EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS158-17921 
Organism
Homo sapiens 
Tissue/cell
Pancreas 
Coordinate
chr14:91869170-91870800 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs117297873chr1491870330hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr14:91870615-91870636ATCCTCTCCTTCCCCTCCTCC-6.97
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_03973chr14:91868501-91869636Brain_Anterior_Caudate
SE_09196chr14:91868323-91871210CD14
SE_10890chr14:91853239-91874080CD20
SE_11838chr14:91867869-91874199CD3
SE_14423chr14:91867825-91878373CD4_Memory_Primary_7pool
SE_15581chr14:91868198-91873746CD4_Memory_Primary_8pool
SE_16257chr14:91868680-91869818CD4_Naive_Primary_7pool
SE_16329chr14:91867866-91878413CD4_Naive_Primary_8pool
SE_16861chr14:91868494-91870042CD4p_CD225int_CD127p_Tmem
SE_16861chr14:91870119-91871173CD4p_CD225int_CD127p_Tmem
SE_17338chr14:91867815-91886176CD4p_CD25-_CD45RAp_Naive
SE_17763chr14:91852838-91886281CD4p_CD25-_CD45ROp_Memory
SE_18257chr14:91867732-91886272CD4p_CD25-_Il17-_PMAstim_Th
SE_19104chr14:91867817-91874225CD4p_CD25-_Il17p_PMAstim_Th17
SE_19998chr14:91867824-91884134CD56
SE_21071chr14:91867635-91878274CD8_Memory_7pool
SE_21656chr14:91868189-91874026CD8_Naive_7pool
SE_21949chr14:91867747-91878386CD8_Naive_8pool
SE_22293chr14:91852641-91884153CD8_primiary
SE_31363chr14:91868619-91870129Fetal_Thymus
SE_31609chr14:91867949-91871118Gastric
SE_39415chr14:91868917-91870072Jurkat
SE_39415chr14:91870172-91871126Jurkat
SE_41633chr14:91869178-91870093LNCaP
SE_41633chr14:91870127-91870808LNCaP
SE_43558chr14:91868926-91869931MM1S
SE_50173chr14:91867864-91871145Sigmoid_Colon
SE_52486chr14:91867931-91870114Small_Intestine
SE_52486chr14:91870152-91871020Small_Intestine
SE_53934chr14:91868949-91869857Spleen
SE_58376chr14:91781648-91886211Ly1
SE_58849chr14:91813006-91886123Ly3
SE_60717chr14:91860252-91886040DHL6
SE_61123chr14:91814842-91881922HBL1
SE_62324chr14:91813043-91886085Tonsil
SE_66290chr14:91868917-91870072Jurkat
SE_66290chr14:91870172-91871126Jurkat
SE_67160chr14:91868926-91869931MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr149186932291869469
Enhancer Sequence
AAACAATAAA GGAAAAAGAA AAGGGCTGGG AGAAGCTAAG GCACCCGGGC TGTATTTATT 60
CTGCTGTTTC ACTTGAGATA AGGAACCTTC TGGCCTTGTG CCCATGCTAG AGGCCAGAAG 120
TCAGAGAGCC GAGCTCAAGG AACCCAGAAA GCTAAACTTC CTTGAGCTGA TCGTAAACTC 180
TAAATCTCCT CTAAATCTCG CAGTTTCTGG TCACCATGCA ACTGTAGCAT TTCAGGCCCA 240
CCCCCTTTTG CTTGAAGGAG GGCACTCAGG AGGCTCAGAG AAGGAGAGCA GCCCGCCCAG 300
AGAGACGGCG GGACCCCAGC CTTGCTGCCT CTGCACCTGG CGAGGAGAGG CGCATGAAGA 360
AACAGCAAAT TCCTCATTTC AGAGTGAATC CAATGGGTAA GTCCCCACAT CCATCCAAGG 420
GTCCCGATCT CACTGGATGA GATATCCACG TGTGGACTCG ATGACAAAGA CATACGTCTC 480
CAACAACACA CAGGGAATGT ATCCAGGCCA CCATCTGAAG TGCTTCCCGC CATACAAAGC 540
CAAAGAAACC TCAGAAACTT CACATGACAA TGAGGCCCTT TCCAGACAAG GCGCCGGACT 600
GAAGGTGTCC AGGGCAGGGA ATGGGGATGG GATGCCAGGC ACAACCCCAG AGCACAGACA 660
GGCCAGCCAC TGCTGCACAG GGCGGACTTC TGCTGGAACA GCCTCACTTT CAGCCTGACT 720
CCACTATCTG CATTTAATGT AAACATTCAA GGCTCTTAAT GAAAAAAGTG AACCATTACA 780
TAAATCCAAA ATTTAATTTT AACAAAAGCC AGGCCAGACG CCGTGAGCCT TACAGGCTCG 840
TGCCTATAAG CCCAGCACTT TGGGTGGCCA AGGCAGGAGG ACTGCTTGAG CTCCCAAGTT 900
TGAGACCAGC CTGGCCAACA TAGTGAAACC CTGTCTCTAC TAAAAATACA AAAAGTAGCC 960
AGGCGTGGTG GTGCCCACTG GTGGTCCCAG CTACTCGGGA GGCTGAGGTA GGAGGATCGC 1020
CTGAGCCCAG TGGAGGGGGA GGTTGCAGTG AGCTAAGACT ATACCACTGC ACTCTAGCCT 1080
GGGCGACAGA GAGAGACCCT ATCTCAAAAA ATTAAATTAA ATTTTTAAAA TGCCAGATGA 1140
AAAGGAGGTT GGCTGTTGAA TGAGTAAAAC AAGCATCGGA GGACACAGGG TAAACCTGGC 1200
CAGCCAGGCT GAGGCAGCGT GGGGCTCTGG CCCAGCCTTG CCTGTCCTCC AGGCTGCTCA 1260
GCAGATATCC CATTTGAGGG TGCTGTCCTA AAGCCGGTGT CCCCACATTG GACAGGCCAG 1320
CCTTTTCTTC TCCAAAATGC AGAGACTGAC CCAGGTGCTC TCTCTCCAAG GCTTTGTCCT 1380
ACTCTGGCTT TCTCTGCCCC TTCTCAGCTA CCCCCTCAAC ACCCCCTGCT CCCTCTGGTA 1440
ACCGCATCCT CTCCTTCCCC TCCTCCAGTC TGAGACCCTG CCTTCCTGTC CTGGGGCGGT 1500
GAGACGTGAA TCTGGTGTAT GTGATGGAGA AGGGTCACCT GGTGAGGACT GAGCTCCTTC 1560
TACCCAGGAG ATTCAGCTCA ACGTGACTCT TCTAGAAATC ACCAGAAATG TTCTAACCCA 1620
TTGGTTCCAG 1630