| Tag | Content |
|---|
EnhancerAtlas ID | HS180-03147 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:154399230-154401450 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF7L2 | MA0523.1 | chr1:154400148-154400162 | CCCCTTTGATGTCT | - | 6.14 | | ZNF263 | MA0528.1 | chr1:154401281-154401302 | TGAGGAGGAGAGCGAGGGGAG | + | 6.42 |
|
| | Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
| SE_00437 | chr1:154399481-154401751 | Adipose_Nuclei | | SE_01040 | chr1:154399528-154400582 | Adrenal_Gland | | SE_01040 | chr1:154400681-154401626 | Adrenal_Gland | | SE_06653 | chr1:154399347-154403450 | Brain_Hippocampus_Middle | | SE_09189 | chr1:154398672-154408855 | CD14 | | SE_16173 | chr1:154399945-154400671 | CD4_Naive_Primary_7pool | | SE_18405 | chr1:154399517-154407766 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19165 | chr1:154401205-154402489 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_24531 | chr1:154399580-154400359 | Colon_Crypt_2 | | SE_26130 | chr1:154399302-154401704 | Duodenum_Smooth_Muscle | | SE_26877 | chr1:154399516-154400662 | Esophagus | | SE_26877 | chr1:154400694-154402391 | Esophagus | | SE_32086 | chr1:154399571-154400607 | Gastric | | SE_32086 | chr1:154400656-154401897 | Gastric | | SE_41139 | chr1:154399325-154402156 | Left_Ventricle | | SE_41647 | chr1:154399531-154400535 | LNCaP | | SE_41647 | chr1:154400745-154403911 | LNCaP | | SE_42431 | chr1:154399355-154400656 | Lung | | SE_42431 | chr1:154400696-154402137 | Lung | | SE_47983 | chr1:154399591-154400258 | Pancreas | | SE_47983 | chr1:154400922-154401243 | Pancreas | | SE_48261 | chr1:154399318-154401864 | Psoas_Muscle | | SE_48934 | chr1:154399344-154402194 | Right_Atrium | | SE_50453 | chr1:154399516-154401315 | Sigmoid_Colon | | SE_51380 | chr1:154399138-154401914 | Skeletal_Muscle | | SE_52880 | chr1:154399518-154401631 | Small_Intestine | | SE_54618 | chr1:154399097-154409137 | Stomach_Smooth_Muscle | | SE_62668 | chr1:154357227-154415486 | Tonsil | | SE_65390 | chr1:154399323-154400849 | Pancreatic_islets | | SE_65390 | chr1:154400868-154402476 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 154399696 | 154400530 | | chr1 | 154399716 | 154400696 | | chr1 | 154400830 | 154400990 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I154427 | chr1 | 154399576 | 154401508 |
|
Enhancer Sequence | TAATACATTA AAAACAATGT TCGCAATGCT AAAAATATAT TGTTGAAGAT TCTGTGTGAA 60
AGCTATACTG TAGTTGTGGC TTTTTATAAC CCTTTCAAGC CCTCTGGGCA GTAGCAGTCC 120
ACCCCTTATT GCCCTCAGTG GACTTCACCT TCTAGGGACT CAGAATTTTT TTTTTTTTTT 180
TGAGACGGAG CTTCGCTCTT TTTGCCCAGG CTGGAGTGCA GTGGCGTGAT CTCGGCTCAC 240
TGCAAGCTCC GCCTCCCTGG TTCAAGCAAT TCTCCTGCCT CAGCCTCCCA AGTAGCTGGG 300
ATTACAGGAG CCTGCCACCA CGCCCAGCAA ATTTTTTGTA TTTTTAGTAG AGACAGGGTT 360
TCACCATGTT GGCCAGGATG GTCTCGATCT CTTGACTTGT GATCCGTCTC GCCTCGGCCT 420
CCCAAAGTGC TGGGATTACA GGTGTGAGGC CCAGCTGGGA CTCAGATTTT GCTGAGGACC 480
AGGACAGTAC TGTGTGCTGT GTCCTGGCCT TGCAGCAGTG AATGTGTCTC CCGTTTCTCA 540
AGGGCAGGTC TCTGGGATGC CTGACTGTGT CTTCCTTGCC AGTGCCTGGC TGCTGCAGCC 600
TCCTCAAATG TTTATCAAAC ACAGGACTTG CCCACCGTGG GAGAAAGTAA GGCCATAGGT 660
GTCTCAGGAA CCTGCCCAAA CTCGCCTGGC TGCACGGTGA CAATTCAACC AGCTTTCTTA 720
CCCAAGGTCT GTTGGTGACC AGAGAAAACC TTAGATGACC GGCTGCCATG ATGGCCTTAT 780
ATCTGTCCCT TTTCTGCCAG CCTTGAGGTA GAGGGTGCCA GGGAGGAGGA CTCTGGCTCT 840
AGGTGTTAAA GTGAGAGGGA AGTGTGAAGG GTATCTGTAT AGCTAGACAG GGCTCAATGC 900
CAGGCAGAGC TGTCTCCGCC CCTTTGATGT CTATGTCTCT GTCCCTGGAC TGTGGCCAGT 960
AGCCAGTGTG GACTCCAACC TCACCAGCTT TAGGGGTGTT ATCTGCCTGG GAGTCACTGA 1020
TCCTTACTCC CTCCTCTGAC AGCCACCTTG GATGGGGTGA AAGGAAGGAC AGCCTGCCAA 1080
GTATGAGATA AAAACGCCTC ATAAACAAGA AGGGATTTGC AGGCCAGGCA GAGAGCCTTG 1140
TGCTGCTTCT GAGTCCCAGG AGCATGGGCG AGGAGGTGAG GTCAGGCACT CAGCAGCTGC 1200
TGGTCCTCTC TGAAATCTTT GGCCAGATTT ATTGCTACTG CTTGCTAATA AATGGTTATG 1260
CATTTGGTTC AAAGGACCAA GTGTGCTTAC ATGAAAACTG GCTGTGTTCC CTGGCCTCTG 1320
TTTCCTTAGC TGGTTGGACT AATTTGATTG GTTAATAAAT GAGTCCAAGG TGGTTGGGCT 1380
AATTTTTATC TTAGATTCTA TGACTCTATA ACTGCTACTC AAAAAAAGTG TACTTGTTCC 1440
TTTAATCTTT AATCTTATTT TTCTTGAGTA GTAGAATACA CCCAATTTTT TTCAAGGGGT 1500
AGAGAATGCA TTTTTTTTTT AACCTTCCAG TTTGGTCCCT AGAGTAAACA CAGCATTGCT 1560
GTAGTAGATG TAGGGTACTG GAGGGAGCAT GGAACAGGGA ACCAGAAGCC CTGGTTCCTA 1620
CCCCAGCTGG GCATCTGGGC CAGTCTCTTG ATTCCTCTGT GCCTCAGTTA CCAACTATAT 1680
AACGGGCATT CTGCCATGAA TACCCTGCGA TTTGGAAACC TCCTGTGTAC GTGTGCACTT 1740
GGGTGCCTGG CATTCATTCC TAATGGCATC CATTCGTTCA CACATTCATC CAGTACTCAG 1800
CAGACTCCTG CCATGGGCCA GGCAACGTCC CGGGCACTTG GAATATAATG GAGAACAAAG 1860
CAGGGTGCCT ACTTCTGTGG TGCTTGGAGT CTTGAGGGGA AGAGAGACAC GGAATTCGTA 1920
ATTACATGGC AGCGTGTGGG TGACGTATTG CAGAATGAGG GCCTAGTGGA GCTGGGGGAC 1980
CGGAAACGAT GTTTAGGCCG AGACCTGGAA TAGGAGGAGT TGTCGTGGGG ATGATGTAGG 2040
AAGAACGAGT GTGAGGAGGA GAGCGAGGGG AGTTGAGGGG AGGGCTCCAC ACCTTCTAAG 2100
GAGTGGGGAG AGATGAGGCC TCCAAGGACA GAAGGGCCCT GCAGGCCACG CTGAGGAGCT 2160
TGGACTTCAT CTTGTGGATG GTGGCAGGCC CTTGAAGGGT TTTCTAATCC AGGGAGTGGG 2220
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