| Tag | Content |
|---|
EnhancerAtlas ID | HS158-38564 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr3:47000660-47002700 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr3:47002493-47002504 | GGAGGGTGTGG | - | 6.32 | | RREB1 | MA0073.1 | chr3:47002555-47002575 | TGTGTGGTGGTGTTGTGAGG | - | 6.32 | | Sox6 | MA0515.1 | chr3:47001954-47001964 | AAAACAATGG | - | 6.02 |
|
| | Number of super-enhancer constituents: 36 | ID | Coordinate | Tissue/cell |
| SE_00943 | chr3:47000636-47003247 | Adrenal_Gland | | SE_02008 | chr3:47000692-47002741 | Aorta | | SE_11155 | chr3:46999721-47003820 | CD20 | | SE_14564 | chr3:47000278-47001837 | CD4_Memory_Primary_7pool | | SE_16650 | chr3:46999983-47001584 | CD4_Naive_Primary_8pool | | SE_18708 | chr3:46999601-47003619 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_20061 | chr3:46999416-47002518 | CD56 | | SE_22640 | chr3:46999598-47002488 | CD8_primiary | | SE_23114 | chr3:47000575-47002747 | Colon_Crypt_1 | | SE_23749 | chr3:47000733-47001255 | Colon_Crypt_2 | | SE_23749 | chr3:47001324-47001875 | Colon_Crypt_2 | | SE_23749 | chr3:47002233-47002725 | Colon_Crypt_2 | | SE_26114 | chr3:46999989-47002735 | Duodenum_Smooth_Muscle | | SE_28630 | chr3:46998170-47003223 | Fetal_Intestine_Large | | SE_30558 | chr3:47000885-47002668 | Fetal_Muscle | | SE_31407 | chr3:47000683-47003179 | Gastric | | SE_32585 | chr3:47000613-47001820 | GM12878 | | SE_38780 | chr3:47000232-47003616 | HUVEC | | SE_40617 | chr3:46999813-47003535 | Left_Ventricle | | SE_41619 | chr3:47000640-47002043 | LNCaP | | SE_41619 | chr3:47002075-47002794 | LNCaP | | SE_42118 | chr3:46999822-47003340 | Lung | | SE_47478 | chr3:47000658-47001925 | Pancreas | | SE_47478 | chr3:47001962-47002754 | Pancreas | | SE_48306 | chr3:46999915-47003370 | Psoas_Muscle | | SE_48684 | chr3:47000717-47002767 | Right_Atrium | | SE_49453 | chr3:47000756-47002110 | Right_Ventricle | | SE_49453 | chr3:47002144-47002748 | Right_Ventricle | | SE_50160 | chr3:46999961-47003286 | Sigmoid_Colon | | SE_52388 | chr3:46999875-47002632 | Small_Intestine | | SE_53507 | chr3:47000017-47003202 | Spleen | | SE_58746 | chr3:46966845-47032612 | Ly1 | | SE_59747 | chr3:46966600-47033537 | Ly4 | | SE_60850 | chr3:46965041-47030117 | DHL6 | | SE_62445 | chr3:46966331-47033109 | Tonsil | | SE_64772 | chr3:47001706-47002732 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr3 | 47001323 | 47001648 | | chr3 | 47001666 | 47002342 | | chr3 | 47000781 | 47001063 | | chr3 | 47000667 | 47001400 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I046952 | chr3 | 46993692 | 47003318 |
|
Enhancer Sequence | GGTCTTATCC CCACCTACAC ACACTTCCTT TAGCTACAAA GCGTTTTTAA AAATCCACAT 60
GCTCAGCATA TGGAAAGGTT GAGAAAGCAG AACCACATGA GGAGTCAATA CCCAGCACTA 120
ACAACTGTGT ACTGTGGTAC TCTGGGCCAG TTTAGCTTCT CAGAGCTGCA GTTTCTTCAA 180
CTGCTAGATG GCATGACTTA AGGGTACGCA TGTGAGTGAC AGCCCTACAC TGTGGCTGGC 240
ACAGAGTACG TCCTCAGTCA GTAGGCGCCA ACCACAGTGA TGATGATGGT GGAGCCTGAG 300
ACTCTCACCT GTGTCTTCGG GGTGAGGCCC TCTCATCCCG TGACAAAGGG GTCACATAAC 360
AGATCCCCAC ATTCATGCCT TGTTCCTTCC CTCAGTTCAC CCAGAGCAGC CATCAGTGTC 420
ACCCGGAGGA AGCCCCAGCC CTTGCCCTCG AGCTACCACA GTTGAGAAGA GCAGACCCTA 480
CACGTGTGCA GAGAATATGA ATCCAAGTCA GAAAACGCTA GCCAGTGTGG GGGGACAGGG 540
AGGTGGCAAG GAAGAAGGGC CTTCCACAGA TCATCTTCCC AAATTCAGAC CACCTCCATG 600
CCTGCCTGTT CTGCTCCTGC CCCTCCTCTG CCTAAAATCC CTCCACCTCT TTCACACCTG 660
GAAACAGCTA TCACTCTCCA TGCCATCCAC TCAATCCCTC AAGTGTTTTC TCAGCACCTC 720
TACCAGCTCA GGCTCTGTCT TGTGAGTTAT GCAGCCTGGG ACAAAGCCCA AATGGGGACA 780
CTACTCATAA GCCAACCAAT GAGATAAAGC AGGGTATGTA TATCGATACT GGGTTGAGCG 840
CTCTCCTCCA CGCGACATGC ATGCAAGTGT TGTCCCCCAT CCCCTGTCCA TGCCCTCCCT 900
CCAAGACACT GACAGCTCTC CTCTGCCCCT CCTCCGTGGA TGGCAGTATA CAGTATTATA 960
CCTGGGGGTA CACAGATCAG CCTTCCCACA GGGCCCCAGC CTGACCGTGC TTGAGGCAAG 1020
GGCCAGCCTC ACTGACCCCA TTTCCCACCC AGGCTCTGTG CACAGAGAGG CCTCAACAAT 1080
AACACTTGTA ACAGCCAGAT GTGGAAACTG ACTCCTCACC CCAGACACAG CCCAGCATTC 1140
ACTCTCACTT CCTACATAGA TGGAAGCTGC CTGAGTCATG GACTCCTGGG CCCAGGACAG 1200
GAAAGTCCTG CTTTAACCAG ATGATGTCAA ACACAGGTGC TTTTTCTTCA GGATTCAAAT 1260
TACCCTGCAA GAAATCTAGT GGTGCCCTGC CCTGAAAACA ATGGGAGGGG GGCTGTCCTT 1320
GAAAGGACAA ATGTTTTCTG CTCCAGCCAC TCACATTTTC TCTAGACAGA GCAGCTCTTT 1380
AGAGCCCTGA ATCAAAACAG CCCAGGAGTG TGGATGTTAC TGCCACAGGG CACCGTTGCC 1440
GAAGCAACTG TTTTTCCTCT TGGAATTCTT TCAAGGATAC AAGCTGTTGC TTCCCTCCAA 1500
AACAAAACCA GGGAGAAGCC AGGGCCCCAG AATTTAAGGG AAAGCTCCGA AGGAAGGAAG 1560
AGGGCCAGGC ATGACTGAGC CTTATCAAGC TCGCTATGGG GTCTCCCAGA TCTCCGAACA 1620
ACTGGCTTAG AAACAGCAAG TCCGTCTCAG CTGCTGAAGG TGTATGTGTA GGGAAAGGCA 1680
AATTGTGGGT ATGGAGGTAT AAAGGTGGTG CTGCTTATGT GTGTTTTGAG GTGTGTATGA 1740
GATATGTATT GGTGTAAAGG GGTTGGGGTT TGTAGGTGTG GGTTGGGGGC ATGTGGAGGG 1800
GTGCTGTGGA GTGTTGGAGG TGTGCAGGGA ATGGGAGGGT GTGGGGAGAA GGGAGGTACT 1860
ATTGTGGGGG GAAGTGTGTG GGGTAGGGCC TGGGGTGTGT GGTGGTGTTG TGAGGTTAAG 1920
GGAGTGTAAG GAGGTGGGAT GCACTGTAGG CAGGGGGCTG GGTGTGGAGA GTACATGCTG 1980
TATGTGCATG TGTATATGCG CTGGAGGTGG GTTGGAGGTA TGTGGGATAG GTTACAGAAA 2040
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