| Tag | Content |
|---|
EnhancerAtlas ID | HS048-00991 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:36598670-36600590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:36600498-36600517 | TGGAGACCCCTGGTGGCCA | - | 6.23 | | ZNF263 | MA0528.1 | chr1:36599336-36599357 | CCACCCTCCCACCCCTCCTCT | - | 6.73 | | ZNF263 | MA0528.1 | chr1:36599634-36599655 | CCTCCCTCCCCCCACTCCCCC | - | 7.33 |
|
| | Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
| SE_01115 | chr1:36599291-36600068 | Adrenal_Gland | | SE_01115 | chr1:36600144-36601228 | Adrenal_Gland | | SE_01636 | chr1:36599006-36604267 | Aorta | | SE_04066 | chr1:36599670-36600906 | Brain_Anterior_Caudate | | SE_05887 | chr1:36598900-36604286 | Brain_Hippocampus_Middle | | SE_07920 | chr1:36599445-36602021 | Brain_Inferior_Temporal_Lobe | | SE_09456 | chr1:36600295-36601519 | CD14 | | SE_18752 | chr1:36600310-36602920 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_25992 | chr1:36600333-36603920 | Duodenum_Smooth_Muscle | | SE_26652 | chr1:36599084-36603413 | Esophagus | | SE_29723 | chr1:36600238-36601746 | Fetal_Muscle | | SE_31707 | chr1:36599253-36599828 | Gastric | | SE_35879 | chr1:36599757-36603157 | HMEC | | SE_37181 | chr1:36599594-36603933 | HSMMtube | | SE_38303 | chr1:36600107-36603567 | HUVEC | | SE_40420 | chr1:36600308-36601944 | K562 | | SE_42156 | chr1:36599361-36603351 | Lung | | SE_44877 | chr1:36599046-36599959 | NHLF | | SE_44877 | chr1:36600155-36603647 | NHLF | | SE_45971 | chr1:36598637-36604352 | Osteoblasts | | SE_48599 | chr1:36599209-36603737 | Right_Atrium | | SE_53482 | chr1:36600002-36602420 | Spleen | | SE_54589 | chr1:36598907-36603542 | Stomach_Smooth_Muscle | | SE_56203 | chr1:36599115-36603890 | u87 | | SE_64339 | chr1:36598887-36603253 | NHEK | | SE_65351 | chr1:36598932-36601064 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 36598993 | 36599761 | | chr1 | 36598923 | 36599578 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I036133 | chr1 | 36598942 | 36603774 |
|
Enhancer Sequence | GTCCCAACTA CTCAGGAGGC TGACACAGAA GAATCGCTTG AACCCGGGAG GCGGAGTGTG 60
CAGTGAGCCG AGATCGTGCC ACTGCACTCC AGCCTGGGCA ACAGAGCAAG ACTCCATCTC 120
AAAAAACAAA ACAAAACACA AAAATTAGCT TGGCGTGGTG GCATACGCCT GTAGTTCCAC 180
CTACTTAGGA AGCTGAGGCA GGAGAATCGC TTGAACCTGG GAGGCGGAGG TTGCAGTGAG 240
CCGAGATTGC GGCACCACAG CACTTCAGCA GCATGGGTGA CAGAGCGAGA CTCTGTCTCA 300
AAAAAAAAAA AAAAAAAAGA ATTCACACAC AGACACAGTC CCTAAGGAAC ATCAGGAAAC 360
AGGCAGACAC TGAAACACAA AAACATACAT ACATAATGTG TAATGTACTG GATAAGAGCT 420
TTGTGTTCAA GTCCTGACTA TCTGGGTTCA AGTGCTGAAT CCACGGTGTT ACTAGCTGTG 480
CTCCTTAGTC TCCTCATCTG CAGATAGTAG TAGGGCTGTG GTGAAGGCTA AATGAGAAAT 540
ACATGTGAAG TACTGGCATA TCACATGACT AGCGCTGGCA CATGGCCACT CTGCAATAAA 600
GATTAGCTAT TGCTATGACT AACATTCATC CACATTCACT GGCAAATGTC CTCCTGCCCA 660
TGCGCACCAC CCTCCCACCC CTCCTCTAGC CTAGCTCAGT CATAGATGCC CTCATGGTTG 720
ACAGTCCAGG CTCCCAGAGC CAAGAGGAAA GAGCAACTGC TTCTCTGCAT CCCCTGGGCT 780
GTACCTGAGC CAGCCCATGT GAGCTCCTCA CCAGCTCTGG GTTCCATCAG AGATGGCTTC 840
CTGGAGGAGG CCTGGACCCA AGGTGGGTGA GGGAGCCAGG GCAAAGCAGG AGAGTGCTAC 900
TCTGTGTCCT GGCTACCTCC ATTGTTCTTT ACAACACCCT CTCCCCCAAC CTCTGCTGCA 960
GCGGCCTCCC TCCCCCCACT CCCCCTTCCC ACAGTAGAAA TTTTCCTCTC TCCCCCTGCC 1020
AGAGTGTAAA TTGCCCCCAG GAATGCAGTG AGTCCCACCG CTCCCCTGGC AGTGGCCGGC 1080
GGCTGTCCTG GGGTCAGGCC TGGCCCTACA TCAAAGGCTG GGGATCAGTA ACAGCAGCTC 1140
CTTGCCTGCC ACCAGCCTCC CCTCCTCTCT CCTACCCTCC CACCGGCCCT TTGGCTTCCA 1200
AAACACAGCA CATGGTAGCA CTTAAGCTCT GGGAGGGCAT TTTTCCTGCA CCCCCACCAC 1260
CTACTAGCCA CAATGAACTA CTTGTTAGGA GACTATTTTA ATTTTACTGA ATGCAATTTC 1320
TGCTCCTGAG GCTTCTGTTG CCACCCGCTT CTTGGCCTTG GATGCCCAGT ACAAATGTAG 1380
GGGAGGCCAA CCCCCTAGGA GAAGGTGAAA CCTGAATATG GAAATTTCAC TGGTGTTGGA 1440
GGTCTGGGGC AGAAAGGGAC AGTGTTACAT CAGGGGAATG GGGCTGGTGC TCTGGCCTCC 1500
ACTCAGGAAG TAAGGGGGGT TGATTAGGGG AGGGCTCAGA GGTAGCTTGT ACACAACTCA 1560
GGAGGCCAGC ATGGGAGTTT GAAGTATGTA TGCGGCCAGA CATCCTTGGC CAACGCTCTC 1620
TTCTAATGTT CTGGCTCCAG CAGGCAGGCG CTTAGCCTGG CAGCTATATG TAAGCTTTGC 1680
TTTCAGGTCC TGTAGGGGTG GCTGGAGGAG GGGGAGCACT CTCAGCCTCC GGTCAGCCTC 1740
TAAGATTTGC TCCATCAGGT GCATCTTCTA GCAAATTCTG AAAACCAGGG GTCCGGTGGT 1800
CACTCTCTGG GACAGTACAG TGGTGATTTG GAGACCCCTG GTGGCCAAAG GCTGAAGACC 1860
GAGACCTTTC CTTAGAGCTC CACCCAGCCA GCCCCAGGCC CAAAGGCCAC CAGCATCAAC 1920
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