EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS085-00916 
Organism
Homo sapiens 
Tissue/cell
Heart 
Coordinate
chr15:31627140-31628610 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs9920314chr1531627886hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr15:31627687-31627708GGGGCAGGGGGCGGGGGGAGG+6.16
Number of super-enhancer constituents: 43             
IDCoordinateTissue/cell
SE_00626chr15:31625972-31627753Adipose_Nuclei
SE_00626chr15:31627756-31628724Adipose_Nuclei
SE_00955chr15:31626849-31628709Adrenal_Gland
SE_03213chr15:31626899-31628554Brain_Angular_Gyrus
SE_03886chr15:31626731-31627742Brain_Anterior_Caudate
SE_03886chr15:31627778-31636610Brain_Anterior_Caudate
SE_04794chr15:31625728-31662350Brain_Cingulate_Gyrus
SE_05780chr15:31615643-31660953Brain_Hippocampus_Middle
SE_06977chr15:31626602-31629337Brain_Hippocampus_Middle_150
SE_07743chr15:31626497-31648446Brain_Inferior_Temporal_Lobe
SE_09581chr15:31626735-31632849CD14
SE_10960chr15:31626557-31662684CD20
SE_11880chr15:31628141-31628684CD3
SE_17341chr15:31615669-31661138CD4p_CD25-_CD45RAp_Naive
SE_17846chr15:31627800-31662260CD4p_CD25-_CD45ROp_Memory
SE_18423chr15:31625736-31660967CD4p_CD25-_Il17-_PMAstim_Th
SE_19192chr15:31627723-31628911CD4p_CD25-_Il17p_PMAstim_Th17
SE_22346chr15:31627768-31662564CD8_primiary
SE_23077chr15:31628058-31628777Colon_Crypt_1
SE_23726chr15:31628138-31628725Colon_Crypt_2
SE_26685chr15:31626950-31628637Esophagus
SE_30907chr15:31627678-31628992Fetal_Thymus
SE_31418chr15:31626838-31629664Gastric
SE_33429chr15:31627071-31634010H2171
SE_40604chr15:31626796-31650659Left_Ventricle
SE_42098chr15:31626794-31633730Lung
SE_43752chr15:31628410-31631562MM1S
SE_47479chr15:31626902-31628745Pancreas
SE_48083chr15:31626809-31628894Psoas_Muscle
SE_48562chr15:31626825-31632896Right_Atrium
SE_49451chr15:31627856-31628738Right_Ventricle
SE_50055chr15:31626900-31633707Sigmoid_Colon
SE_52342chr15:31626927-31628671Small_Intestine
SE_53298chr15:31626912-31628781Spleen
SE_55094chr15:31627153-31627768Thymus
SE_55094chr15:31627800-31628753Thymus
SE_58529chr15:31616151-31660715Ly1
SE_59212chr15:31615375-31658617Ly3
SE_61508chr15:31616115-31660220Toledo
SE_62250chr15:31615508-31660953Tonsil
SE_65426chr15:31627018-31629579Pancreatic_islets
SE_66929chr15:31627071-31634010H2171
SE_67212chr15:31628410-31631562MM1S
Number: 1             
IDChromosomeStartEnd
GH15I031334chr153162697031629114
Enhancer Sequence
AATAACAGAA ACTCGAACTT GTTTTACTCT TGGCATCAAT CGGGCACTGG GCACAGAAGA 60
AATCCTCACC CAACCAAAAG CTCTGCCATT TGGCCATAAA CACGTATGCC TCCATAGCCA 120
CGTACATGTG TAGAAACACA TATGGGTGTG TGTGTGAGTG GACGTGGCAC CCTGCTCATG 180
CTTGCTGAAT GGGGGAGCAT CCACACCTGG AACATAGTGG CTATGTGGAA CTTCTGATTT 240
CTAGTTCAGT TTTAGATCTT AGGTCCGTCT TCATCCCCAG CAAATGTTAC CAGCTGTTTG 300
TGAGGCAGGC TTTTGGGGGA GACATGAAGT TTGTTCAGTT GAAACTAGGG CTGTGGTGAA 360
GGGGCTATGC CTTCACACCC TGCTGCCCTG CCCAGCAGAG TGACCGGCTC CTGTGTCCTC 420
CACACTGCTT CAGTTCCCCT CCTGATGCAG GGCCAGGCTG TGATCGCCAT TTGCTGTTGG 480
GCATTGTGTG TGTGTGTATG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTA 540
TGGTGGCGGG GCAGGGGGCG GGGGGAGGGC ACAGCATGGC ACCGAGCACC AGAAACACAG 600
CCTTGACCAG TCCCTGGTTT TTACCAACAT CTTTCTGGAC AAACAAGACA GCACACTTGG 660
CAGGGGGAGT ATTCTGTTTA TTGTTCTCCA TTTTTGAAGT TCATCACACA AAAACACTTG 720
CTAACCAGAA ACTTGGCTGC ACTCCGTGGC CATTGGCCAG TCTGTCCCAA GGTGACTTGT 780
TTGGGGAAGC ACTGAAGCTT GATGTCTCAG ATTAAATGTC CTTATGCTGG TGCCACAGGG 840
GTGTGGCCTA CTCTGCATGG ATGGGTGACC CTGGGTCCCC AGGCACAGGG CACAGGCTCG 900
TCTCCTTGAA GCTGGAGCCC ACGCTGCATC ATGAAAGAGC TCTGCAAGAA TTGAAGGCCC 960
AGAGCAAAAA TCGCTTACCA AAGAGCATGT GGCTCAGAGC CTACCTTGGC CTCCTGTCTC 1020
AGGAGAAACT TCTAAAGGTG GAGTTGTGTC ACGTGCTTGT CTCCTGTGAG CACAGGCCAG 1080
GTGGGAGGAA GCTTGGGAGT GGGGAGAGGA TGACGTGGGC TCAGAGGAGC CACGAGCTTC 1140
TCCCCCGACC CCAGCGTACA CTGGACACAC ATGGGAGGTG AGGTGATGCC TGAGCAGCCT 1200
GGCGAGTGGT CAGGGCCCTG GGTGGGGCCT CCTCATTCCC TTTTGGAGCA CTGGCAGCTA 1260
ATGCTTGGGG GGGCCACCAT CCTTTCCCGG TCTGGCCTCG TTGGGGGACA CATCTGTCTT 1320
CCTCCTGGAG TAAGGAGAGC CTGTGAACAA AGCAGTGACC CCAAGACCTA TGGCCACTGG 1380
GGATGGCAGG AGCCTTGTGC TTCCATATGT GGGTCCAAGC TGTGGATGGG GAGGCCAAGT 1440
GTCCTGGCAT GTGGGAGGTG GTCAGGTGCT 1470