| Tag | Content |
|---|
EnhancerAtlas ID | HS048-00268 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:10751210-10753930 |
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 | | POU2F2 | MA0507.1 | chr1:10751228-10751241 | TTGATTTGCATAA | + | 6.03 | | 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 | TCTTCCGTAC ACAACCATTT GATTTGCATA ACCCAACCCC CTCTCATAAA AACTGGCTGC 60
TAGTTTAATT AAAAAATGTA AATTTGCTGT CATCTCGGGG CCTGGTGAAT TAGGACGACA 120
TCGGCATTTT TTATTGCTAA AGACGTCCAG ATTGATCCAG CCCTTGGCTG AACTATGGTG 180
GGGGAAAGGG GGTCCACATG GCCCCTGAGG GTCCTGAGGT CCTTCTGTCC CCTCCTGAGA 240
AGGCTTGGCT CTCCCACCAC TGACTTCCTC ATGGCTGAAG GCCTTCAGGA CCTAGATGTG 300
TCCGGGGCCG CGGGGATGTT AACCTACGAT CAGGGAGGCA TGGTGGGTCC ATGATGCCAG 360
CAGCCCTTCG AGGCCTGCGC CCCTGGCCTT GGACTATGTC AGAGAGGCCC TCGGCTGAAG 420
CTGCCCACGC TGCCCCAGAG GAAGGGACCC TCACTTCACC AGCCACGAGC CCCGGCCAGA 480
GACGAGGCCC ATGGCCCCAG CTGTATGCCG TGTGCACTAT GAAGTTGAGG GAGCTGTTCC 540
CAGCTCCTGA AGATGAGCAT GGAGTCAGCC CAGGGACCAG CTCAGAGGGG ATCTCAGCGT 600
CCTCATCTGC TTCCCTTTTT TGGTGAAGTG GGGGGAAGAC TGCTTTTCTT CTGAAGTTCT 660
GAGATTATAA GTGAAACTTC CAAGTTCAAA GAAGAGACTG AGATGGTATC ACCAGATGAC 720
TCCTCCAGGA AACAGTCAGA ACTCTGCCAC CCTGGGCCTC CCCTCTGAGT GGCCAGAGTC 780
CAGGCCTGAG TCCCACTGGG AGTGCTCTAC TCCAGCTACA GGAGGAAGCA GCTGACCTCA 840
GGGTCCCTTC TAGCTTCTAG GAAAAGTTTC CAGAGCCTGT CCCTGGAGTG CTGGGAGAAG 900
TCAGTCTCCC TAAGGCCCAG GAGAGAAGCC ACAAGAGGCT CTGCCACCTG CCTCCTACCA 960
GGGCTGGGAG GCCCTCGCTC CAGTCAGGAC ACCCTAGAGA AGGGCTTTGG AGTACTGTCC 1020
CCACGACAGA CTTGGAGGGA CTGGTTGGTG GATGGCAGGA GGATGGACGC TGGCTCCAGC 1080
TGGCACCCAG GTTAGGAGGA GGCCGACCAG AGGGCCTGCC TTCCAGCTCT GCAATGCCTG 1140
GGTCCTGTGT GCTGGCCCAC AAGCAGAGGC TCTCCTGCCC CAGGTAAGGG GTGGTGCATT 1200
GCCACCAGGC CCATCTCTGA GGTCTGCTTC TTGGCTGGGA TGGGTGGGGG CCCCATTTCC 1260
GAAGAAAGGG GGTGGGGCCT GAGAGGGAGG TGATGAGACA CCGACTGGAG GTGGGGGCAG 1320
GCAGGTTCTC TGTGGGAGTG GAGGGCAGGG AGGGGCAGGG TGGCAGCCTT GGCCTTAGAC 1380
ACCTTTACCA CTTTGCCCAG CAGGGGGTGT CACACCCTTC CCGGGCGCAG AGGTCCCCAG 1440
GCCCTCCACG TCAGACCAGC CAAGATCACA CCTGGTGTCA CACAGTCCTC AAACTCTGCA 1500
AATGACACCT CCCCCCAACA AACACAGGCC CTTCTTCACC GGCCACCGTG CCACCCATCC 1560
TCATCCCCTC AGGGCTGCCT CCGGTCTCTC TGCCCACTGA CCTTTAGAAG GTCAGATATC 1620
AGCTCATGGG TCCCAAGGGC CGATGCTGTG AACTTGGGCC TATTATAAAC AACAACGCTA 1680
ACAGCCACCA GTATCACCTA TCCCATCAAT GAACCAGGAG AGTTCAGAGA TCAGTCTCAA 1740
TGAATGATCG GGCTGCTTGT TTCTTTTAAA ACATTTAAGA AGACAGCTGC TTTTGTCAAC 1800
CTAGCACGTG AGGGTCCTGG TCAAAATTTG GTTTCAATAG CCAGGGCCCA TGGGAAGCCC 1860
GCAAGAGCTG AAGGCAAAAA CACTGGAAAG AATTAGATTA AACCCAAGAA AACACCAAAA 1920
TATCAGGATA AACTGCCCCA GGTGAGCACC AGGCCTCCTG GAGCCCCCGG CCTTGTCCCA 1980
CAGGAGGCCC CCAAACCCAG ATGCCTACGT TGAGTAGTCT GTCTGGTCCA TCACCACCCC 2040
TAGGGTGGGG GCTAAAGAGG CAGGTGGGAG ACAGTCCGGG GCCCCTCACT TTGAACTGAT 2100
AACAGCCACC TCATCCCACA GATTCTCAGG TGAAAAATAC TCATTAGCCA TAATAAGCAG 2160
CTTGATCATC CGACACAGCC TTGTCCCAAA TAAATTAAAT TCCTTTACCT TGAGACAGTC 2220
GCCCCGAAAC CAGACTAACC ACCTTTCCCA ACAGGACGCT GCTTTCAAAA ACTAAACCAC 2280
CCCCCACTAA AAAAATAAAA ACACACACCC CAGAGCCAGA CACACAAAGA TCTTTGCAGA 2340
GAACAAAAAA AAAAAAAAAA AAAAAAAAAA GGCACACACA CAGAAAAAAA ACACGAAGCC 2400
ATACAAAAAA CACGGAGAAC AAAAACCCCA CAAAAACCCC CTAAATCCTC TCTCTGGGTG 2460
CCCCCCAGCT CCTGCTCCTC TCGGTTCTTT CATAATGACA AGCATCACAT TAGTCACAGC 2520
CTCTAAGCAA GTGGCAAATA ACAACAACAA CAGCCTCAGA AGTCGCCGAT CCCGAGGCCG 2580
GGACGCCGGG AGGCAGCCGC CCGACCCTCC CGGCCCCCAC CCGGCCCCGC CGCCACCTCA 2640
TTGGGCTAAA AATAAGAACT TCCGTAAAAG AAGCGAAAGA AAAGTGAAAG AGCCGCCCCT 2700
GCGTTCCCAC CGGCCGGTAC 2720
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