| Tag | Content |
|---|
EnhancerAtlas ID | HS024-00162 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr1:10741280-10744490 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ALX3 | MA0634.1 | chr1:10741659-10741669 | TTTAATTAGA | - | 6.02 | | TCF7L2 | MA0523.1 | chr1:10741389-10741403 | AGAGATCAAAGGGC | + | 6.25 | | ZNF263 | MA0528.1 | chr1:10741292-10741313 | CCCTCATCCCCATCCTCACCC | - | 6.28 | | Zfx | MA0146.2 | chr1:10742953-10742967 | TGGGCCGGGGCCTG | + | 6 |
|
| | Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
| SE_23439 | chr1:10741265-10742010 | Colon_Crypt_1 | | SE_23439 | chr1:10742041-10743529 | Colon_Crypt_1 | | SE_24212 | chr1:10741286-10741703 | Colon_Crypt_2 | | SE_25175 | chr1:10741188-10742076 | Colon_Crypt_3 | | SE_25175 | chr1:10742685-10743189 | Colon_Crypt_3 | | SE_26713 | chr1:10739834-10743868 | Esophagus | | SE_26713 | chr1:10743888-10748903 | Esophagus | | SE_28494 | chr1:10741176-10743659 | Fetal_Intestine | | SE_30102 | chr1:10740351-10744027 | Fetal_Muscle | | SE_31374 | chr1:10732699-10751186 | Gastric | | SE_33519 | chr1:10741115-10749401 | H2171 | | SE_37889 | chr1:10737466-10743900 | HSMMtube | | SE_40607 | chr1:10741152-10758351 | Left_Ventricle | | SE_41555 | chr1:10741274-10741996 | LNCaP | | SE_41555 | chr1:10742068-10744836 | LNCaP | | SE_42099 | chr1:10732695-10754653 | Lung | | SE_48550 | chr1:10741161-10749149 | Psoas_Muscle | | SE_48591 | chr1:10741162-10751093 | Right_Atrium | | SE_54510 | chr1:10711383-10754578 | Stomach_Smooth_Muscle | | 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 | 10742885 | 10743862 | | chr1 | 10741472 | 10741585 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I010662 | chr1 | 10722544 | 10750567 |
|
Enhancer Sequence | TTTTATCCAT TACCCTCATC CCCATCCTCA CCCTGACCTC CACGCCTGGC CCAGGTGGGT 60
CGGGATGGTG GAAGGGTGGA CAGAAGAGCA TGTACGGGGT CAGTCACTCA GAGATCAAAG 120
GGCACAGCCC AGACCCTACT CCACCTGCCA GCCAGCCCAT GTGAGGCAGC GCCCGCCTCT 180
CCCTGCCAGG CCCTCAGCAC GCTGCCCCCT CAGCGGCAGA AACTGCTCCT TCACCTCAGA 240
GCCCGGCCAC CCCTCCTCCT ACACAGCCTT CATGGGTCCC AGCTGACATT TCACTTTCTC 300
TGGGCAGCCT CCCGGGACTG TCCTCTCCCT CTGTCCTCAC TGCACCCTGT CCTAGTCTTA 360
GCACTTTCAT AGTAACTTGT TTAATTAGAC CTCTGCCTCA CCAGACTGCA AGATCCCTGG 420
GACGAGACCA CTGTTTCAGC GCAGTGTCTG GCCCAACAAA TATTGACTGA GTGAATGCAG 480
AAAACCCAGT GCTTCTGGAG CTCGTTAGGG TGGCGCTGGG CCCCAGGGAC GTGGCCTGGC 540
TTCTGGACTG ACCCCCTCGG GGCTCCAGGA ACCTTTCCTG GAGGGGTGGG GTGGGGACTC 600
CCTGGGTGGG ACTGAGCTGA AGCCCCTTCT CTTGGGTCTC TGGCCCTCTT GAGCCCCAGG 660
CTCACCTCCA AACGCCCTTC ACAGGGCTCT ACCCAGAGAA CAAAAGAGGC CCCAGTTGTT 720
CGAACATTTC TCGGCGAGAG GAACAACTGT TGCTGGCCAG TCCCTTTCTG AATAAATCCT 780
GCAACTGTTT GCAGTGAAGT GCGACTCTCT CCCTCCACCT CCTGTCCCTG TCCCAAAAGG 840
AGAAAAGGGG ATTGAAAAAA AGATGGGGGA AAATCCCATA CCAAGCCCCA CCATCTCCCT 900
ACATCCACTT TCAAGTTTGT CTGAAAATGT TATAAACACA ACACACAGGG ACAGCCACCT 960
GCTGTCCCAG ACAACTGGGA CAGCCGCAGC TAAGGGTGAG GCTGTGAGAT CAGGACCCAA 1020
AAACAGGAGG TGAGACAGTG AAGGCTGGAG GGAAGTGGGG GGTGCCGGGA CGGGGAGAAG 1080
GGGCAACGGG AAATATCACC GTGAAGTGGG AGAGGCAGAG GGCAGGGTTG TACTCAGCCC 1140
TGCAGAGGCA GAGGGAGGAG TGTCTGTGGA TCAAGGGCCC CGGAAGACTC CTGGGGGCCC 1200
GGCGGAATCC GGGAGGCAGG AGCTTCCAGT GGGGCAGTGG ATACCGAGAG GGGAAGTAGA 1260
GGAGGGAGAG AAGTTGAGTG GGGAAGAGGG AGCGAGGTCT ATTAAAAACC TCTCAGTGCA 1320
TAACACAAAA TGTCAGGGTT TATAGCTTCA TTCTTGGCTT TGCCGGGACT GAGAACCCTG 1380
AACAGAAATG TCACCGCTTG TCATGTTTAA TCACCTGCTG TTTGTTAACA CCTTCCCTGC 1440
AAGGAGCCTG TCTCAATCTG TCCCTGGGCC CCCCAGGGAC CAGGAAATAG AAAACATCTC 1500
CATCTCCTTC TCTGGGCTCT TGGCCCTGCC TAGGGGCTCT TCAGCTCCAT CTGAAGGCCT 1560
CCCGAGGAGC CCCAAAGTGA TCCTTCCTAT CAGGGAGGCC AGGGAAAGGA ACCCCATATG 1620
GCCCTTGGAG GCGTGGTGCC ATCTGTGGCC CTGCGTGGTG CGCTTGGTGT GGCTGGGCCG 1680
GGGCCTGTCA TCCCCCTGCT TCTTGTGCCT GGCTCTCCAG GCCTGCCTGT CCATTCTAGC 1740
TATTCCACTC GGTCCTCTAA CTCTGCGGGT ACGCAAAGAT AAATAAAGGA GAGCCCGCTC 1800
TGATCTCTGC AGTCTGGAAG TCACCAATCT GTCTGCTTAA ACAGCAACGG TCACATAACA 1860
TCTAACAACC AAAGCCACCA TCCTTCCAGT TACAATCGGA TCACACCATC TGGGGTTCTG 1920
GCTTGGCTCT CTGAGCGTGC TTTCCTGGGT TGTTTAGGCT AGGAATTCTC AGCCCTACTG 1980
CCCCACGTTC CTTCCTCTGG GTTAGGAGTA GGTGTGGGGG AAGGGCAGCA CAAATCTTCC 2040
CCACCTCCTA AAGCACAGTG TGGTCTACAC TGGGAAAGAA GCTGGTTCAC TCTCAGATTA 2100
CAACCAAGCA AAGACCTGGG CAAACTCAAT ACAGCCCCCA GCCTAAAACC CCACCTGGGA 2160
CAGCTGCCTG CAAAGCAGTG AGTTTATCAC GTGGAGTTCC CAAGGCAGCC CCATCACCTC 2220
TAGTAGCAAA GAAAGCCAGT GGAGACACCC ACCGCAGAGC TGAACTGAAA ATGGTCTCCC 2280
AGTGAACCGG GGGGCAAGGT CCCCATCTTC CCTTCCAGCA AGTCTCTGCT TACACAGAAA 2340
CATATCCAGC AAACATGCAT CGTGAACCTG TCTCCTAGGA GAATGCCCGT TCGGTTAGAC 2400
ATGCTTCCTG AAGGGCTCTG CGTCCAGTCC TTTCACTTCC ATTTCACCAC AGAGACAAGT 2460
CGGAGTGCGT TCCACCCACC TGCAACCCTC CCCTGCGGAC AGATGGGAGC ACTCGTTTCT 2520
GCAAAGATGG GCACTCCGGG ATGCCTCTAG AAAAGGAGGC TTTCCCCCAG AAGCTCAAAA 2580
TGCATCTGCA TCAACAACTA CATTTTATCT TGCATCCCTG CAGCCCAGGG ATGTGTTTGC 2640
AGACTACAGG TGGGGTACAC ATCGGGGCCA GAGATGTTTG GGGACGTGGG CCAGGCAGCA 2700
CGGTAGATAC CTAGGGCTGG AGGCCTGTGT GTCCTCACTC AGTGCTGCCA TTTGGAACAG 2760
TGCTCAGGGG CGCCCCGCAC CAAGTCCTCT GACATTTAGC ATTTGGGAAC AAACCCAGCA 2820
GTATCTCCGG GCCTCCAGCT TCCCCACTTA GGAAATGGGA CAGCTCCTTG TCTTCCTCCA 2880
AGGGAACTGA TGAGGAGAGA TGATATGTTA GGTGTGGCTC TCTCGGAAGG AAGGCGCTGA 2940
TAAACTTACG GTGGTGGGGG AGTGAGGGGC TTGGGGGTGG GGGTTCCCTT GTCCGCATCC 3000
TCTCCAGAAG CCCCGTCTGG ACTGTGATAT GTTTGGGGGG AGAAGGCTCA GTGTTAAAGG 3060
GGTGGGATCA CAGCTGCAAG CCCTTTTCTA GGCCGGGTCA AGCTTCCAAG CAGTGCTCTG 3120
CCATGCCTTG GAGGGGGCGG GGAGCGGGGG ACACGAGCAT GCCTGCCCCA GCACACGCGC 3180
CTAGTGGAAC GCAGCGGCCT GGAAGCAAGT 3210
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