| Tag | Content |
|---|
EnhancerAtlas ID | HS113-00303 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr1:12496230-12499440 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:12498279-12498294 | GGTGTCAAGAGGTCA | + | 6.52 | | Sox3 | MA0514.1 | chr1:12496562-12496572 | CCTTTGTTTT | + | 6.02 | | Stat6 | MA0520.1 | chr1:12497689-12497704 | TTTTCTCTGGAAATC | - | 6.39 |
|
| | Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
| SE_00009 | chr1:12492605-12496972 | Adipose_Nuclei | | SE_01743 | chr1:12495152-12496825 | Aorta | | SE_01743 | chr1:12496901-12499606 | Aorta | | SE_03005 | chr1:12495997-12496699 | Bladder | | SE_15065 | chr1:12492619-12497585 | CD4_Memory_Primary_7pool | | SE_15065 | chr1:12497697-12500262 | CD4_Memory_Primary_7pool | | SE_20910 | chr1:12492967-12497444 | CD8_Memory_7pool | | SE_26086 | chr1:12495130-12496765 | Duodenum_Smooth_Muscle | | SE_26716 | chr1:12495112-12496779 | Esophagus | | SE_26716 | chr1:12496922-12499544 | Esophagus | | SE_29231 | chr1:12495587-12496554 | Fetal_Intestine_Large | | SE_29871 | chr1:12492943-12496653 | Fetal_Muscle | | SE_33776 | chr1:12492745-12496835 | HCC1954 | | SE_33776 | chr1:12496879-12499544 | HCC1954 | | SE_39882 | chr1:12492813-12499393 | K562 | | SE_41209 | chr1:12495188-12496727 | Left_Ventricle | | SE_41209 | chr1:12496898-12497713 | Left_Ventricle | | SE_41209 | chr1:12497794-12499586 | Left_Ventricle | | SE_42647 | chr1:12495092-12496753 | Lung | | SE_42647 | chr1:12497888-12499604 | Lung | | SE_45864 | chr1:12493103-12496844 | Osteoblasts | | SE_45864 | chr1:12496857-12498598 | Osteoblasts | | SE_49026 | chr1:12495807-12496754 | Right_Atrium | | SE_50544 | chr1:12495565-12496682 | Sigmoid_Colon | | SE_51539 | chr1:12495449-12496864 | Skeletal_Muscle | | SE_52815 | chr1:12495340-12496737 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 12498363 | 12499182 | | chr1 | 12497806 | 12498000 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I012432 | chr1 | 12492844 | 12500570 |
|
Enhancer Sequence | ACACACATGT GGGAAAGTGT TCCAGGTTTG AGTTTGGTGT CTGTGGGGGT TCCTGTAGGG 60
GGATCTCAGG AAGGGGTGGA CTCTTCTACC CAGGACAAGG AAGGTCTGTA CAGGGGAAGG 120
CACGCCGGTG CCCAATCCTG AAGTCCAAGG AGATGCTTGC CATGTGGACA AGAGACAGGT 180
GGGGACAAGA AGAGGCACAC AGGGAGCAGT CCCAGCAGGA GGGAGCCTGG GGTGTGCAGC 240
AGCAGGACTA GGGAGGGGTC AGTGGAGCTT AGCAGGTGGG CCTCTGGAAT GAGGAGCTGG 300
CCTAGTGGGG AAAGACTGGC TCATTGTACA TCCCTTTGTT TTCCCTTGTT TCGCCCCCAC 360
CCACCACGTG AATTTAAAGG GGAAGAGACT TAACTGAATG TTTCACTTTT TGAGCCTAGT 420
ATTGTTATTT GTCATGATTT GACCATAATC TGCATATATA CAATGTTAAC TATTATTTTT 480
TGCAAGTTTT TTTTTGTTTG TTTTTGTTTT TGAGACGGAG GTTTGCTCTT GTTGCCCAGG 540
CTGGAGTGCA ATGGCGTGAT CTCGGCTCAC CGCAACCTCC GCCTCCCAGA TTCAAGCAAT 600
TCTCCTGCCT CTGCCTCCCG AGTAGCTGGG ATTACAGGCA TGCACCGCCA CGCCTGGCTA 660
ATTTTGTATT TTTAGTAGAG ACAGGGTTTC TCCATGTTGG TCAGGCTGGT CTCGAACTCC 720
CGACCTCAGG TGATCCACCC ACCTCAGCCT CCCAAAGTGC TGGGATTACA CGCGTGAGCC 780
ACCGCTCCTG GCCTTTGCAA GTATTTTTAT GTGGGTAAAA CAGTTATACC TTTCACTGAG 840
CGGGCCCAAA CAAACAAAAA CAACAGCCTG TCACACCGTG TGTGTGTGTG TGGCGGCGGG 900
AGGGGGGTAC CCAAAAACCC TGACTCACTT TTTATATAAT TAGAGCTAAA ACCAAACCAA 960
GTCATGGCTT GTTTGCAGTA GGTAGATTGC AGAGTTACCA AACTGTTCTT TCTGACCAGA 1020
GTGACTCAGT CTAGTGCAAA GTCATGAACT GCCTCCAGCA TTTCTCATTA ACCTAATATC 1080
TCCATCTAGA GTAGAAATTC ACCCTCCCTA AAGCCCAGAG GAAACAAACT AAGGGTCCTT 1140
GTGAAAGGAA AAGGCCTTTA GACCCTAAAA CAACTGATTA GAAAGGCAGG ACGAAAGGAG 1200
GGAGGGGGGC ATTCTTTGTG CTTTCCTGTG CAATTTGGAG CTCAACAGAT GAAGTGTTTG 1260
CCATTGATCC CCAAACCACA TTTTGGGAAA CTATCTGACC CCATTTGACT GGCCATTCAA 1320
CTGTTCCACC ATTTTCTTTA CACAAAGCTA AACTAGATTT GAGCTAAATT TGAGAGGGAA 1380
GAGCACATTA CATATGGGAA TGTGGTTCAT GGTTTTCTAA CCCAACCCTC CCCTCCCCCA 1440
TCCATTCCAA TGAGTAGATT TTTCTCTGGA AATCCATCCT TTCTTTTTCC ATTCAAGGCA 1500
ACTAACAGTA TCCAATTTTT GATTCGTAGT TTTAGTTTTC CATGTATAGA CTAAAAGTGG 1560
ATGTTTATCT TGAGACAGGA ATGACTGTTT TTCTGCAATT GTTTAGACTA AGGCTAGGTA 1620
GATTTCCTGT GGACTTCTTG GAACCTTTGA GCCCTGATGT TTTCCCTGCG CTCAAAAATT 1680
ACAGTGCTGG ATGGCATCTT TCCAGCTGTT GGGATGGGAG ACAGGCTGGG CCCTTTGACT 1740
CCTAAAATTG AACTTAGGTT GAGCTGGTTG GCAAATGTGG CAATGAAAGG GTTCCCTGAG 1800
CAAAACCTGG GAAAATATCA GTCTGGATAT ACTCTCCTAG CCCTGGCTTT CTTAGCACAC 1860
CTTGATGTGT GTTCCGTAGC TGTCTTCCCA CCCCCATCCC CTAAAACTTG AGCATCTGTA 1920
GCTCATCACT TATGTCCTGA ACTCAGTAAA CTGAGTCTCT GTTATAGGAC TTAGAGAAAT 1980
TTTCTTATAC TATGGACTGA ATGTGTCCCC CCAGAATTCA TATGTTGAAA TTCTAACCCC 2040
AAAGGTGTTG GTGTCAAGAG GTCATTGGGG GTGATTAGAT CAAGGAATTG GTGCCCTTAT 2100
CAAAGAGACC CCAGAGAGCT AGCCCACCCT TCTACCGTGT GAGGTTACAG TGAAAAGATG 2160
GCCATCTAGG AAGCAGGCCC TCATCAGACA TTGAATCAGA CACCGAATCT GCTGTCACCT 2220
TGATCTTGGA CTTCCCATCC TCCAGAACTG TGAGAAACAA ATTTCTGCTG TTTGTAAGCC 2280
ACTCAGTTAA CGGTATTTTG TTGTAGCAGC ATGAACACAC TGAGACAGCA CATAACACAG 2340
AATGCTGTTT CTTTAAAATT TTCTTGAGTT TTTACCATGT GGTTTACTTG TCTTTTTCAT 2400
TGATCCTTCC CTGTTCAGTG GGGAAACACA GATCAGCACC CAGCCCTTGC CGACCACATG 2460
AAACCTAAGA TCTCACCTCC TCCTCCCTGG CAAAAGAAGA ATTAGATAAT GAGAGGTGTT 2520
CTGGTTTTGA GAGGAAGTTA ACAAGTGTTG GGACGCTTGC ACGTTAGAGC TGGCTGCCTG 2580
TGCTCTGAGT CAGAACTGAA ATTTTGACAT GTAAAGAAGA ACTAATATTT GATCCTCTCC 2640
TGTGTGCCAG GCATAGCGCT AGCCACTTCA TAGCTTTTTG GCTATTCTTC TCCATCTCCT 2700
TTCTGCCAGT TGCTCAAATA CTTTGGAGTC ATCCTTGGCT CCTTTCGGTC ATGCCGCATG 2760
TCCAGTCCCT CAGCAGATCC CGAATCTGAA CATATCCCTC CCGCGCCCAC CTTCTAGTCC 2820
TCGTTCATCT TTGGCCTGGT TTTTATTGTA GTACACTTCT CCTTGCACCC TTGCTTCCTA 2880
CTACTGACAT TGAACCTCAG TACAACAACT AGAGTGATCC TGTCAAAACA TAACAGATTT 2940
GGTCACCCAG CCCCTCCAGA GGCTTCCCGT TTCACTCCAC ATAGAAAATT CCAGCTTGTG 3000
CAACCTCACG AAGCCCACGA GGTCAGCCTC CTGCAGGCCT TTTCTGACCT GGTGCCTCAC 3060
TGTCTCACCA CCCTCCACCC CTCACCAGCT CCTGCCACAC TGTTCTCGCT GCTTCTCAAC 3120
CCTCTGCCTT CAAACGTCCA CTCCAAGGTC TCTGCACTCA GTGTTCTCTT CCTGGAATGT 3180
TCTATGGCCA CATGGTTTTC ATCTACATTT 3210
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