| Tag | Content |
|---|
EnhancerAtlas ID | HS051-00178 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr1:10751440-10753930 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:10753884-10753905 | GAAAGAAAAGTGAAAGAGCCG | - | 6.2 | | ZIC1 | MA0696.1 | chr1:10752605-10752619 | CCCAGCAGGGGGTG | - | 6.06 | | ZIC3 | MA0697.1 | chr1:10752604-10752619 | GCCCAGCAGGGGGTG | - | 6.26 | | ZIC4 | MA0751.1 | chr1:10752604-10752619 | GCCCAGCAGGGGGTG | - | 6.02 | | ZNF263 | MA0528.1 | chr1:10753670-10753691 | CCCCCCAGCTCCTGCTCCTCT | - | 6.25 |
|
| | Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
| SE_23439 | chr1:10751268-10754639 | Colon_Crypt_1 | | SE_24212 | chr1:10751320-10751841 | Colon_Crypt_2 | | SE_24212 | chr1:10751902-10752976 | Colon_Crypt_2 | | SE_24212 | chr1:10753583-10755727 | Colon_Crypt_2 | | SE_25175 | chr1:10751275-10753513 | Colon_Crypt_3 | | SE_25175 | chr1:10753578-10755827 | Colon_Crypt_3 | | SE_26713 | chr1:10751334-10756903 | Esophagus | | SE_28494 | chr1:10751152-10754734 | Fetal_Intestine | | SE_30102 | chr1:10753603-10754685 | Fetal_Muscle | | SE_31374 | chr1:10751200-10758378 | Gastric | | SE_33519 | chr1:10752816-10756047 | H2171 | | SE_40607 | chr1:10741152-10758351 | Left_Ventricle | | SE_41555 | chr1:10751283-10751953 | LNCaP | | SE_41555 | chr1:10751958-10752993 | LNCaP | | SE_42099 | chr1:10732695-10754653 | Lung | | SE_47486 | chr1:10751945-10752438 | Pancreas | | SE_47486 | chr1:10753613-10754480 | Pancreas | | SE_48550 | chr1:10752428-10753543 | Psoas_Muscle | | SE_48550 | chr1:10753580-10754631 | Psoas_Muscle | | SE_48591 | chr1:10751288-10754634 | Right_Atrium | | SE_49447 | chr1:10752003-10753385 | Right_Ventricle | | SE_49447 | chr1:10753560-10754467 | Right_Ventricle | | SE_54510 | chr1:10711383-10754578 | Stomach_Smooth_Muscle | | SE_57180 | chr1:10751888-10752493 | VACO_400 | | SE_57180 | chr1:10753611-10754575 | VACO_400 | | SE_63296 | chr1:10733447-10756197 | NCI-H82 | | SE_65281 | chr1:10740888-10754570 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 10751516 | 10751566 | | chr1 | 10751800 | 10752217 |
|
Enhancer Sequence | CCTCCTGAGA AGGCTTGGCT CTCCCACCAC TGACTTCCTC ATGGCTGAAG GCCTTCAGGA 60
CCTAGATGTG TCCGGGGCCG CGGGGATGTT AACCTACGAT CAGGGAGGCA TGGTGGGTCC 120
ATGATGCCAG CAGCCCTTCG AGGCCTGCGC CCCTGGCCTT GGACTATGTC AGAGAGGCCC 180
TCGGCTGAAG CTGCCCACGC TGCCCCAGAG GAAGGGACCC TCACTTCACC AGCCACGAGC 240
CCCGGCCAGA GACGAGGCCC ATGGCCCCAG CTGTATGCCG TGTGCACTAT GAAGTTGAGG 300
GAGCTGTTCC CAGCTCCTGA AGATGAGCAT GGAGTCAGCC CAGGGACCAG CTCAGAGGGG 360
ATCTCAGCGT CCTCATCTGC TTCCCTTTTT TGGTGAAGTG GGGGGAAGAC TGCTTTTCTT 420
CTGAAGTTCT GAGATTATAA GTGAAACTTC CAAGTTCAAA GAAGAGACTG AGATGGTATC 480
ACCAGATGAC TCCTCCAGGA AACAGTCAGA ACTCTGCCAC CCTGGGCCTC CCCTCTGAGT 540
GGCCAGAGTC CAGGCCTGAG TCCCACTGGG AGTGCTCTAC TCCAGCTACA GGAGGAAGCA 600
GCTGACCTCA GGGTCCCTTC TAGCTTCTAG GAAAAGTTTC CAGAGCCTGT CCCTGGAGTG 660
CTGGGAGAAG TCAGTCTCCC TAAGGCCCAG GAGAGAAGCC ACAAGAGGCT CTGCCACCTG 720
CCTCCTACCA GGGCTGGGAG GCCCTCGCTC CAGTCAGGAC ACCCTAGAGA AGGGCTTTGG 780
AGTACTGTCC CCACGACAGA CTTGGAGGGA CTGGTTGGTG GATGGCAGGA GGATGGACGC 840
TGGCTCCAGC TGGCACCCAG GTTAGGAGGA GGCCGACCAG AGGGCCTGCC TTCCAGCTCT 900
GCAATGCCTG GGTCCTGTGT GCTGGCCCAC AAGCAGAGGC TCTCCTGCCC CAGGTAAGGG 960
GTGGTGCATT GCCACCAGGC CCATCTCTGA GGTCTGCTTC TTGGCTGGGA TGGGTGGGGG 1020
CCCCATTTCC GAAGAAAGGG GGTGGGGCCT GAGAGGGAGG TGATGAGACA CCGACTGGAG 1080
GTGGGGGCAG GCAGGTTCTC TGTGGGAGTG GAGGGCAGGG AGGGGCAGGG TGGCAGCCTT 1140
GGCCTTAGAC ACCTTTACCA CTTTGCCCAG CAGGGGGTGT CACACCCTTC CCGGGCGCAG 1200
AGGTCCCCAG GCCCTCCACG TCAGACCAGC CAAGATCACA CCTGGTGTCA CACAGTCCTC 1260
AAACTCTGCA AATGACACCT CCCCCCAACA AACACAGGCC CTTCTTCACC GGCCACCGTG 1320
CCACCCATCC TCATCCCCTC AGGGCTGCCT CCGGTCTCTC TGCCCACTGA CCTTTAGAAG 1380
GTCAGATATC AGCTCATGGG TCCCAAGGGC CGATGCTGTG AACTTGGGCC TATTATAAAC 1440
AACAACGCTA ACAGCCACCA GTATCACCTA TCCCATCAAT GAACCAGGAG AGTTCAGAGA 1500
TCAGTCTCAA TGAATGATCG GGCTGCTTGT TTCTTTTAAA ACATTTAAGA AGACAGCTGC 1560
TTTTGTCAAC CTAGCACGTG AGGGTCCTGG TCAAAATTTG GTTTCAATAG CCAGGGCCCA 1620
TGGGAAGCCC GCAAGAGCTG AAGGCAAAAA CACTGGAAAG AATTAGATTA AACCCAAGAA 1680
AACACCAAAA TATCAGGATA AACTGCCCCA GGTGAGCACC AGGCCTCCTG GAGCCCCCGG 1740
CCTTGTCCCA CAGGAGGCCC CCAAACCCAG ATGCCTACGT TGAGTAGTCT GTCTGGTCCA 1800
TCACCACCCC TAGGGTGGGG GCTAAAGAGG CAGGTGGGAG ACAGTCCGGG GCCCCTCACT 1860
TTGAACTGAT AACAGCCACC TCATCCCACA GATTCTCAGG TGAAAAATAC TCATTAGCCA 1920
TAATAAGCAG CTTGATCATC CGACACAGCC TTGTCCCAAA TAAATTAAAT TCCTTTACCT 1980
TGAGACAGTC GCCCCGAAAC CAGACTAACC ACCTTTCCCA ACAGGACGCT GCTTTCAAAA 2040
ACTAAACCAC CCCCCACTAA AAAAATAAAA ACACACACCC CAGAGCCAGA CACACAAAGA 2100
TCTTTGCAGA GAACAAAAAA AAAAAAAAAA AAAAAAAAAA GGCACACACA CAGAAAAAAA 2160
ACACGAAGCC ATACAAAAAA CACGGAGAAC AAAAACCCCA CAAAAACCCC CTAAATCCTC 2220
TCTCTGGGTG CCCCCCAGCT CCTGCTCCTC TCGGTTCTTT CATAATGACA AGCATCACAT 2280
TAGTCACAGC CTCTAAGCAA GTGGCAAATA ACAACAACAA CAGCCTCAGA AGTCGCCGAT 2340
CCCGAGGCCG GGACGCCGGG AGGCAGCCGC CCGACCCTCC CGGCCCCCAC CCGGCCCCGC 2400
CGCCACCTCA TTGGGCTAAA AATAAGAACT TCCGTAAAAG AAGCGAAAGA AAAGTGAAAG 2460
AGCCGCCCCT GCGTTCCCAC CGGCCGGTAC 2490
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