EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS048-12011 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr14:91862370-91864840 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ONECUT1MA0679.1chr14:91863393-91863407AAAAAATCAATACT+7.19
ONECUT2MA0756.1chr14:91863393-91863407AAAAAATCAATACT+6.93
ONECUT3MA0757.1chr14:91863393-91863407AAAAAATCAATACT+7.14
ZBED1MA0749.1chr14:91862403-91862416TATATCGCGACAA-6.1
Number of super-enhancer constituents: 42             
IDCoordinateTissue/cell
SE_03973chr14:91861050-91864702Brain_Anterior_Caudate
SE_09196chr14:91856665-91867758CD14
SE_10890chr14:91853239-91874080CD20
SE_11838chr14:91861570-91866075CD3
SE_14423chr14:91861417-91864861CD4_Memory_Primary_7pool
SE_16329chr14:91863089-91864936CD4_Naive_Primary_8pool
SE_16861chr14:91862391-91863015CD4p_CD225int_CD127p_Tmem
SE_16861chr14:91863248-91864807CD4p_CD225int_CD127p_Tmem
SE_17338chr14:91856244-91867630CD4p_CD25-_CD45RAp_Naive
SE_17763chr14:91852838-91886281CD4p_CD25-_CD45ROp_Memory
SE_18257chr14:91853043-91867660CD4p_CD25-_Il17-_PMAstim_Th
SE_19104chr14:91861453-91867601CD4p_CD25-_Il17p_PMAstim_Th17
SE_19998chr14:91858016-91867807CD56
SE_21071chr14:91863003-91867496CD8_Memory_7pool
SE_21656chr14:91862933-91864705CD8_Naive_7pool
SE_21949chr14:91861332-91864885CD8_Naive_8pool
SE_22293chr14:91852641-91884153CD8_primiary
SE_27565chr14:91861495-91866067Esophagus
SE_31363chr14:91861752-91866030Fetal_Thymus
SE_31609chr14:91862966-91866069Gastric
SE_32470chr14:91862971-91865920GM12878
SE_39415chr14:91862434-91863316Jurkat
SE_39415chr14:91863329-91864011Jurkat
SE_39415chr14:91864145-91864871Jurkat
SE_41633chr14:91861443-91863217LNCaP
SE_41633chr14:91863259-91864283LNCaP
SE_41633chr14:91864398-91864799LNCaP
SE_43558chr14:91861466-91867415MM1S
SE_50173chr14:91861588-91866049Sigmoid_Colon
SE_52486chr14:91862575-91867359Small_Intestine
SE_53934chr14:91861761-91866080Spleen
SE_55274chr14:91863042-91864949Thymus
SE_58376chr14:91781648-91886211Ly1
SE_58849chr14:91813006-91886123Ly3
SE_60717chr14:91860252-91886040DHL6
SE_61123chr14:91814842-91881922HBL1
SE_62324chr14:91813043-91886085Tonsil
SE_66290chr14:91862434-91863316Jurkat
SE_66290chr14:91863329-91864011Jurkat
SE_66290chr14:91864145-91864871Jurkat
SE_67160chr14:91861466-91867415MM1S
SE_69082chr14:91860063-91864536H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr149186396191864070
Enhancer Sequence
TTCCTCTCAT TACTAGAAAA ATAAGACGAC AATTATATCG CGACAATTAC ATCTCGAAGG 60
ATCAAGGGGC CCTGGATGCC AAGGCGAAGC AGCAGAGAAT CTCTGCCATT CCCCAAAGAA 120
GAGCTGAATA ACAAAAACTG TTACGAGCCC TGGAGGTGAG CCACGCAGCC GGCTTCACGG 180
AGAGGCAGAG CCTGCCTGGG CAAGTTCTTC TTCAGAAACT CCTTTTGACA AACCAGTGAG 240
AACATCAAAC ATGCTGATCC TGGCATCTAA CACCAAACCC AAGGCAAAGG AGAAACCTCT 300
GTTTTTTCTT TTTAACGACT TGAGAAATCC ATTTCTCTCC TTTCTGTCAC AAAAGGAACT 360
GGTTCCTCCT GCCACTTCCT CCCACTTTGG CGTTTAGGGT ATGTCCATAA AGTGAGCTGT 420
GTTTCCAACC TTCATTCACG CCCGCATCAC TCGATTCCCA CAACACTCAT CACCCACAAG 480
TGCAGCTTTC AATCGGAGCT GAACGAGAGC TAACTAAGAA TGAGCCCGAC AAGCACCGGG 540
AACACCAAGC ACAGCTCACT CGCGGCTTCT GCAAGCTTAA CATTCATCGT TTCAGCCATA 600
ATTTTTCCGG AAGCACAAAT TCAGACCCCT TGCCCTCCGA TCAGGGGATC ACTCAGCTTC 660
CACTCCCAGA AGCTTTGTTG CTTACTTTGT GCTCCCCAAG ATGGGCTCAT AAACACACAT 720
CTCTGTAAAT AAATGGCCAT GAATTAAGAA ACAACTTCAG GAGTTCGAGA CCAGCCTGGG 780
CAACACAGGG AGACTCTGTC TCTACAAAAA ATCAGAAACA TAAATTAGCC AGAAGTGGTG 840
GTGCATGCTG GTAGTCCCAG CTACTCGGGG GGCTGAGGCA GGAGGATTGC TTGAGCCTGG 900
CAGGTCAAGG TCGAGGCTGC AGTAAGCCGT GATCGCACCA CTGCACTCCA GCCTGGGCTA 960
CACAGAGCAA GACCCTGTCA CCAAAAAAAA AAGAAAGAAA GAAAAAAACT TGAGCAAACG 1020
GTGAAAAAAT CAATACTTGA CATGGTAAGA TAACCTGTAT CAGAAACATG ATTCTGGAAC 1080
AAACACCAAT AGGGGAGGGA GAGGGGCCTG GGGGAAGTCC CGATGTGTCA ATGTCCAGAG 1140
GTGGGCAGGT CTCCAAGCAG ACCCTGTGAG GCTGCATGTT CTGAGCATCT GGGCTCGGTG 1200
CTGTGCCCAA CAGGCCCAGG CAAGGGGACA GCCACAGGGG CCTGGGTGGC ATCCCCAACA 1260
CCAGGAGTGA AAGCAAGACT CCTGAGCCAA ACCTCCTTCC CGCAAAGGCT GAGGAAATGA 1320
TGGCCGCTCC TGAAACAGGA GAAAAGCCCC AGCAAATCAA GGTCTTGACT CAAGTCCTAG 1380
AGAAGGAAGC CTCAGAGAAC AGAAAGACTG TGTACACACA CACACTCACA CACACTCTCA 1440
CACTCACACA CTCTCACACT CATACTCACA CACACACATT CTCTCCATCT CCTTGCCCTG 1500
GCTGAACTCC AACTCTGCTA ATTACATCAA ACCCACCTTT CGCCCTCTGC AACACCTGCA 1560
ATTAACCCTG AATCTCTGCT TCCTGCCGCT CTGGGGTGAG GGGTGAAGTC TGAGGCCAGC 1620
TGCTCCCTGT TCCACCCTCC GCCCAACCCC GGAAGTTTCA GAGGTGCCTG AAGCAACCCG 1680
GTCCCTTCCT CTGGGCTCCA GGCTGGTGTG AAGCCGGGTT ATCACGGGAG CCCACACTCC 1740
CAGCTGGGGG GCACACCACA CGCAGCACCC CCACCCCACT GCGGGTGCAG ATCCTGACTG 1800
GCCCTGCCAG CCTTTACAGG ACAGCACGTC CACCTGCAGC AAGTTACCTC CCTACATGAT 1860
TCTAGAAAGC CTGGCTTTTA GAAAGAAGCT TCTCCAAGCA GCTGATGATG AAGAAAACTT 1920
GCAGCTTTCC GGGGCTGTTT CCTGATCTTG CTCCATGAGC CTTGGTTTCC TAATCTATCG 1980
AATGGAGACA GTAATTTCTT CTTTATAATA CCGAAGTAAC AGTGAAAAAT GACGAGGCTC 2040
TAAAGCCCCC AGCATGGGCA CTCAGTAAAG GTTAAGCTCC CTCCCATTCA TCTCTCAGCC 2100
TTTTGATTTG GGCACAGATC TGAGTCCCAC AGTTCCTCGC TGCTATCTGA TATGCCTGGA 2160
CAGCATTTCT TCTGACAACA AAAAGGAGAG AAAAGAAAGG AAAACAAGTC CAACTGGCAC 2220
TCTAACAGCT TACAGAAACC AAATCTGCCT CCCAAGAGGT TTGGGCGTTC AGCACACCAC 2280
CAGGTCCTCA GCCCGTTTGC TTCACCCCTG GCCAACAGTT GAACCACTGA GCTTGTAACA 2340
CCAACACTGG CTGGCATGGT GGCTCACGCC TGTAACCCCA ACACCTTGGG AGGCCAAGGC 2400
AGGAGGATCG CTTGAGCCCA GGAGTTTGAG TAGCCTGGCC AACACAGTGA GACCCCATCT 2460
CTACAAAAAA 2470