGAGTCT GCACACGAGT 780
TTCACGTCAT CCCCCAAGTT CTGGCCAGGA GACTTTGGGT TCAGTTGGAA CTGTTACAAA 840
GTTCAGCTGG AGGTTTCCTT CTACTGTGAT CTTTTCCCAG TTCCTCTGGC TACTGTGATC 900
TTTTCCCAGT TCCTCTGGCA GCCCTCCTCA AGGAACACTG TGAGACAAGT CAGACATAGC 960
TTCCCTGGGG ACCCAGAGAG CCCACAGGGC TTTTCCTGCT TCTCCTCTAC CCCTGTATTT 1020
CACTCGGCTC TATAAATTTA CTCAGCTCAA GGCAAGGTGA AATCCTTCTC CCGTGATCTA 1080
GACCTTCAGG TTACTCTGTA AGGGTATGTG TTCAGGGGTA CATGATCCCC CTTTCTCACT 1140
TTCACAGTTT GGGCACTCAC AGTATTTGAG CTGTCTCCTG GGTCTTGCAG GAGCAATTCA 1200
CTTCCTTCTC ATATTTCATT CTTTTTCATC CTCTGGTAGT GTGTTTTGAC ATATCACGTC 1260
TTTGAGCTTA CTAATTCTTT CTTCTGTTTG ATCAACTCTG TTATTGACAC ACATGCATTT 1320
TTCATTCTGT CAATTGAATT TTTCAGCTCT AAGATATCTG TTTGATGTTT TAAAATGATT 1380
TCAGCTTCTA TGGTAAAATC TCTGATGGAA TTCTGAATAC CTTCTATGTG TTATCTTGCA 1440
GTTCATTGAG CTTCCACAAA ATAGCTATTT TGAATTCTGC CTCTGAGAGG TTCTATATCT 1500
CTGGCACTTC AGGATTGGTT TCTAGTGTCT TATTTAGTTC ATTTAGTGAT ATCATGTCTC 1560
CTGGATGTTC TTAATGCTTG TGGATATTCT TCAGTATCTG GGCATTGAAG AGTTATGTAT 1620
TTATTTCAGT CTTTGCAGTC TGGCCTTGTT CATACTGAAT CTTCTGGAAA TGGTTTTCCA 1680
AGAATTCAGA GGATACAGTA TTAAGTGACC TAAGCCTGTG GTGACTGTAG CGATTTCAGC 1740
ACTAGGTGGC AGCCTGAGCC CTGGTATGCT GCAACTCTTG CATTCTCCTA GATACACAGC 1800
CTTTGTGGAC TTGGAAAAGA TAAGAGAGAA TTCCCTGGTT TTCCAAGCAA AGTCTCTTGC 1860
TCTGTTACCT CTCTTTCTGC TAATCAGATG GAATCTCTCT GTGCTGGGCT GCCTGGAGTT 1920
GGGGGAGAGG TGACACAGGC ACTCCTATGA CCACTGCACC TGTCACCGTG CTGGGTTGCA 1980
CTTGAAGCCC AGGGCTTTCC AGACCGACAC TAGTACTGGA CCTCACCAAA GGCCCACAGC 2040
TGCCACTGTT TGGCTACTGC TAATGTTTAT TCAGTGTCCA AATACATTTT AGTCTGTAGA 2100
TGGCGAATCC AGCCAGAACT TGTTCTATCC CACCAGGGCA GCAGATTGCC TTCTTCGTCA 2160
GGGTGGGTTT AATAATGATG TACAGGAACA AAATTCTGGA ATTGGAAGCT TCAGTATTTG 2220
ATCTGGTGCT TTATTTTACT GTGGCTGAGC TGATACCCAG TTGCAAGACC AAGTCCCTTG 2280
TACTTTTATT TCTCCTTTGC CCAAGTGGAA AGAGTCTTTC TCTGAGCTGC ACTATGTGGA 2340
ATTGGGAGAG GGATCACACA GGTCCTCCAC ACCAACTGCA GCTGGTGTCC TGCTGAATCT 2400
CAATTCCATT CCACAGCATC TGAGACCAGC AGAATGCACC CAATGACTGT AGTCATGATG 2460
GCCTGGTTAC CACTCAAATT TTCGAGGCCC TGAGCTACTT TAGTCAGGCA ATGGCAAATT 2520
GGGCCAGGAC CTGGGTTTCT CCTACTGGAG TATCAGATTC CCTTCTGGTC CAGGGCTGGT 2580
CTAAATGCTC CCTCCATGGG CACCAGTAGA AGTCTGCCTG GTGTTGCATT CCACTGTGAC 2640
AAGGTGGCAC TGGGTTCCCA TGCAATCTCC ACACTGACTG CACTCTTTCT CTCCCAACAC 2700
ACAGATTCTT CTGGCTGCCC TGTTTTAGAT TGGGAGAGGG GTCATGTAGA CAATGTGAGA 2760
CTGTCCTTTC TATCCTCTTG AATGCATTTT 2790
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