| Tag | Content |
|---|
EnhancerAtlas ID | HS098-14354 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:106106220-106108930 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr12:106107531-106107552 | GGCGATGTCCATGGTGCTTTG | - | 6.16 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_37822 | chr12:106105155-106111544 | HSMMtube |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I105712 | chr12 | 106106709 | 106108628 |
|
Enhancer Sequence | TGGAGTATTT TTCTTGATAA TCAGTGTCTT AAAAAACAAA TTTAAACACC TTTAGAGGAG 60
CAGTTATCAT CCAGTTCTTC AGGCCCCGCT AATCTCCATG GCTTTGATAC TCTTCCCATT 120
TGCACATTTT TCTTAATCTA CTGGCCCATA TATATTTTTG AGTCTACAGA CCCCAATGCA 180
GCCCAATTTT AGAAAGCACT TCATATTGTG GCCTAATGAT GGGAGGGAGG ACAGTTTCTT 240
CTAGTCTTTA AAACTAAGAA CAATCTGCCT ATATGGCAGC AGGATAAACA TTTGTGTGGT 300
TGGAAGAGGC TAATCAAATC TCAGTGATTT TGAAACTCCA CAATTTAAGA ATAATTCTTG 360
GCTGGGCACA GTGGCTCACA CCTGTAATCC AAGGCTAAAG GATCACTTGA GCCCAGGAGT 420
TTGAGACCAG CTTGGGCAAC ATAGTGAGAC CCTGTCTCTA CAAAAAACAA TTTTAAAAAA 480
TTAGCTAGGC ATGGTGGCAT GAGAACCCAT AGTCCCAGCT GCTCAGGAGG CTGAGGCAGG 540
AGGATTGCTT GAGCCTGGGA GGTTGAGGCT GTAGTGAGCT GTGATTGTGC CACTGCACTC 600
CAACCTGGAT GACAGAATGA GACCTCACCT CAAAAAAAAA AAAAGAATAA TTCCTTTGGA 660
GGAAGTGCCA TGGGGTTGGG GATATTCGGG GAAGCAGGGA CTAGTAAGGT CAGTTTCAGA 720
TATAAGTAGC ACCTTGAGGT CCAGAGATAA AGCCCCTGTG AATTTCTGAC CCAGGCAAAA 780
TATTGCAGTG TTGTCTGAAC CAGGTGGAAG ATGAGTCTTT ATTCCAACTA AGTGTGGCCC 840
TCAAATGAAC CCTCAGTGGT GTTAAAGCAA ACTAAATATG GCCTGAGAAG GACTCCATAG 900
TTCTATATTT GAATCCTTGT GATGAAATAT AACCTAGCTT AATAGTCAGA CAAAACTGAA 960
AAGCTAACTT AGTAGTATGC ACCTTTAACA ATAGCTGAGT GTTGGCCAAT CCCAGAGGCC 1020
ATACTTCAAC CACTCATAGA CTGCTGAGTT TTCAAACTGT GTTTAAATAA GGCAAACGCC 1080
AACCTATAAC CAAGCTCACT GTTTCTGTAC CTCACTTCCT ATTCCTGTAC GTCACTTTAC 1140
CCTTTTTGTC TATAGATTTA TTCTGACCAT AGGGCACCCT TAGAGACTCT GTGAATCTGC 1200
TGTGATTCTG CCCAATTTGC GAATCGTTCA TTGCTCAATT AAACTCCTTT AAATTTAGTT 1260
CAGCTGAAGT TTTTCTTTTA TCAGTGGGCT GGGCCTCTTT ACTGTGAATC AGGCGATGTC 1320
CATGGTGCTT TGTCACAGCA GTTCTTTTCT TCTCAAGCTA GCTCATGTTT TTCAGAGTTG 1380
GTTTTGGAAA ACATCAGACT TGCAGATAGG CAGGAGTGAC AATGAAGGTG TTCATTCCTG 1440
TACCCTTCCC CCATCATTTG CACATGACCC AAGCTGGTTC ATTTTCAGGA AGCAGGGGAC 1500
ATAGCAAAAA TAAATTCATG AATAAGGCTA ATTATGTTCA ATGACAAGGC TAGCACCAAG 1560
CTGTTTTTAA ACATAAATTC AGTCACTCAG ACCACACAAT TGAAACCCTC AGCAAAAGTG 1620
CAGAGAGTTC TCTGAAAGCT ACTCACAGCT GCTACAGTTC ATTCCAGCCC CTCCCGGAAA 1680
ATTCCAAACA GAGGACATAT GCCCTAGACA CTGCCTGCCC TGTATGTCCT GATGTTAATC 1740
CCCAGGGGAA AACTTGATTG GATTCAATGA CAAAGCTAGC ATCAAGCTGT TTTTAAATTA 1800
AACTTTCCTT GTTAAGGAAA AGGGAACTAT CTGTGGCCCA TGACTTTTGA ACTTAGAAAT 1860
ATCTATATGG CCCATTAAAA ATCAGCCTCA TTCATTTGTT TGTTTGTTGC GTTGCTTCAT 1920
TTTGCTTTGC TTTCTTATAT GTAGGGATAA CTTGAAGCAA CATTGGAAAA TATTGGAAGT 1980
ATGTCTTCAC CACTCTTTCT CTCTGTACCT TTCTTTAGCC TTTTGAGGTA ACAATATTCA 2040
ATGAGCCAGA TCCTTGGCCG ATAATGGCTA GGCTACTAAC CGATTGAGCT GGAGAACTTA 2100
AGGAAAGCTA CTTTCCCTTT GGAGGCCACT GCTATGCCAT CAATAAAACG AAGAGTTGGA 2160
CCTGTTGATC TAACACCAAT TAATGTGCTG TTAGTTTCTC TGCTGAACCT CTTACGCTAG 2220
AAAAGAGTTC ACTCATGCAT GGACCTTGTT GCAGCTACTT TCCATCCCTG TGCCCAGGGC 2280
TGACATCACT AATCAATCAT ATCCCTCTTT CTGAGAGTAG ACTCAGCCTC ATGCCCCTTT 2340
TAACACACCA CTCTAAGAAG CCAACACCAA TGGAATAGCG TTGTACTCAA GTAGAACACC 2400
CTTTGCCCTC CCAACTCTGT GACTATTCTG ACCCCCTCCC TGTCATTAAA TCATACTTGT 2460
TTATGTTGAA TTAGCCATTT TTTCCCTCCA TCTTAAAGCT GGTGAGGTGG GACTCACTGA 2520
ATCCAATGCT TCTTTGAGCT TGGACATTCT GGGTATCTAT CATTCTCAAG CTGACCTTAT 2580
GTATTTTTAT TGTGATAAAG ATACCAAAAC TAAAAATTGA GACACAATGT TATGCCTCCA 2640
GATATGCTAC CTTGTTTTAT CAGTTCTTCA AAGTCCAGAA TTAAAGAATC TCTCTGTGAA 2700
TTGTCATGTC 2710
|
