| Tag | Content |
|---|
EnhancerAtlas ID | HS134-02446 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:94086140-94088780 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE41 | MA0636.1 | chr1:94086979-94086989 | GTCACGTGAC | + | 6.02 | | BHLHE41 | MA0636.1 | chr1:94086979-94086989 | GTCACGTGAC | - | 6.02 | | HNF1A | MA0046.2 | chr1:94087866-94087881 | AGTTAATGATTAAAA | - | 6.2 | | HNF1A | MA0046.2 | chr1:94087866-94087881 | AGTTAATGATTAAAA | + | 6.73 | | HNF1B | MA0153.2 | chr1:94087867-94087880 | GTTAATGATTAAA | - | 6.07 | | HNF1B | MA0153.2 | chr1:94087867-94087880 | GTTAATGATTAAA | + | 6.48 | | MITF | MA0620.2 | chr1:94086975-94086993 | AAGAGTCACGTGACCAAA | + | 6.86 | | MITF | MA0620.2 | chr1:94086975-94086993 | AAGAGTCACGTGACCAAA | - | 6.86 | | Nr5a2 | MA0505.1 | chr1:94087668-94087683 | GCTGGCCTTGAATTC | - | 7.03 | | Pou2f3 | MA0627.1 | chr1:94087961-94087977 | TCTTATGCAAATCTGA | + | 6.26 | | USF1 | MA0093.2 | chr1:94086979-94086990 | GTCACGTGACC | + | 6.14 | | USF2 | MA0526.2 | chr1:94086977-94086993 | GAGTCACGTGACCAAA | - | 6.44 | | ZNF263 | MA0528.1 | chr1:94086196-94086217 | TCCTCCAGCCCCACCTCCTCC | - | 7.11 |
|
| | Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
| SE_02655 | chr1:94087911-94090618 | Astrocytes | | SE_31653 | chr1:94085873-94086755 | Gastric | | SE_31653 | chr1:94086889-94087481 | Gastric | | SE_31653 | chr1:94087881-94088737 | Gastric | | SE_36105 | chr1:94087927-94090600 | HMEC | | SE_37879 | chr1:94088352-94091766 | HSMMtube | | SE_38536 | chr1:94087600-94095889 | HUVEC | | SE_45907 | chr1:94086553-94090565 | Osteoblasts | | SE_52025 | chr1:94087811-94090608 | Skeletal_Muscle_Myoblast | | SE_63816 | chr1:94086974-94087705 | HSMM | | SE_63816 | chr1:94087811-94091970 | HSMM | | SE_65777 | chr1:94085057-94086790 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr1 | 94087621 | 94088167 | | chr1 | 94088249 | 94088511 | | chr1 | 94086372 | 94086708 | | chr1 | 94087878 | 94088738 |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH01I093620 | chr1 | 94086161 | 94086310 | | GH01I093622 | chr1 | 94086357 | 94086610 | | GH01I093621 | chr1 | 94086943 | 94092719 |
|
Enhancer Sequence | GTTGCAGAAT TGGACTTCAG CCTCAGTCCT GATTGGATGC CCTACAGGAT CCTCACTCCT 60
CCAGCCCCAC CTCCTCCTGC CCTGGCCCTG CAATTCAGCC CTGGGAACAG ATCTTCCACA 120
TGTGTTTAGC ATCCCCAGAG AACCACCTCT CACATGCCGA CTCCTTCATA TTTCCCCGCC 180
CTGTATTACT GGGTTGTCTG ATACCAACCA ATTCTAGAAC TACAACCGTG TCTGGTATAG 240
CTCCTCAGAT GTTGTGACCC CTCTGCCCTC TCTAGACTTT CTCTCTGTGT CCTCCCAGAT 300
ACTGCCTTCT GCCTAGATCT CCTTCTCTCA AGTCCCTAAT GGCAGGAATC TGCCAGAGTT 360
ACAGTGCATT CTTCTAAAGC CACACATCCC TATCTCCACC TAGAAAGGCT GCCAAGTGGC 420
TGAGTGGATG AACCTGCCTG CAAGGGATCA CCCGCCTAGG AAGGCAGGAA CCCAGGGGCG 480
GAGGGCGGGG TCAGTACCAG GTGAGAGGTG GAGTCAGGAG TAACCCCACC CATTCCAGCC 540
TGGAGAGAAA ATGGTCTTAT CAATCGCTTT TCTGTTGTCA AGCAAATTCT AGCCATGCAA 600
ACAAAATATT TCAGTGGGAA AATATCTCTT TTTCATGGTC ATAAGCTGAT CATGGGCATT 660
ACCATCTAAG TGACGTACTG GATAATTCTG TATCCTGCCA AAGTAGCTGT GAGAATCAGT 720
CCAGATGAGG AGTTCTGAAC CTAGGGGTGG ACTGGGGCTT CCATGGGCCA CTAGAAACTG 780
TATACAAATT GTTGTGTTCA TTGAGGAGAG GGGTTATGAC TTTTACCCAA TTTCAAAGAG 840
TCACGTGACC AAAAAATTCC TTCTGATCCA GAAAGACTTT CAGTGGCATG TAGGAAGGGA 900
GGTGAGAATA CCTTGGTGGT CACAGAAGTG AGTACGGACT GATAAAGCAC CCTGGCTGGC 960
CACCTTGCAC ACACCCGGGT TGTAGCAGGG ATGTGGCTGG TAAGAGGAGG GGATAGATAG 1020
CCTTGAGGCA AGTAGTATTG CAGTTTCTTA TGGCCGCTGG AGCAGCTTTA ACCAGCACGG 1080
GAACCCCTTC ACTCAGTGGG TGGATGGACC TTGTTTGCAT GTAATACTTA GGACAGAAAA 1140
TTGGAAGAGC TACAAGTTTG ACTCTCAACA ACCCCTCCTC ACCACAGACT TCAGAGATGC 1200
CTTGAAGAAG CCTGCAGCCG TCACAGATAT CGTTTCACCT CACTCACCCC ATGTGAAAGG 1260
TCCCCAGAAG CCACATTGGT TTTGTTTTTG TTTTTGTTTT TGTTTTGAGA TGGAGTCTCA 1320
CTCTGTCGCC CAGGCTGGAG GGCAGTGGCG CAATCTCAGC TCACTGCAAC CTCCGCCTCC 1380
CGGGTTCAAG TGATTCTCCT GCCTCAGCCT CCCGAGTAGC TGGGACTACA GGCACCCGCC 1440
ACCATGCCTG GCTAATTTTT GTATTTTTAG TAGAGATGGG CTAATTTTTG TATTTTTAGT 1500
AGAGACACAG TTTCATCATA TTGGCCAGGC TGGCCTTGAA TTCCTGACCT TGTGACTCAC 1560
CCTCCTAGGC CTCCCAAAGT GCTGGGATTA CAGGCGTGAG CCACCATGCC AGGCCAGGAG 1620
CCAGCACTTC TACAGAGAAC TTTTACCATG GTGTCCTATT TCATAGTCAC ACTAGGAGAG 1680
GAGTATTATT ATCTCCATTT CACATGTGGG ATCAAACAGC TCTTAAAGTT AATGATTAAA 1740
ACAACAACGA ATCAGAATGG CTGGCTCTAT CTGGTGTGAT GAGGGAAGCA CGGAGAACAC 1800
CTGGTCACCA GAAGTGCTTT ATCTTATGCA AATCTGAAAG GCAGACCTCC CTCCAACAGA 1860
GGGACAGATA CTCTTGGCAA CACAGGCAGC AGATCTCATC TGCAATAGTC CATCAGAGGT 1920
CCTATTCCGC TCACAGCTGA AAGGAAAGTG CAGGGCTGGG AGAGATGGAT GCTGACATCA 1980
GAATCTGAGA AGAACCAGGA GGCAACAAAG GCTTGCTGCA CAAGAAGGGC TAAGGGACCG 2040
CTTTTGTCAC ATGGAAACAC AAACAGTACC CCTTCCTCTA TAGGAAGAGG CCAATTCAGA 2100
GGGTTCTGTG CATGGAAGGA CCTCATTGAC TGCCGGCCAG TTTCTTCACT TCCTAACGTA 2160
GTCAACTGCC AAGCATAATG CTGTCTGCAG GAGTGACATC CAGAAGGTCA ATATTTGCCC 2220
TTCCTGGTGC CAAGGTGGGG ACAATAAATT CCTTTGCCAG TGGCTCAAAG ATTTGGGTAC 2280
GCCTTGCAGT GTATATCCAA ATGGGTGGAA GGGCTGGGTG GAGGAAGGGA GAATTACTAG 2340
GGAGAGCAGC AGAAACCCAT CTGGGTAACT ATCCAGGAAC ACCAGGACTC CCGGTTGGGT 2400
CACTTGTGAT AAGATGTGGG AATCCATCCA AGGACAAGCT ATAGATGGGC TGGGGATCCA 2460
CAGCCCCTCT GGACATCCCC ACCCCCTGCC CATAACTTCT CTGTAACAGT AGCAAATCTG 2520
GCAAACTTGG AGGCAATGGG TATCCAGTAC ATAAACCAGG AGGGAGATAA ACTAGGGAAA 2580
GATGGGAATA GGACTTGAAA AGATTTTCTT TTTTTTCGCA AAACTTAGCA TTCATGTCTC 2640
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