EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS026-10805 
Organism
Homo sapiens 
Tissue/cell
CNCC 
Coordinate
chr14:91835040-91837590 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Klf1MA0493.1chr14:91836532-91836543AGCCACACCCT+6.02
Nr2f6(var.2)MA0728.1chr14:91835768-91835783TGAACTCCTGACCTC-6.22
ZNF263MA0528.1chr14:91835300-91835321TCTCCTTTCTCCTCCTTCCTC-6.32
ZNF263MA0528.1chr14:91835301-91835322CTCCTTTCTCCTCCTTCCTCC-6.47
ZNF263MA0528.1chr14:91835297-91835318CCATCTCCTTTCTCCTCCTTC-6.66
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_03973chr14:91835689-91838818Brain_Anterior_Caudate
SE_09196chr14:91823727-91850684CD14
SE_10890chr14:91829021-91845812CD20
SE_11838chr14:91832701-91835371CD3
SE_11838chr14:91835803-91845459CD3
SE_14423chr14:91835737-91842675CD4_Memory_Primary_7pool
SE_16329chr14:91835560-91837081CD4_Naive_Primary_8pool
SE_16861chr14:91832724-91835591CD4p_CD225int_CD127p_Tmem
SE_16861chr14:91835691-91838861CD4p_CD225int_CD127p_Tmem
SE_17338chr14:91829748-91847967CD4p_CD25-_CD45RAp_Naive
SE_17763chr14:91829828-91850361CD4p_CD25-_CD45ROp_Memory
SE_18257chr14:91829503-91852529CD4p_CD25-_Il17-_PMAstim_Th
SE_19104chr14:91834952-91846471CD4p_CD25-_Il17p_PMAstim_Th17
SE_19998chr14:91829148-91846604CD56
SE_21949chr14:91836014-91842734CD8_Naive_8pool
SE_22293chr14:91829667-91846735CD8_primiary
SE_30735chr14:91832884-91837020Fetal_Muscle
SE_31609chr14:91834802-91839930Gastric
SE_32470chr14:91832834-91842229GM12878
SE_39415chr14:91834508-91835670Jurkat
SE_39415chr14:91835888-91837691Jurkat
SE_41633chr14:91834876-91835659LNCaP
SE_41633chr14:91835889-91839882LNCaP
SE_43558chr14:91829346-91847848MM1S
SE_50173chr14:91837188-91843365Sigmoid_Colon
SE_52486chr14:91834826-91835692Small_Intestine
SE_52486chr14:91835847-91836942Small_Intestine
SE_52486chr14:91837253-91846210Small_Intestine
SE_53934chr14:91836012-91836914Spleen
SE_58376chr14:91781648-91886211Ly1
SE_58849chr14:91813006-91886123Ly3
SE_60476chr14:91813015-91845250DHL6
SE_61123chr14:91814842-91881922HBL1
SE_62324chr14:91813043-91886085Tonsil
SE_63268chr14:91820556-91844976GLC16
SE_66290chr14:91834508-91835670Jurkat
SE_66290chr14:91835888-91837691Jurkat
SE_67160chr14:91829346-91847848MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr149183591991837226
Number: 1             
IDChromosomeStartEnd
GH14I091360chr149182650691848271
Enhancer Sequence
GGGCCCCCAA GAGAACCCTG TAGTCAGGAG GGATATTCCA CAGATCTCCT TTGCAGGTGT 60
TGGAACGTCT ACGCTCATGC CACTGATTAA CTCTCCACAG GACACATCTC ACAACCTCTT 120
CCTGGATTTG GCCAGAAGCA GCCCCTGAAT GCACCTCAAC AACTTGATGG CCAAAACAAA 180
AACCACCTGA CGACCTGGCA CTGGCAACCA GCCAACCTCA GGCCCCGTTA CCAGAAACAC 240
CAGACAGTGA AGAGGTTCCA TCTCCTTTCT CCTCCTTCCT CCCTGACATT CATGCGAGGT 300
GGCCAGGACA AGAATTATGA GCATTTCCAG TGGGAGGGAA CAGCCGCAGC ACAATGTCGC 360
TGATCGTTTG CCAGCAGGGC CTGGAGCAAG ACCGGGGTTG GAACCTCAGG CCTGGAGAGC 420
TTCCCTCATA GACACCATCT TCATCACCTC ATGCCCAAAG CCAGAGCACT TTCTACAGCA 480
CAGGCCCGCC CCAAACCTTC AATAACGACT CACGACACAG CCTGTGGCCC AACCCCAGCC 540
AATCACACCC GCCAGGCTGG AGTGCAATGG CGTGATCTCG GCTCACTGCA ACCTCCACAT 600
CCTGGGTTCA AGCAATTCTC CCGCCTCAGC TTCCGAAGTA GCTGGGATTA CAGGCGCCTG 660
CCGTCATGTC CGGCTAATTT TCGTATTTTT GTAAAGATGG GGTTTCATCA TGTTGGCCAG 720
GCTGGTCTTG AACTCCTGAC CTCAGGTGAT CCACCCACCT CGGCCTCCCA AAGTGCTGGG 780
ATCACAGGTG TGACCCACCA TGCCCGGCCA ATTTTCTTAT TTTTTATTCA TTATTATTTT 840
TCTTTTTTTT ACCTCTGGAA CATAGCACAT TTTCTAACAT AGCCACTGAG AGGAAAACCC 900
AAGCAGTGGT TTGTCCTTGC TGCCTGCACA AAGCCCAGGC CCACATGCTT GTAACTCCAT 960
CTGCACAAGA GGCTCTCCTC TCCACCCAGT CCCTCTTCGG GGCGGGGAGT CCTGGCAAAA 1020
CGAGTGGCAA TGAAGTGCTT TTATGTTACG AGGCTGTCAT GTAAAGCTGC TGATAGATTC 1080
AATCCATCTG TTCCACCTCA TTTCGATTAA TCCTGGGATC CCTAGGGCCT GAAACCAACT 1140
GCAATCTGCA CAAGCCCAGG AGCGCCGGCT CCCCTAACAA GGCCACCCGT GTCTCCGTAC 1200
CCAGGGACCA ACTCGGCCCG GCCGAGGCTA CCACGTCATC AGAAAACCCC CTCCCACGGA 1260
ACACTTCCTA ACTGCCTGTC CTTGTGGCTG CATTCACAGA AACAAACATA AGTCGGTTCT 1320
TTGTTCACAG AAAGGAAAAC AAATATTTCC TTTGAGCTGA CCCAGGAGGA GGAGAACCGC 1380
TGGGAAGGAG CACCTGGAAA CTCAAACACC GCAGCATGAG GGCAGAGCCG CTAACTCCTG 1440
CCTCTGCCTG TAACCTACTG TGTGGCCTCA GGCAAGTCAC AGTCCCTCTC TGAGCCACAC 1500
CCTCATCTGT ACCAGGATCA GGACTCCACA GTCTCTAAAG GACTTCAGTC TCCTTCAGAA 1560
GGGGGAAGGG AGGGGCTGGA AAAAGAGACG CTGCTGGCAA GAGAGGCACA GCACATCTTT 1620
ATGGCGTTAA CTCGGCTGCC AGCTCTCACC AGCAGGCAAG TGCCCACGCG TCCAGAAGAA 1680
CTCAGGGAAC CCGGCAGGGA GGGAACCAGA GGATGTTTCA AGTAACCCCA GGAGCTCCTG 1740
CCACCTTCCC TTTAGGGCTG GGTGATGCCC TGGATTGCTC TGTGGGCAGA CCTGTCTTAT 1800
CTGATGCCAG GAAGGGCCTG TTCTGAGCCC CTGAGCCAAA GAAGGGGGCG GGGGGCAGCC 1860
CCAGAAACAC GGGCAGGACA CGGCATTCGA CTCCTTGGAA GAGAACCTCT GCCCATAAAC 1920
AGTAGTTCAG GAACCATTTT ACAAGAGGAA TGCAAGCCGG GTCTCTGCAT CGGGCTTTAG 1980
GAACGACCTG CTGCAGTGAT GCCTCGGCAA CCACAGGTGC GGATGGTGGG GGAGGGGAAG 2040
GCGGGTCAGT AGGTGGACAC ATCCGTGCAT ACAGACCCCA ACAGCAGAGG GATGCTGAGA 2100
ATCTGCATTT TAAAACCAAA AGAGCCATCA AGATTATCCA TAGAGTCAGG AAACTGAGGT 2160
CCGGAGCAAA AAATGACAGA GGCGTAGCCC CACATTCAGG TCTGGAAACC CAGGTCTCCT 2220
TGCACTCCGC CCTAGGGCTC CTTATGCCAT ACCAAGAAGC TTGTATCCAC TCAGCGGTGT 2280
CTGCTGAGTG CATGCCATGC CCTGAGGTGT GTGTTTGGGG TGAGGCAGAA GGACTTCAAG 2340
GATTAGGCTA AGGATGGAGA GAGCAGGACC CTTTCCCCAC AGGACAGCAC CTGCAGCAGT 2400
TCTGGGCTGC CCTTTCCTCT GTCCCTAAGT CCACCCCTCC TGGCTAAAAC GACAGCATCG 2460
GTGCTCCAGT GCTTGGAGTT GATATAAGGG CCCTGATTTT ATGGCCGTGA GGGATCGTAT 2520
GACTGTGACT TCATGGTGGT AGAGTACTTT 2550