| Tag | Content |
|---|
EnhancerAtlas ID | HS179-12066 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr14:65186600-65189160 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxq1 | MA0040.1 | chr14:65186790-65186801 | AATAAACAATA | - | 6.62 | | RREB1 | MA0073.1 | chr14:65188779-65188799 | TCTTGGGGATTGTTTGGGGG | - | 6.44 | | SRF | MA0083.3 | chr14:65187797-65187813 | TTGCCATATAAGGTGA | + | 6.43 |
|
| | Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
| SE_01667 | chr14:65180847-65190201 | Aorta | | SE_03251 | chr14:65186793-65188858 | Brain_Angular_Gyrus | | SE_03953 | chr14:65180662-65189028 | Brain_Anterior_Caudate | | SE_04856 | chr14:65180505-65197762 | Brain_Cingulate_Gyrus | | SE_05821 | chr14:65180438-65199821 | Brain_Hippocampus_Middle | | SE_06781 | chr14:65180403-65192060 | Brain_Hippocampus_Middle_150 | | SE_07938 | chr14:65180667-65190097 | Brain_Inferior_Temporal_Lobe | | SE_08852 | chr14:65187988-65188330 | Brain_Mid_Frontal_Lobe | | SE_19856 | chr14:65187027-65188984 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20478 | chr14:65185982-65194236 | CD56 | | SE_22874 | chr14:65186008-65194196 | CD8_primiary | | SE_23289 | chr14:65182158-65189042 | Colon_Crypt_1 | | SE_24426 | chr14:65186024-65188737 | Colon_Crypt_2 | | SE_26750 | chr14:65181719-65194103 | Esophagus | | SE_27717 | chr14:65181723-65189060 | Fetal_Intestine | | SE_28783 | chr14:65185739-65188904 | Fetal_Intestine_Large | | SE_32308 | chr14:65185993-65188715 | Gastric | | SE_36148 | chr14:65181584-65194566 | HMEC | | SE_47632 | chr14:65186035-65189003 | Pancreas | | SE_49272 | chr14:65187548-65189045 | Right_Atrium | | SE_50477 | chr14:65180818-65190196 | Sigmoid_Colon | | SE_54434 | chr14:65186992-65191038 | Spleen | | SE_57093 | chr14:65186048-65187048 | VACO_400 | | SE_57093 | chr14:65187178-65188964 | VACO_400 | | SE_57603 | chr14:65186014-65188960 | VACO_503 | | SE_64475 | chr14:65185799-65194369 | NHEK | | SE_65298 | chr14:65181865-65199543 | 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 |
| GH14I064714 | chr14 | 65180858 | 65194899 |
|
Enhancer Sequence | TTTGACCTCA AGATGAGAGA GGTGGGGCCT CTGGGAACTT TGGATCTGTC TGTGATTTCC 60
AGGGGGTAAT TTCTAGTAAC ACCTTTTAGG GCTTTCTTTG GCTCTTCCGG TTTTGGGGCA 120
CATTGCATAG TGACAAGTTG TGCTGGCAGC CAAGTTACCT CTACACTGGC TGTGAACAAG 180
AGCAATTTAT AATAAACAAT ACTTGCCCCC ATTTGGCTTT AGCATATGTT TACATGAAAC 240
TTCCTGGCAG ATTGCTTTTC CTGGGACATT TGCAGGGAGA CCAGATCATC ACAGCCCCTT 300
TTCTAAACTT GGCTACTTTC CCCTTCCTCC CAGTCTCTTG TGGCTGGTCA CCTAGTATGT 360
AGCCCAGCGG GGCAGCTATG CCGTGCTCTA GCTCCCTGTC TGGGGCCAAG TAGGATGGGA 420
CTACCGGGGT GAATGAGCAG TCATCAATCC TGGCGCTTCT TGGTTGATCG GAAACTTGCT 480
GGCAGTGACT AATGTGGAGA CTCATTAGGC TAGGAGGAAC TGGCTTTGGT CTTGACCTCA 540
CCCACTGTTT ACCTTTCTCT TGACTGTGTG AGTGGTGAGC TCATCCCGGC GCCATCTCAG 600
AGTCCTTCCA GCAGGCATTT ATTGAACACC TAATGTGCCT TGCTCTCTGG GGCTGAAGGG 660
AAGGTATGGG AAAGAAGGCC CAGCCCACTG GGTTTTACTG TATTGTCCAG AAGAGATGCA 720
TGTACATATC AAGCCCCAAG ACCAATGCTT TAAGTGATAG GGTGTTTCGA GTTCAGAGGA 780
GTATATTACT TCCCTATTGC CACTGTAACA AATTCTGCAA TCTTAGTGGC TTAAATCAAC 840
ACACATTTGT TGTCTTAAAG TTCTGGAGGT AAGAAGTCAG ACTGGGTTTG CATGGCTGGG 900
TTCCTTCTGC AGGATCCAGG GCAGAATTTG TTTCCTTGCT CTTCCTAGCT TCCCAGGCTG 960
CCTGTATCCT TGGCTTGTGG CCCCTTCCTC CATCTTCAAA GCCAGCAGTG TAGCATCTTC 1020
CAGTTCCCTT CTCTCTGTCC CTCTGCTTTT ATTGTCAAAC TTCTGTCTGA CTCTGACTCC 1080
TGCCGGATTC CTCTTACGAG GAGCCTTATG ATCACATCAG GCCCACCGGG CTAATCCAGG 1140
ATAATCTTCC ATCTTAAAAT CCTTGATTTG ATCACATCTG CCTTCTATGT GTCCCTTTTG 1200
CCATATAAGG TGACATTCAT AGGTTGAGGG TCAGGCTGTA GATATCCTTG GGTGGGGGCA 1260
TTATTCAGCT TACACTAGTG TGTATGTTGG GAAATGGTTG AGGAGGCCTT TCTCTGAAGG 1320
AGATGATTGC TAAATGTGTA TAGGCAGAGG GTCTGGGGAC ACATTCCAGG TTTGGGAGAC 1380
AACATGGGCA CATGTTGGGT AGGTGGGGAC AGGGGGGTGT AGATGAACAG CCCTCCCTCT 1440
GAGCTAGGTG CCTGGCTTTC CTTTCCTTCC AAGGTCAGGC CGAGGGAACT TTCTGGACTT 1500
CAGTTGCAGG CCCAGGCTTT CTCCTGGAGT CCATGTGGGA GGGCTCCCCT GGCAACACAA 1560
TCCTTTTCCT TCCTGGCAGC TGTGGTCCTG CTGCAAGGGA CCCAGCCAGA CTACATGGGC 1620
CCTGCTGCTC TTAGGTGGTG GGAAAATGCA TTCCTGAGGG AAAATGAATT TGAACCAGCT 1680
GGGCTGGGTT TGGGTGGCCC AGAAACCTTG GTCACACTGT TGGCACAGCC TCTGCAGGCA 1740
GTCACGTTGC TCACATGCAC ACAAAGTCAC TCCCCGGGGA GCCTTCTCTC GCGCTTTATT 1800
ACGGTGCTCA GGGCTGCTGA ATCTCCAGGA GGGATGGGAG GGGTCAGAGT GAGGAAACTG 1860
CTGGGAAAGG GGGCAAGGGT CCCCTAGGAG GGGGTCCTCC CCTCCCCCAG GAGAGCCCCT 1920
AGGGTGCAGG GAGCAGTGGG AACACACAGG CAAGAGCTGG GCCTCTGGGG ACAGTTTGGG 1980
AGCCGGGTGG CCCAGAGTGG TGCCGAGCTG TGGGTAAGAG CACAGCCGAG GGATTTCACC 2040
ATCTTAGTTG AGATCTTAGT TGAGAGAGAT CTCTCTCTGG AAGTTCACAT TGCTCCCACA 2100
CTGTTTTTTC TGGAAAAGTT ATAGCTTTTC TCTATTGCTT CCTTCTGGCA CCCTTTTTGA 2160
AGGGATTCCG AAAGTGCCGT CTTGGGGATT GTTTGGGGGA AGGACAAAAG CCGCTGGGCC 2220
ACCCTGGCTT TGAGAGCCCT TGGAATGTTT AGCAGATGAT GTAGTTGAGG GATGAAGGCC 2280
ACACAGGAGG GCTGCGCCAT CGCCGTTCCT GAGTGAGGAC TTTCTTTCTT CCTTTCTTTT 2340
TTTGTTTTTG AGATGGAGTT TCGCTCTCAT TGCCTAGGCT GGAGTGCAGT GGTGCGATCT 2400
CAGCTCACTG CAACCTCCTG GGTTCAAGCA ATTCTCCTGC CTCAGCCTCG CGAGTAGCTG 2460
GGATTACAGG TGCATGCCAC CACACCCGGC TAATTTTTGT ATTTTTAGTA GAGATGGGGT 2520
TTCCTCATAT TGGTCAGGCT GGTCTCAAAC TCCTCTCAAA 2560
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