| Tag | Content |
|---|
EnhancerAtlas ID | HS092-00243 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:9204980-9207360 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB1 | MA0018.3 | chr1:9205463-9205475 | AGTGACGTCACC | + | 6.22 | | CREB1 | MA0018.3 | chr1:9205463-9205475 | AGTGACGTCACC | - | 6.22 | | Gfi1b | MA0483.1 | chr1:9205720-9205731 | AGCTGTGATTT | - | 6.14 | | SOX10 | MA0442.2 | chr1:9206074-9206085 | TGCTTTGTTTT | - | 6.02 | | TEAD1 | MA0090.2 | chr1:9207052-9207062 | CACATTCCAT | + | 6.02 | | ZNF263 | MA0528.1 | chr1:9206343-9206364 | TTCTCCTTCTCCTCCTCCTCC | - | 10.09 | | ZNF263 | MA0528.1 | chr1:9206364-9206385 | TCCTCCTCCTCGTCCTCCTCC | - | 10.26 | | ZNF263 | MA0528.1 | chr1:9206346-9206367 | TCCTTCTCCTCCTCCTCCTCC | - | 10.48 | | ZNF263 | MA0528.1 | chr1:9206349-9206370 | TTCTCCTCCTCCTCCTCCTCC | - | 10.92 | | ZNF263 | MA0528.1 | chr1:9206352-9206373 | TCCTCCTCCTCCTCCTCCTCC | - | 12.34 | | ZNF263 | MA0528.1 | chr1:9206399-9206420 | TCCTCCTCCTCCTCTTCCTGC | - | 6.06 | | ZNF263 | MA0528.1 | chr1:9206370-9206391 | TCCTCGTCCTCCTCCTCCCCC | - | 6.41 | | ZNF263 | MA0528.1 | chr1:9206387-9206408 | CCCCCGCCCCCTTCCTCCTCC | - | 6.44 | | ZNF263 | MA0528.1 | chr1:9206384-9206405 | CTCCCCCCGCCCCCTTCCTCC | - | 6.54 | | ZNF263 | MA0528.1 | chr1:9206408-9206429 | TCCTCTTCCTGCTCCTTCCCC | - | 6.5 | | ZNF263 | MA0528.1 | chr1:9206358-9206379 | TCCTCCTCCTCCTCCTCGTCC | - | 6.92 | | ZNF263 | MA0528.1 | chr1:9206340-9206361 | CATTTCTCCTTCTCCTCCTCC | - | 7.16 | | ZNF263 | MA0528.1 | chr1:9206390-9206411 | CCGCCCCCTTCCTCCTCCTCC | - | 7.36 | | ZNF263 | MA0528.1 | chr1:9206396-9206417 | CCTTCCTCCTCCTCCTCTTCC | - | 8.17 | | ZNF263 | MA0528.1 | chr1:9206405-9206426 | TCCTCCTCTTCCTGCTCCTTC | - | 8.45 | | ZNF263 | MA0528.1 | chr1:9206355-9206376 | TCCTCCTCCTCCTCCTCCTCG | - | 8.54 | | ZNF263 | MA0528.1 | chr1:9206393-9206414 | CCCCCTTCCTCCTCCTCCTCT | - | 8.97 | | ZNF263 | MA0528.1 | chr1:9206367-9206388 | TCCTCCTCGTCCTCCTCCTCC | - | 9.24 | | ZNF263 | MA0528.1 | chr1:9206361-9206382 | TCCTCCTCCTCCTCGTCCTCC | - | 9.29 | | ZNF263 | MA0528.1 | chr1:9206402-9206423 | TCCTCCTCCTCTTCCTGCTCC | - | 9.54 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_01288 | chr1:9204907-9205661 | Adrenal_Gland | | SE_45801 | chr1:9204852-9206131 | Osteoblasts |
|
| | 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 |
| GH01I009145 | chr1 | 9205096 | 9205905 |
|
Enhancer Sequence | ATGGATACAA CTCACTAAAC CAGTAAGATC CCTTCCTACA TCCTGAGGAA CTACCTGTAG 60
GAGTTTCTGA CGGGGACCAG AGGCAGCCTG TACAGGGGGC CTGGGGCTCT CTATGTGTGT 120
GTGTCCCGGG GCAGCCCTGG GTTTGGTGAG AGGGAGGATT CTGATCTCAC TCAGCCCTAC 180
TCACTCCGGC CCTCTTGGGA AGTGGGTACC AAGCCCTGAT CCCACCCGGG CTGGTGCAGG 240
ATGGTGGCAT CCCCGTGGCC TGCAGCCGAG CCCTGTGGAA GGCCGCTGGG CAGAGACAGC 300
TCCTCCGTTC ACAGGACCCT CATCCAAAAA CCCTCACATA TTTCAACATA GCCGCACCCC 360
GAACGTGGAC CCCTCAGGCA CCGGGCCCTG TGTGGCCATC CAGGCTGCAC ACCCATGAAG 420
CCAGCTCTGC TGCTGGGGGA CAGCAGAGAG AGGAACAGGC AGGCCGAAAG GTGTCCAGGG 480
CACAGTGACG TCACCAGGAG CCACTGAGTC ATCAGGAGGG CCTTTCATCA GTCGGCTGCC 540
TGGTCTGATC TGAGCGAGGT GGAAGCTTCC AAGGCCAGAC ACGGGGAGAC TCTGTGAGGC 600
TCCCACATTG TTGATCATTT CTTCTCATCT CTCCTCTCCT GACCAGATTG CTCTCTAACC 660
AGATTCATTT CAGGAGTAAG TGACTGCCGG CCAAGAAAGA CAACCCCCTC AAGGTTACTA 720
ATTTAAAGAC AGATGGGATC AGCTGTGATT TCAGTCGCAG TTATGAAAAT TAGAGCCAGG 780
TGTGGTGGCT CATACCTGTA ATCTCAGCAC TTTGGGAGGC TGAGGTGGGA GAACTGCTTG 840
AGTCGAGGAG TTAGAGACCA GCCTGGGCAA CATAATGAGA CCCCTTGTCT TTAGAAAAAA 900
TGTAAACATT TGCCAAGTGT GATGGCGTAC ACCTGTAGTC CCAGCTACTT AGGAGGCTGA 960
GGTGGGAGGC TCGCCTGAGC CCAAGAGGTC AAGGTTGCAG TGAGCCATGA TCGCACACTG 1020
CACTTCAGCC TGGGCAACAG AGCAAGACCC TGTCTCAGGA AAAAAAAAAA GGAAAAGAAA 1080
ATTAGACTAA GACATGCTTT GTTTTGCAAT GGTGCAGCAT CAAGGGGTCC TGGCAGGGAA 1140
GAGGTGGCAC CAGCCTGCAC CACTGCTGCA GAAATACTCG GGAGTACACA AAGCACTTCT 1200
CGGCTGGAGT CCAGAGGCCT TCATATTTGG TAGTTTACTC TGATGTTTTC AGTTCCAACA 1260
GAGGAAGAGG AAGGGGCTGG TCCACAGTGG CCTCAGGTAA TGCTCAGCCT TGGGGGATGA 1320
TGAACACAAT GAGGGGCACT TGGCGTGAAG AGTGAGAGTC CATTTCTCCT TCTCCTCCTC 1380
CTCCTCCTCC TCCTCGTCCT CCTCCTCCCC CCGCCCCCTT CCTCCTCCTC CTCTTCCTGC 1440
TCCTTCCCCC TACCCTCCCC ACACGGGAGG TGTATCAGGT AGTGAGTTTC AGCCCGGCAC 1500
GGTGGCTCAT GCCTGTAATC CCAGCATTTT GGAAGGCTGA GCCAGGCGGT TCACTTGAGG 1560
CCAGGAGTTC GAGACAAGCC TGGGCAACAT GGTGAAACCC TGTCTCTACT ATTAACAAAG 1620
TTACAAAAAT TAGGCATGGT GGGGTGTGAC TGTAGTCCCA GCTACTCGGG AGGCTGAGGC 1680
AGGAGAATTG CTTGAACCCA GAAGGCGAAG ATTACAGTGA GTCTAGATCG TGCCACTCTA 1740
CTCCAGGCTG GGCGACGGAG ACTCTGTCTC AAAAAAATAT TATTTCTTGA GGTCAGGAAT 1800
TCAAGATCAG CCTGCCCAAC AAGGTGAAAC CCGGTCTCTA CTAAAAACAC AAAAAAATTA 1860
GCTGGACGTG GTGGCGCACA TCTGCAATCC CAGCTACTTA GGAGGCTGAG GCATGAGAAT 1920
CGCTTGAATC TGGGAGGCAG AGGTTGCAGT GAGCCGAGAT CACGCCACTG CACTCCAGCG 1980
AAACTCTATC TCGAACATAC ATACATACAG CAAGCTCTCA ATGGGGCCAG TGAGCTGTGA 2040
GCATGTTTCC TCTGCACGCT AAGCTCTTGA CTCACATTCC ATCAGGAAGT TGGGGTCATC 2100
TTGACCAGGG AAGGGCAGGC ATCTTGGTGG GGGGCCCCTG GACTGTACCT GGTAGTGCTG 2160
CTAGCAGAGG AATGGAAGCT GGGCAGCAAA AACCCCTGAT GCCCACTAGT CCTGAGCATC 2220
CCTGGAAGCA TCCTGCCAAG TGCAAGGCCC AGGGTAAGTG CTGAATTAAT ACTTGCATTT 2280
TGCCTGGATC CTCACCCCAC CCACCAATTT TAACCACGGA TCCTGATGAG AGCTAAGTAG 2340
AGTACCAAAG GTCATTTCCG TTTTTTTTTT TTTAATGTAT 2380
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